Difference between revisions of "Endometrial cancer"

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[[#top|Back to Top]]
 
[[#top|Back to Top]]
 
</div>
 
</div>
{{#lst:Section editor transclusions|gi}}
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{{#lst:Section editor transclusions|gyn}}
<big>Note: the page has systemic regimens for the more general category of RAS wild-type colorectal cancer. Also note that most of the regimens were evaluated on patients tested for KRAS mutations only, and that the definition of wild-type has evolved over time. See individual regimen biomarker eligibility criteria for more details.
+
''Are you looking for a regimen but can't find it here? For placebo or observational studies in this condition, please visit [[Endometrial cancer - null regimens|this page]]. If you still can't find it, please let us know so we can add it!''
*See the [[Colorectal_cancer|'''main colorectal cancer page''']] for general regimens.
 
*See the [[Colon cancer, RAS wild-type|'''RAS wild-type colon cancer page''']] for adjuvant colon cancer regimens.</big>
 
 
{| class="wikitable" style="float:right; margin-right: 5px;"
 
{| class="wikitable" style="float:right; margin-right: 5px;"
 
|-
 
|-
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=Guidelines=
 
=Guidelines=
 
==[http://www.esmo.org/ ESMO]==
 
==[http://www.esmo.org/ ESMO]==
*'''2016:''' [http://annonc.oxfordjournals.org/content/27/8/1386.full.pdf+html ESMO consensus guidelines for the management of patients with metastatic colorectal cancer.] [https://pubmed.ncbi.nlm.nih.gov/27380959 PubMed]
+
*'''2022:''' Oaknin et al. [https://doi.org/10.1016/j.annonc.2022.05.009 Endometrial cancer: ESMO Clinical Practice Guideline for diagnosis, treatment and follow-up]
*'''2013:''' [http://annonc.oxfordjournals.org/content/24/suppl_6/vi73.full.pdf+html Familial risk-colorectal cancer: ESMO Clinical Practice Guidelines.] [https://pubmed.ncbi.nlm.nih.gov/23813931 PubMed]
+
===Older===
==[http://www.jsccr.jp/en/index.html Japanese Society for Cancer of the Colon and Rectum]==
+
*'''2016:''' Colombo et al. [https://www.esmo.org/Guidelines/Gynaecological-Cancers/ESMO-ESGO-ESTRO-Consensus-Conference-on-Endometrial-Cancer ESMO-ESGO-ESTRO Consensus Conference on Endometrial Cancer: diagnosis, treatment and follow-up]
*'''2016:''' [https://doi.org/10.1007/s10147-017-1101-6 Japanese Society for Cancer of the Colon and Rectum (JSCCR) guidelines 2016 for the treatment of colorectal cancer] [https://pubmed.ncbi.nlm.nih.gov/28349281 PubMed]
 
 
==[https://www.nccn.org/ NCCN]==
 
==[https://www.nccn.org/ NCCN]==
*[https://www.nccn.org/professionals/physician_gls/pdf/colon.pdf NCCN Guidelines - Colon Cancer]
+
*[https://www.nccn.org/professionals/physician_gls/pdf/uterine.pdf NCCN Guidelines - Uterine Neoplasms]
=Perioperative therapy for oligometastatic disease=
+
=Adjuvant therapy=
==FOLFIRI {{#subobject:a051ec|Regimen=1}}==
+
==Carboplatin & Paclitaxel (CP) {{#subobject:b9c21f|Regimen=1}}==
FOLFIRI: '''<u>FOL</u>'''inic acid, '''<u>F</u>'''luorouracil, '''<u>IRI</u>'''notecan
 
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen {{#subobject:49d215|Variant=1}}===
+
===Regimen variant #1, 5/175 x 4 {{#subobject:6bc3c0|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
Line 33: Line 29:
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
|-
 
|-
|[https://doi.org/10.1200/JCO.2012.44.8308 Ye et al. 2013 (Fudan 2012-03)]
+
|[https://doi.org/10.1016/S1470-2045(18)30079-2 de Boer et al. 2018 (PORTEC-3)]
|2008-2011 (NR)
+
|2006-2013
| style="background-color:#1a9851" |Phase 3 (C)
+
|style="background-color:#1a9851"|Phase 3 (E-esc)
|[[#FOLFIRI_.26_Cetuximab|FOLFIRI & Cetuximab]]
+
|[[Complex_multipart_regimens#PORTEC-3|See link]]
| style="background-color:#d73027" |Inferior OS
+
| style="background-color:#91cf60" |[[Complex_multipart_regimens#PORTEC-3|See link]]
 
|-
 
|-
 
|}
 
|}
''Note: this trial was only open to KRAS wild-type patients with synchronous liver-confined unresectable metastases.''
+
<div class="toccolours" style="background-color:#cbd5e8">
 +
====Preceding treatment====
 +
**[[Surgery#Endometrial_cancer_surgery|Surgery]], then [[#Cisplatin_.26_RT|Cisplatin & RT]]
 +
</div>
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
*[[Fluorouracil (5-FU)]] 400 mg/m<sup>2</sup> IV bolus once on day 1, then 2400 mg/m<sup>2</sup> IV continuous infusion over 46 hours (total dose per cycle: 2800 mg/m<sup>2</sup>)
+
*[[Carboplatin (Paraplatin)]] AUC 5 IV once on day 1
*[[Folinic acid (Leucovorin)]] 400 mg/m<sup>2</sup> IV once on day 1
+
*[[Paclitaxel (Taxol)]] 175 mg/m<sup>2</sup> IV once on day 1
*[[Irinotecan (Camptosar)]] 180 mg/m<sup>2</sup> IV once on day 1
+
'''21-day cycle for 4 cycles'''
'''14-day cycles until lesions deemed resectable or up to 12 cycles'''
+
</div></div><br>
</div></div>
 
===References===
 
#'''Fudan 2012-03:''' Ye LC, Liu TS, Ren L, Wei Y, Zhu DX, Zai SY, Ye QH, Yu Y, Xu B, Qin XY, Xu J. Randomized controlled trial of cetuximab plus chemotherapy for patients with KRAS wild-type unresectable colorectal liver-limited metastases. J Clin Oncol. 2013 Jun 1;31(16):1931-8. Epub 2013 Apr 8. [https://doi.org/10.1200/JCO.2012.44.8308 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/23569301 PubMed] NCT01564810
 
==FOLFIRI & Cetuximab {{#subobject:a051ec|Regimen=1}}==
 
FOLFIRI & Cetuximab: '''<u>FOL</u>'''inic acid, '''<u>F</u>'''luorouracil, '''<u>IRI</u>'''notecan, Cetuximab
 
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen variant #1, weekly cetuximab {{#subobject:8f47f9|Variant=1}}===
+
===Regimen variant #2, 6/175 x 6 {{#subobject:6bc5c0|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
Line 61: Line 55:
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
|-
 
|-
|[https://doi.org/10.1200/JCO.2012.44.8308 Ye et al. 2013 (Fudan 2012-03)]
+
|[https://doi.org/10.1056/NEJMoa1813181 Matei et al. 2019 (GOG 258)]
|2008-2011 (NR)
+
|2009-2014
| style="background-color:#1a9851" |Phase 3 (E-esc)
+
| style="background-color:#1a9851" |Phase 3 (C)
|[[#FOLFIRI|FOLFIRI]]
+
|[[#Cisplatin_.26_RT|Cisplatin & RT]], then [[#Carboplatin_.26_Paclitaxel_.28CP.29|CP]] x 4
| style="background-color:#1a9850" |Superior OS<br>Median OS: 30.9 vs 21 mo<br>(HR 0.54, 95% CI 0.33-0.88)
+
| style="background-color:#ffffbf" |Did not meet primary endpoint of RFS
 
|-
 
|-
 
|}
 
|}
''Note: this trial was only open to KRAS wild-type patients with synchronous liver-confined unresectable metastases.''
+
<div class="toccolours" style="background-color:#cbd5e8">
<div class="toccolours" style="background-color:#fdcdac">
+
====Preceding treatment====
====Biomarker eligibility criteria====
+
*[[Surgery#Hysterectomy|Hysterectomy]] and [[Surgery#Bilateral_salpingo-oophorectomy|bilateral salpingo-oophorectomy]], within 8 weeks
*Wild-type KRAS, Wild-type NRAS
 
 
</div>
 
</div>
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
*[[Fluorouracil (5-FU)]] 400 mg/m<sup>2</sup> IV bolus once on day 1, then 2400 mg/m<sup>2</sup> IV continuous infusion over 46 hours (total dose per cycle: 2800 mg/m<sup>2</sup>)
+
*[[Carboplatin (Paraplatin)]] AUC 6 IV once on day 1
*[[Folinic acid (Leucovorin)]] 400 mg/m<sup>2</sup> IV once on day 1
+
*[[Paclitaxel (Taxol)]] 175 mg/m<sup>2</sup> IV once on day 1
*[[Irinotecan (Camptosar)]] 180 mg/m<sup>2</sup> IV once on day 1
+
'''21-day cycle for 6 cycles'''
====Targeted therapy====
+
</div></div>
*[[Cetuximab (Erbitux)]] as follows, '''given first''':
+
===References===
**Cycle 1: 400 mg/m<sup>2</sup> IV once on day 1, then 250 mg/m<sup>2</sup> IV once on day 8
+
# '''PORTEC-3:''' de Boer SM, Powell ME, Mileshkin L, Katsaros D, Bessette P, Haie-Meder C, Ottevanger PB, Ledermann JA, Khaw P, Colombo A, Fyles A, Baron MH, Jürgenliemk-Schulz IM, Kitchener HC, Nijman HW, Wilson G, Brooks S, Carinelli S, Provencher D, Hanzen C, Lutgens LCHW, Smit VTHBM, Singh N, Do V, D'Amico R, Nout RA, Feeney A, Verhoeven-Adema KW, Putter H, Creutzberg CL; PORTEC study group. Adjuvant chemoradiotherapy versus radiotherapy alone for women with high-risk endometrial cancer (PORTEC-3): final results of an international, open-label, multicentre, randomised, phase 3 trial. Lancet Oncol. 2018 Mar;19(3):295-309. Epub 2018 Feb 12. [https://doi.org/10.1016/S1470-2045(18)30079-2 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5840256/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/29449189 PubMed] NCT00411138
**Cycles 2 up to 12: 250 mg/m<sup>2</sup> IV once per day on days 1 & 8
+
## '''Update:''' de Boer SM, Powell ME, Mileshkin L, Katsaros D, Bessette P, Haie-Meder C, Ottevanger PB, Ledermann JA, Khaw P, D'Amico R, Fyles A, Baron MH, Jürgenliemk-Schulz IM, Kitchener HC, Nijman HW, Wilson G, Brooks S, Gribaudo S, Provencher D, Hanzen C, Kruitwagen RF, Smit VTHBM, Singh N, Do V, Lissoni A, Nout RA, Feeney A, Verhoeven-Adema KW, Putter H, Creutzberg CL; PORTEC Study Group. Adjuvant chemoradiotherapy versus radiotherapy alone in women with high-risk endometrial cancer (PORTEC-3): patterns of recurrence and post-hoc survival analysis of a randomised phase 3 trial. Lancet Oncol. 2019 Sep;20(9):1273-1285. Epub 2019 Jul 22. Erratum in: Lancet Oncol. 2019 Sep;20(9):e468. [https://doi.org/10.1016/S1470-2045(19)30395-X link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/31345626 PubMed]
'''14-day cycles until lesions deemed resectable or up to 12 cycles'''
+
# '''GOG 258:''' Matei D, Filiaci V, Randall ME, Mutch D, Steinhoff MM, DiSilvestro PA, Moxley KM, Kim YM, Powell MA, O'Malley DM, Spirtos NM, Small W Jr, Tewari KS, Richards WE, Nakayama J, Matulonis UA, Huang HQ, Miller DS. Adjuvant chemotherapy plus radiation for locally advanced endometrial cancer. N Engl J Med. 2019 Jun 13;380(24):2317-2326. [https://doi.org/10.1056/NEJMoa1813181 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/31189035 PubMed] NCT00942357
</div></div><br>
+
# '''JGOG2043:''' Nomura H, Aoki D, Michimae H, Mizuno M, Nakai H, Arai M, Sasagawa M, Ushijima K, Sugiyama T, Saito M, Tokunaga H, Matoda M, Nakanishi T, Watanabe Y, Takahashi F, Saito T, Yaegashi N; Japanese Gynecologic Oncology Group. Effect of Taxane Plus Platinum Regimens vs Doxorubicin Plus Cisplatin as Adjuvant Chemotherapy for Endometrial Cancer at a High Risk of Progression: A Randomized Clinical Trial. JAMA Oncol. 2019 Jun 1;5(6):833-840. Epub 2019 Mar 21.  [https://jamanetwork.com/journals/jamaoncology/fullarticle/2728809 link to original article] '''contains dosing details in manuscript''' [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6567838/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/30896757 PubMed] UMIN000000522
 +
# '''KEYNOTE-B21:''' NCT04634877
 +
==CIM {{#subobject:ac4dbb|Regimen=1}}==
 +
CIM: '''<u>C</u>'''isplatin, '''<u>I</u>'''fosfamide, '''<u>M</u>'''esna
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen variant #2, bi-weekly cetuximab {{#subobject:49d215|Variant=1}}===
+
===Regimen {{#subobject:f97ea4|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
Line 93: Line 89:
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
|-
 
|-
|[https://doi.org/10.1200/JCO.2012.44.8308 Ye et al. 2013 (Fudan 2012-03)]
+
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2752331 Wolfson et al. 2007 (GOG 150)]
|2008-2011 (NR)
+
|1993-2005
| style="background-color:#1a9851" |Phase 3 (E-esc)
+
|style="background-color:#1a9851"|Phase 3 (E-switch-ooc)
|[[#FOLFIRI|FOLFIRI]]
+
|[[#Whole_abdominal_radiation_.28WAI.29|Whole abdominal irradiation]]
| style="background-color:#1a9850" |Superior OS<br>Median OS: 30.9 vs 21 mo<br>(HR 0.54, 95% CI 0.33-0.88)
+
|style="background-color:#d9ef8b"|Might have superior OS<sup>1</sup><br>Median OS: 48 vs 24 mo<br>(HR 0.71, 95% CI 0.48-1.05)
 
|-
 
|-
 
|}
 
|}
''Note: this trial was only open to KRAS wild-type patients with synchronous liver-confined unresectable metastases.''
+
''<sup>1</sup>Median OS is not reported in the paper and is estimated from the K-M curve.''
 +
<div class="toccolours" style="background-color:#cbd5e8">
 +
====Preceding treatment====
 +
*[[Surgery#Endometrial_cancer_surgery|Surgery]]
 +
</div>
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
*[[Fluorouracil (5-FU)]] 400 mg/m<sup>2</sup> IV bolus once on day 1, then 2400 mg/m<sup>2</sup> IV continuous infusion over 46 hours (total dose per cycle: 2800 mg/m<sup>2</sup>)
+
*[[Cisplatin (Platinol)]] 20 mg/m<sup>2</sup> IV once per day on days 1 to 4, '''given first, at an infusion rate of approximately 1 mg/min'''
*[[Folinic acid (Leucovorin)]] 400 mg/m<sup>2</sup> IV once on day 1
+
*[[Ifosfamide (Ifex)]] 1500 mg/m<sup>2</sup> IV over 60 minutes once per day on days 1 to 4, '''given second, with mesna'''
*[[Irinotecan (Camptosar)]] 180 mg/m<sup>2</sup> IV once on day 1
+
====Supportive therapy====
====Targeted therapy====
+
*[[Mesna (Mesnex)]] 120 mg/m<sup>2</sup> IV over 15 minutes once on day 1, then 1500 mg/m<sup>2</sup>/day IV continuous infusion over 96 hours, '''given second, with [[Ifosfamide (Ifex)]]'''
*[[Cetuximab (Erbitux)]] 500 mg/m<sup>2</sup> IV once on day 1, '''given first'''
+
*Suggested hydration: 1 liter of NS or 1/2 NS over several hours once per day on days 1 to 4, prior to chemotherapy
'''14-day cycles until lesions deemed resectable or up to 12 cycles'''
+
'''21-day cycle for 3 cycles'''
 
</div></div>
 
</div></div>
 
===References===
 
===References===
#'''Fudan 2012-03:''' Ye LC, Liu TS, Ren L, Wei Y, Zhu DX, Zai SY, Ye QH, Yu Y, Xu B, Qin XY, Xu J. Randomized controlled trial of cetuximab plus chemotherapy for patients with KRAS wild-type unresectable colorectal liver-limited metastases. J Clin Oncol. 2013 Jun 1;31(16):1931-8. Epub 2013 Apr 8. [https://doi.org/10.1200/JCO.2012.44.8308 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/23569301 PubMed] NCT01564810
+
# '''GOG 150:''' Wolfson AH, Brady MF, Rocereto T, Mannel RS, Lee YC, Futoran RJ, Cohn DE, Ioffe OB. A Gynecologic Oncology Group randomized phase III trial of whole abdominal irradiation (WAI) vs cisplatin-ifosfamide and mesna (CIM) as post-surgical therapy in stage I-IV carcinosarcoma (CS) of the uterus. Gynecol Oncol. 2007 Nov;107(2):177-85. Epub 2007 Sep 5. [https://www.gynecologiconcology-online.net/article/S0090-8258(07)00567-7 link to original article] '''contains dosing details in manuscript''' [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2752331/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/17822748 PubMed] NCT00002546
==mFOLFOX6 {{#subobject:8fcd39|Regimen=1}}==
+
==Cisplatin & Doxorubicin {{#subobject:4d10f0|Regimen=1}}==
mFOLFOX6: '''<u>m</u>'''odified '''<u>FOL</u>'''inic acid, '''<u>F</u>'''luorouracil, '''<u>OX</u>'''aliplatin
+
CD: '''<u>C</u>'''isplatin & '''<u>D</u>'''oxorubicin
 +
<br>AP: '''<u>A</u>'''driamycin (Doxorubicin) & '''<u>P</u>'''latinol (Cisplatin)
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen variant #1, 400/2800/85, resectable or suboptimally resectable {{#subobject:17252e|Variant=1}}===
+
===Regimen variant #1, 50/45, capped BSA {{#subobject:ef532f|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
Line 123: Line 124:
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
|-
 
|-
|[https://doi.org/10.1016/S1470-2045(14)70105-6 Primrose et al. 2014 (New EPOC)]
+
|[http://www.gynecologiconcology-online.net/article/S0090-8258(08)00938-4 Homesley et al. 2008 (GOG 184)]
|2007-2012 (F)
+
|2000-2004
| style="background-color:#1a9851" |Phase 3 (C)
+
|style="background-color:#1a9851"|Phase 3 (C)
|[[#mFOLFOX6_.26_Cetuximab|mFOLFOX6 & Cetuximab]]
+
|[[#Cisplatin.2C_Doxorubicin.2C_Paclitaxel_99|CDP]]
| style="background-color:#ffffbf" |Did not meet primary endpoint of PFS<sup>1</sup><br>Median PFS: 22.2 vs 15.5 mo<br>(HR 0.85, 95% CI 0.64-1.15)
+
|style="background-color:#ffffbf"|Did not meet primary endpoint of RFS
 
|-
 
|-
 
|}
 
|}
''<sup>1</sup>Reported efficacy is based on the 2020 update.''<br>
+
''Note: Treatment was to start within 8 weeks of completion of RT.''
''Note: this trial was only open to KRAS wild-type patients with resectable or suboptimally resectable colorectal liver metastases.''
+
<div class="toccolours" style="background-color:#cbd5e8">
<div class="toccolours" style="background-color:#fdcdac">
+
====Preceding treatment====
====Biomarker eligibility criteria====
+
*[[Surgery#Endometrial_cancer_surgery|Surgery]], then [[#Radiation_therapy|RT]]
*KRAS wild-type
 
 
</div>
 
</div>
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
*[[Folinic acid (Leucovorin)]] 400 mg/m<sup>2</sup> IV once on day 1
+
*[[Cisplatin (Platinol)]] 50 mg/m<sup>2</sup> (maximum dose of 100 mg) IV once on day 1, '''given second'''
*[[Fluorouracil (5-FU)]] 400 mg/m<sup>2</sup> IV bolus once on day 1, then 2400 mg/m<sup>2</sup> IV continuous infusion over 46 hours (total dose per cycle: 2800 mg/m<sup>2</sup>)
+
*[[Doxorubicin (Adriamycin)]] 45 mg/m<sup>2</sup> (maximum dose of 90 mg) IV once on day 1, '''given first'''
*[[Oxaliplatin (Eloxatin)]] 85 mg/m<sup>2</sup> IV once on day 1
+
====Supportive therapy====
'''14-day cycle for 6 cycles, then surgery, then 14-day cycle for 6 cycles'''
+
*G-CSF, ONE of the following:
 +
**[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day on days 2 to 11, or until ANC increases to 10,000/uL
 +
**[[Pegfilgrastim (Neulasta)]] 6 mg SC once on day 2
 +
*[[Dexamethasone (Decadron)]] 10 mg IV once on day 1, prior to chemotherapy
 +
*[[:Category:Serotonin_5-HT3_antagonists|5-HT3 antagonist]]
 +
'''21-day cycle for 6 cycles'''
 
</div></div><br>
 
</div></div><br>
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen variant #2, 400/2800/85, unresectable {{#subobject:e190fa|Variant=1}}===
+
===Regimen variant #2, 50/60 x 6 {{#subobject:5fef3b|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
Line 152: Line 157:
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
|-
 
|-
|[https://doi.org/10.1200/JCO.2012.44.8308 Ye et al. 2013 (Fudan 2012-03)]
+
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6567838/ Nomura et al. 2019 (JGOG2043)]
|2008-2011 (NR)
+
|2006-2011
| style="background-color:#1a9851" |Phase 3 (C)
+
|style="background-color:#1a9851"|Phase 3 (C)
|[[#mFOLFOX6_.26_Cetuximab|mFOLFOX6 & Cetuximab]]
+
|1. [[#Carboplatin_.26_Paclitaxel_.28CP.29|Carboplatin & Paclitaxel]]<br> 2. [[#Cisplatin_.26_Docetaxel_.28DC.29_99|Cisplatin & Docetaxel]]
| style="background-color:#d73027" |Inferior OS
+
| style="background-color:#ffffbf" |Did not meet primary endpoint of PFS
 
|-
 
|-
 
|}
 
|}
''Note: this trial was only open to KRAS wild-type patients with synchronous liver-confined unresectable metastases.''
+
<div class="toccolours" style="background-color:#cbd5e8">
 +
====Preceding treatment====
 +
*[[Surgery#Endometrial_cancer_surgery|Surgery]]
 +
</div>
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
*[[Folinic acid (Leucovorin)]] 400 mg/m<sup>2</sup> IV once on day 1
+
*[[Cisplatin (Platinol)]] 50 mg/m<sup>2</sup> IV once on day 1, '''given second'''
*[[Fluorouracil (5-FU)]] 400 mg/m<sup>2</sup> IV bolus once on day 1, then 2400 mg/m<sup>2</sup> IV continuous infusion over 46 hours (total dose per cycle: 2800 mg/m<sup>2</sup>)
+
*[[Doxorubicin (Adriamycin)]] 60 mg/m<sup>2</sup> IV once on day 1, '''given first'''
*[[Oxaliplatin (Eloxatin)]] 85 mg/m<sup>2</sup> IV once on day 1
+
'''21-day cycle for 6 cycles'''
'''14-day cycles until lesions deemed resectable or up to 12 cycles'''
+
</div></div><br>
</div></div>
 
===References===
 
#'''Fudan 2012-03:''' Ye LC, Liu TS, Ren L, Wei Y, Zhu DX, Zai SY, Ye QH, Yu Y, Xu B, Qin XY, Xu J. Randomized controlled trial of cetuximab plus chemotherapy for patients with KRAS wild-type unresectable colorectal liver-limited metastases. J Clin Oncol. 2013 Jun 1;31(16):1931-8. Epub 2013 Apr 8. [https://doi.org/10.1200/JCO.2012.44.8308 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/23569301 PubMed] NCT01564810
 
#'''New EPOC:''' Primrose J, Falk S, Finch-Jones M, Valle J, O'Reilly D, Siriwardena A, Hornbuckle J, Peterson M, Rees M, Iveson T, Hickish T, Butler R, Stanton L, Dixon E, Little L, Bowers M, Pugh S, Garden OJ, Cunningham D, Maughan T, Bridgewater J. Systemic chemotherapy with or without cetuximab in patients with resectable colorectal liver metastasis: the New EPOC randomised controlled trial. Lancet Oncol. 2014 May;15(6):601-11. Epub 2014 Apr 7. Erratum in: Lancet Oncol. 2014 Jun;15(7):e253. [https://doi.org/10.1016/S1470-2045(14)70105-6 link to original article] [https://pubmed.ncbi.nlm.nih.gov/24717919 PubMed] ISRCTN22944367
 
##'''Update:''' Bridgewater JA, Pugh SA, Maishman T, Eminton Z, Mellor J, Whitehead A, Stanton L, Radford M, Corkhill A, Griffiths GO, Falk S, Valle JW, O'Reilly D, Siriwardena AK, Hornbuckle J, Rees M, Iveson TJ, Hickish T, Garden OJ, Cunningham D, Maughan TS, Primrose JN; New EPOC investigators. Systemic chemotherapy with or without cetuximab in patients with resectable colorectal liver metastasis (New EPOC): long-term results of a multicentre, randomised, controlled, phase 3 trial. Lancet Oncol. 2020 Mar;21(3):398-411. Epub 2020 Jan 31. [https://doi.org/10.1016/s1470-2045(19)30798-3 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/pmc7052737/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/32014119 PubMed]
 
==mFOLFOX6 & Cetuximab {{#subobject:8fcd39|Regimen=1}}==
 
mFOLFOX6 & Cetuximab: '''<u>m</u>'''odified '''<u>FOL</u>'''inic acid, '''<u>F</u>'''luorouracil, '''<u>OX</u>'''aliplatin, Cetuximab
 
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen variant #1, weekly cetuximab {{#subobject:dcf5ee|Variant=1}}===
+
===Regimen variant #3, 50/60 x 8 {{#subobject:5bab3b|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
Line 182: Line 183:
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
|-
 
|-
|[https://doi.org/10.1200/JCO.2012.44.8308 Ye et al. 2013 (Fudan 2012-03)]
+
|[https://doi.org/10.1200/jco.2004.00.7617 Randall et al. 2006 (GOG 122)]
|2008-2011 (NR)
+
|1992-2000
| style="background-color:#1a9851" |Phase 3 (E-esc)
+
|style="background-color:#1a9851"|Phase 3 (E-switch-ooc)
|[[#mFOLFOX6|mFOLFOX6]]
+
|[[#Whole_abdominal_radiation_.28WAI.29|Whole abdominal irradiation]]
| style="background-color:#1a9850" |Superior OS<br>Median OS: 30.9 vs 21 mo<br>(HR 0.54, 95% CI 0.33-0.88)
+
|style="background-color:#1a9850"|Superior OS<br>OS60: 55% vs 42%<br>(aHR 0.68, 95% CI 0.52-0.89)
 
|-
 
|-
 
|}
 
|}
''Note: this trial was only open to KRAS wild-type patients with synchronous liver-confined unresectable metastases.''
+
<div class="toccolours" style="background-color:#cbd5e8">
<div class="toccolours" style="background-color:#fdcdac">
+
====Preceding treatment====
====Biomarker eligibility criteria====
+
*[[Surgery#Endometrial_cancer_surgery|Surgery]], with optimal debulking
*Wild-type KRAS, Wild-type NRAS
 
 
</div>
 
</div>
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
*[[Fluorouracil (5-FU)]] 400 mg/m<sup>2</sup> IV bolus once on day 1, then 2400 mg/m<sup>2</sup> IV continuous infusion over 46 hours (total dose per cycle: 2800 mg/m<sup>2</sup>)
+
*[[Cisplatin (Platinol)]] 50 mg/m<sup>2</sup> IV once on day 1
*[[Folinic acid (Leucovorin)]] 400 mg/m<sup>2</sup> IV once on day 1
+
*[[Doxorubicin (Adriamycin)]] as follows:
*[[Oxaliplatin (Eloxatin)]] 85 mg/m<sup>2</sup> IV once on day 1
+
**Cycles 1 to 7: 60 mg/m<sup>2</sup> IV once on day 1
====Targeted therapy====
+
====Supportive therapy====
*[[Cetuximab (Erbitux)]] as follows, '''given first''':
+
*Normal saline at 500 mL/H for 2 hours prior to and after [[Cisplatin (Platinol)]]
**Cycle 1: 400 mg/m<sup>2</sup> IV once on day 1, then 250 mg/m<sup>2</sup> IV once on day 8
+
'''21-day cycle for 8 cycles'''
**Cycles 2 up to 12: 250 mg/m<sup>2</sup> IV once per day on days 1 & 8
+
</div></div>
'''14-day cycles until lesions deemed resectable or up to 12 cycles'''
+
===References===
</div></div><br>
+
# '''GOG 122:''' Randall ME, Filiaci VL, Muss H, Spirtos NM, Mannel RS, Fowler J, Thigpen JT, Benda JA; Gynecologic Oncology Group. Randomized phase III trial of whole-abdominal irradiation versus doxorubicin and cisplatin chemotherapy in advanced endometrial carcinoma: a Gynecologic Oncology Group study. J Clin Oncol. 2006 Jan 1;24(1):36-44. Epub 2005 Dec 5. [https://doi.org/10.1200/jco.2004.00.7617 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/16330675 PubMed]
 +
# '''GOG 184:''' Homesley HD, Filiaci V, Gibbons SK, Long HJ, Cella D, Spirtos NM, Morris RT, DeGeest K, Lee R, Montag A. A randomized phase III trial in advanced endometrial carcinoma of surgery and volume directed radiation followed by cisplatin and doxorubicin with or without paclitaxel: A Gynecologic Oncology Group study. Gynecol Oncol. 2009 Mar;112(3):543-52. Epub 2008 Dec 23. [http://www.gynecologiconcology-online.net/article/S0090-8258(08)00938-4 link to original article] '''contains dosing details in manuscript''' [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4459781/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/19108877 PubMed] NCT00006011
 +
## '''Update:''' Spirtos NM, Enserro D, Homesley HD, Gibbons SK, Cella D, Morris RT, DeGeest K, Lee RB, Miller DS. The addition of paclitaxel to doxorubicin and cisplatin and volume-directed radiation does not improve overall survival (OS) or long-term recurrence-free survival (RFS) in advanced endometrial cancer (EC): a randomized phase III NRG/Gynecologic Oncology Group (GOG) study. Gynecol Oncol. 2019 Jul;154(1):13-21. Epub 2019 Apr 30. [https://doi.org/10.1016/j.ygyno.2019.03.240 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6852648/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/31053405 PubMed]
 +
# '''JGOG2043:''' Nomura H, Aoki D, Michimae H, Mizuno M, Nakai H, Arai M, Sasagawa M, Ushijima K, Sugiyama T, Saito M, Tokunaga H, Matoda M, Nakanishi T, Watanabe Y, Takahashi F, Saito T, Yaegashi N; Japanese Gynecologic Oncology Group. Effect of Taxane Plus Platinum Regimens vs Doxorubicin Plus Cisplatin as Adjuvant Chemotherapy for Endometrial Cancer at a High Risk of Progression: A Randomized Clinical Trial. JAMA Oncol. 2019 Jun 1;5(6):833-840. Epub 2019 Mar 21.  [https://jamanetwork.com/journals/jamaoncology/fullarticle/2728809 link to original article] '''contains dosing details in manuscript''' [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6567838/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/30896757 PubMed] UMIN000000522
 +
==Cisplatin & RT {{#subobject:4d8gh0|Regimen=1}}==
 +
Cisplatin & RT: Cisplatin & '''<u>R</u>'''adiation '''<u>T</u>'''herapy
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen variant #2, bi-weekly cetuximab {{#subobject:e190fa|Variant=1}}===
+
===Regimen {{#subobject:4bfa1d|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
Line 214: Line 219:
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
|-
 
|-
|[https://doi.org/10.1200/JCO.2012.44.8308 Ye et al. 2013 (Fudan 2012-03)]
+
|[https://doi.org/10.1016/S1470-2045(18)30079-2 de Boer et al. 2018 (PORTEC-3)]
|2008-2011 (NR)
+
|2006-2013
| style="background-color:#1a9851" |Phase 3 (E-esc)
+
|style="background-color:#1a9851"|Phase 3 (E-esc)
|[[#mFOLFOX6|mFOLFOX6]]
+
|[[Complex_multipart_regimens#PORTEC-3|See link]]
| style="background-color:#1a9850" |Superior OS<br>Median OS: 30.9 vs 21 mo<br>(HR 0.54, 95% CI 0.33-0.88)
+
| style="background-color:#91cf60" |[[Complex_multipart_regimens#PORTEC-3|See link]]
 
|-
 
|-
 
|}
 
|}
''Note: this trial was only open to KRAS wild-type patients with synchronous liver-confined unresectable metastases.''
+
''Note: in PORTEC-3, radiation is to start within 4 to 6 weeks after surgery, and no later than 8 weeks; reported efficacy is based on the 2019 update.''
 +
<div class="toccolours" style="background-color:#cbd5e8">
 +
====Preceding treatment====
 +
*[[Surgery#Endometrial_cancer_surgery|Surgery]]
 +
</div>
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
*[[Fluorouracil (5-FU)]] 400 mg/m<sup>2</sup> IV bolus once on day 1, then 2400 mg/m<sup>2</sup> IV continuous infusion over 46 hours (total dose per cycle: 2800 mg/m<sup>2</sup>)
+
*[[Cisplatin (Platinol)]] 50 mg/m<sup>2</sup> IV once on day 1
*[[Folinic acid (Leucovorin)]] 400 mg/m<sup>2</sup> IV once on day 1
+
'''21-day cycle for 2 cycles'''
*[[Oxaliplatin (Eloxatin)]] 85 mg/m<sup>2</sup> IV once on day 1
+
====Radiotherapy====
====Targeted therapy====
+
*[[External beam radiotherapy]] to the pelvis, 1.8 Gy x 27 fractions (total dose: 48.6 Gy)
*[[Cetuximab (Erbitux)]] 500 mg/m<sup>2</sup> IV once on day 1, '''given first'''
+
'''5.5-week course'''
'''14-day cycles until lesions deemed resectable or up to 12 cycles'''
+
</div>
 +
<div class="toccolours" style="background-color:#cbd5e7">
 +
====Subsequent treatment====
 +
*[[#Carboplatin_.26_Paclitaxel_.28CP.29|Carboplatin & Paclitaxel]] x 4
 
</div></div>
 
</div></div>
 
===References===
 
===References===
#'''Fudan 2012-03:''' Ye LC, Liu TS, Ren L, Wei Y, Zhu DX, Zai SY, Ye QH, Yu Y, Xu B, Qin XY, Xu J. Randomized controlled trial of cetuximab plus chemotherapy for patients with KRAS wild-type unresectable colorectal liver-limited metastases. J Clin Oncol. 2013 Jun 1;31(16):1931-8. Epub 2013 Apr 8. [https://doi.org/10.1200/JCO.2012.44.8308 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/23569301 PubMed] NCT01564810
+
# '''PORTEC-3:''' de Boer SM, Powell ME, Mileshkin L, Katsaros D, Bessette P, Haie-Meder C, Ottevanger PB, Ledermann JA, Khaw P, Colombo A, Fyles A, Baron MH, Jürgenliemk-Schulz IM, Kitchener HC, Nijman HW, Wilson G, Brooks S, Carinelli S, Provencher D, Hanzen C, Lutgens LCHW, Smit VTHBM, Singh N, Do V, D'Amico R, Nout RA, Feeney A, Verhoeven-Adema KW, Putter H, Creutzberg CL; PORTEC study group. Adjuvant chemoradiotherapy versus radiotherapy alone for women with high-risk endometrial cancer (PORTEC-3): final results of an international, open-label, multicentre, randomised, phase 3 trial. Lancet Oncol. 2018 Mar;19(3):295-309. Epub 2018 Feb 12. [https://doi.org/10.1016/S1470-2045(18)30079-2 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5840256/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/29449189 PubMed] NCT00411138
=Advanced or metastatic disease, first-line=
+
## '''Update:''' de Boer SM, Powell ME, Mileshkin L, Katsaros D, Bessette P, Haie-Meder C, Ottevanger PB, Ledermann JA, Khaw P, D'Amico R, Fyles A, Baron MH, Jürgenliemk-Schulz IM, Kitchener HC, Nijman HW, Wilson G, Brooks S, Gribaudo S, Provencher D, Hanzen C, Kruitwagen RF, Smit VTHBM, Singh N, Do V, Lissoni A, Nout RA, Feeney A, Verhoeven-Adema KW, Putter H, Creutzberg CL; PORTEC Study Group. Adjuvant chemoradiotherapy versus radiotherapy alone in women with high-risk endometrial cancer (PORTEC-3): patterns of recurrence and post-hoc survival analysis of a randomised phase 3 trial. Lancet Oncol. 2019 Sep;20(9):1273-1285. Epub 2019 Jul 22. Erratum in: Lancet Oncol. 2019 Sep;20(9):e468. [https://doi.org/10.1016/S1470-2045(19)30395-X link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/31345626 PubMed]
==CapeOx & Panitumumab {{#subobject:22cf7b|Regimen=1}}==
+
==Radiation therapy {{#subobject:24a846|Regimen=1}}==
CapeOx & Panitumumab: '''<u>Cape</u>'''citabine, '''<u>Ox</u>'''aliplatin, Panitumumab
+
RT: '''<u>R</u>'''adiation '''<u>T</u>'''herapy
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen {{#subobject:944ac6|Variant=1}}===
+
===Regimen {{#subobject:4bfd6d|Variant=1}}===
{| class="wikitable" style="width: 40%; text-align:center;"  
+
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
! style="width: 25%" |Study
+
!style="width: 20%"|Study
! style="width: 25%" |[[Levels_of_Evidence#Evidence|Evidence]]
+
!style="width: 20%"|Years of enrollment
 +
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 +
!style="width: 20%"|Comparator
 +
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 +
|-
 +
|[https://www.gynecologiconcology-online.net/article/S0090-8258(03)00863-1 Keys et al. 2004 (GOG 99)]
 +
|1987-1995
 +
|style="background-color:#1a9851"|Phase 3 (E-esc)
 +
|[[Endometrial_cancer_-_null_regimens#Observation|Observation]]
 +
| style="background-color:#1a9850" |Superior RFS
 +
|-
 +
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2360651/ Maggi et al. 2006]
 +
|1990-1997
 +
|style="background-color:#1a9851"|Phase 3 (C)
 +
|[[#CAP_99|CAP]]
 +
| style="background-color:#ffffbf" |Did not meet primary endpoints of PFS/OS
 +
|-
 +
|[https://www.gynecologiconcology-online.net/article/S0090-8258(07)00786-X Susumu et al. 2007 (JGOG 2033)]
 +
|1994-2000
 +
|style="background-color:#1a9851"|Phase 3 (C)
 +
|[[#CAP_99|CAP]]
 +
| style="background-color:#ffffbf" |Did not meet primary endpoint of OS60
 +
|-
 +
|[http://www.gynecologiconcology-online.net/article/S0090-8258(08)00938-4 Homesley et al. 2008 (GOG 184)]
 +
|2000-2004
 +
| style="background-color:#91cf61" |Non-randomized portion of RCT
 +
| style="background-color:#d3d3d3" |
 +
| style="background-color:#d3d3d3" |
 
|-
 
|-
|[https://doi.org/10.1007/s12032-018-1160-1 Papaxoinis et al. 2018 (HE 6A/09)]
+
|[https://doi.org/10.1016/S1470-2045(18)30079-2 de Boer et al. 2018 (PORTEC-3)]
| style="background-color:#91cf61" |Phase 2
+
|2006-2013
 +
|style="background-color:#1a9851"|Phase 3 (C)
 +
|[[#Cisplatin_.26_RT|Cisplatin & RT]], then [[#Carboplatin_.26_Paclitaxel_.28CP.29|Carboplatin & Paclitaxel]]
 +
| style="background-color:#fc8d59" |Seems to have inferior OS<sup>1</sup>
 
|-
 
|-
 
|}
 
|}
<div class="toccolours" style="background-color:#fdcdac">
+
''<sup>1</sup>Reported efficacy for PORTEC-3 is based on the 2019 update.''<br>
====Biomarker eligibility criteria====
+
''Note: in PORTEC-3, radiation is to start within 4 to 6 weeks after surgery, and no later than 8 weeks.''
*Wild-type KRAS, Wild-type NRAS
+
<div class="toccolours" style="background-color:#cbd5e8">
 +
====Preceding treatment====
 +
*[[Surgery#Endometrial_cancer_surgery|Surgery]]
 
</div>
 
</div>
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
====Chemotherapy====
+
====Radiotherapy====
*[[Capecitabine (Xeloda)]] 1000 mg/m<sup>2</sup> PO twice per day on days 1 to 14
+
*[[External beam radiotherapy]] to the pelvis, 40 to 50 Gy
*[[Oxaliplatin (Eloxatin)]] 130 mg/m<sup>2</sup> IV once on day 1
+
**If cervical involvement, brachytherapy boost
====Targeted therapy====
+
'''One course'''
*[[Panitumumab (Vectibix)]] 9 mg/kg IV once on day 1
+
</div>
'''21-day cycles'''
+
<div class="toccolours" style="background-color:#cbd5e7">
 +
====Subsequent treatment====
 +
*GOG 184: [[#Cisplatin_.26_Doxorubicin|CD]] x 6 versus [[#CDP_99|CDP]] x 6
 
</div></div>
 
</div></div>
 
===References===
 
===References===
#'''HE 6A/09:''' Papaxoinis G, Kotoula V, Giannoulatou E, Koliou GA, Karavasilis V, Lakis S, Koureas A, Bobos M, Chalaralambous E, Daskalaki E, Chatzopoulos K, Tsironis G, Pazarli E, Chrisafi S, Samantas E, Kaklamanos IG, Varthalitis I, Konstantara A, Syrigos KN, Pentheroudakis G, Pectasides D, Fountzilas G. Phase II study of panitumumab combined with capecitabine and oxaliplatin as first-line treatment in metastatic colorectal cancer patients: clinical results including extended tumor genotyping. Med Oncol. 2018 May 31;35(7):101. [https://doi.org/10.1007/s12032-018-1160-1 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/29855806 PubMed] NCT01215539
+
# '''GOG 99:''' Keys HM, Roberts JA, Brunetto VL, Zaino RJ, Spirtos NM, Bloss JD, Pearlman A, Maiman MA, Bell JG; Gynecologic Oncology Group. A phase III trial of surgery with or without adjunctive external pelvic radiation therapy in intermediate risk endometrial adenocarcinoma: a Gynecologic Oncology Group study. Gynecol Oncol. 2004 Mar;92(3):744-51. Erratum in: Gynecol Oncol. 2004 Jul;94(1):241-2. [https://www.gynecologiconcology-online.net/article/S0090-8258(03)00863-1 link to original article] [https://pubmed.ncbi.nlm.nih.gov/14984936 PubMed]
==FOLFIRI & Bevacizumab {{#subobject:80d6b8|Regimen=1}}==
+
# Maggi R, Lissoni A, Spina F, Melpignano M, Zola P, Favalli G, Colombo A, Fossati R. Adjuvant chemotherapy vs radiotherapy in high-risk endometrial carcinoma: results of a randomised trial. Br J Cancer. 2006 Aug 7;95(3):266-71. Epub 2006 Jul 25. [https://www.nature.com/articles/6603279 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2360651/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/16868539 PubMed]
FOLFIRI & Bevacizumab: '''<u>FOL</u>'''inic acid, '''<u>F</u>'''luorouracil, '''<u>IRI</u>'''notecan, Bevacizumab
+
# '''JGOG 2033:''' Susumu N, Sagae S, Udagawa Y, Niwa K, Kuramoto H, Satoh S, Kudo R; Japanese Gynecologic Oncology Group. Randomized phase III trial of pelvic radiotherapy versus cisplatin-based combined chemotherapy in patients with intermediate- and high-risk endometrial cancer: a Japanese Gynecologic Oncology Group study. Gynecol Oncol. 2008 Jan;108(1):226-33. Epub 2007 Nov 9. [https://www.gynecologiconcology-online.net/article/S0090-8258(07)00786-X link to original article] [https://pubmed.ncbi.nlm.nih.gov/17996926 PubMed]
 +
# '''GOG 184:''' Homesley HD, Filiaci V, Gibbons SK, Long HJ, Cella D, Spirtos NM, Morris RT, DeGeest K, Lee R, Montag A. A randomized phase III trial in advanced endometrial carcinoma of surgery and volume directed radiation followed by cisplatin and doxorubicin with or without paclitaxel: A Gynecologic Oncology Group study. Gynecol Oncol. 2009 Mar;112(3):543-52. Epub 2008 Dec 23. [http://www.gynecologiconcology-online.net/article/S0090-8258(08)00938-4 link to original article] '''contains dosing details in manuscript''' [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4459781/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/19108877 PubMed] NCT00006011
 +
## '''Update:''' Spirtos NM, Enserro D, Homesley HD, Gibbons SK, Cella D, Morris RT, DeGeest K, Lee RB, Miller DS. The addition of paclitaxel to doxorubicin and cisplatin and volume-directed radiation does not improve overall survival (OS) or long-term recurrence-free survival (RFS) in advanced endometrial cancer (EC): a randomized phase III NRG/Gynecologic Oncology Group (GOG) study. Gynecol Oncol. 2019 Jul;154(1):13-21. Epub 2019 Apr 30. [https://doi.org/10.1016/j.ygyno.2019.03.240 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6852648/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/31053405 PubMed]
 +
# '''PORTEC-3:''' de Boer SM, Powell ME, Mileshkin L, Katsaros D, Bessette P, Haie-Meder C, Ottevanger PB, Ledermann JA, Khaw P, Colombo A, Fyles A, Baron MH, Jürgenliemk-Schulz IM, Kitchener HC, Nijman HW, Wilson G, Brooks S, Carinelli S, Provencher D, Hanzen C, Lutgens LCHW, Smit VTHBM, Singh N, Do V, D'Amico R, Nout RA, Feeney A, Verhoeven-Adema KW, Putter H, Creutzberg CL; PORTEC study group. Adjuvant chemoradiotherapy versus radiotherapy alone for women with high-risk endometrial cancer (PORTEC-3): final results of an international, open-label, multicentre, randomised, phase 3 trial. Lancet Oncol. 2018 Mar;19(3):295-309. Epub 2018 Feb 12. [https://doi.org/10.1016/S1470-2045(18)30079-2 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5840256/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/29449189 PubMed] NCT00411138
 +
## '''Update:''' de Boer SM, Powell ME, Mileshkin L, Katsaros D, Bessette P, Haie-Meder C, Ottevanger PB, Ledermann JA, Khaw P, D'Amico R, Fyles A, Baron MH, Jürgenliemk-Schulz IM, Kitchener HC, Nijman HW, Wilson G, Brooks S, Gribaudo S, Provencher D, Hanzen C, Kruitwagen RF, Smit VTHBM, Singh N, Do V, Lissoni A, Nout RA, Feeney A, Verhoeven-Adema KW, Putter H, Creutzberg CL; PORTEC Study Group. Adjuvant chemoradiotherapy versus radiotherapy alone in women with high-risk endometrial cancer (PORTEC-3): patterns of recurrence and post-hoc survival analysis of a randomised phase 3 trial. Lancet Oncol. 2019 Sep;20(9):1273-1285. Epub 2019 Jul 22. Erratum in: Lancet Oncol. 2019 Sep;20(9):e468. [https://doi.org/10.1016/S1470-2045(19)30395-X link to original article] [https://pubmed.ncbi.nlm.nih.gov/31345626 PubMed]
 +
==Whole abdominal radiation (WAI) {{#subobject:37c051|Regimen=1}}==
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen {{#subobject:28b67a|Variant=1}}===
+
===Regimen {{#subobject:1ab715|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
Line 271: Line 322:
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
|-
 
|-
|[https://doi.org/10.1016/S1470-2045(14)70330-4 Heinemann et al. 2014 (FIRE-3)]
+
|[https://doi.org/10.1200/jco.2004.00.7617 Randall et al. 2006 (GOG 122)]
|2007-2012 (C)
+
|1992-2000
| style="background-color:#1a9851" |Phase 3 (E-switch-ic)
+
|style="background-color:#1a9851"|Phase 3 (E-switch-ooc)
|[[#FOLFIRI_.26_Cetuximab_2|FOLFIRI & Cetuximab]]
+
|[[#Cisplatin_.26_Doxorubicin|Cisplatin & Doxorubicin]]
| style="background-color:#ffffbf" |Did not meet primary endpoint of ORR
+
|style="background-color:#d73027"|Inferior OS
 +
|-
 +
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2752331 Wolfson et al. 2007 (GOG 150)]
 +
|1993-2005
 +
|style="background-color:#1a9851"|Phase 3 (C)
 +
|[[#CIM|CIM]]
 +
|style="background-color:#fee08b"|Might have inferior OS
 +
|-
 +
|}
 +
''Not commonly used but was a comparator arm; here for reference purposes only.''
 +
====Radiotherapy====
 +
*[[External beam radiotherapy]]
 +
</div></div>
 +
===References===
 +
# '''GOG 122:''' Randall ME, Filiaci VL, Muss H, Spirtos NM, Mannel RS, Fowler J, Thigpen JT, Benda JA; Gynecologic Oncology Group. Randomized phase III trial of whole-abdominal irradiation versus doxorubicin and cisplatin chemotherapy in advanced endometrial carcinoma: a Gynecologic Oncology Group study. J Clin Oncol. 2006 Jan 1;24(1):36-44. Epub 2005 Dec 5. [https://doi.org/10.1200/jco.2004.00.7617 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/16330675 PubMed]
 +
# '''GOG 150:''' Wolfson AH, Brady MF, Rocereto T, Mannel RS, Lee YC, Futoran RJ, Cohn DE, Ioffe OB. A Gynecologic Oncology Group randomized phase III trial of whole abdominal irradiation (WAI) vs cisplatin-ifosfamide and mesna (CIM) as post-surgical therapy in stage I-IV carcinosarcoma (CS) of the uterus. Gynecol Oncol. 2007 Nov;107(2):177-85. Epub 2007 Sep 5. [https://www.gynecologiconcology-online.net/article/S0090-8258(07)00567-7 link to original article] '''contains dosing details in manuscript''' [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2752331/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/17822748 PubMed] NCT00002546
 +
=Non-endocrine therapy for advanced, recurrent, or metastatic disease=
 +
==Bevacizumab monotherapy {{#subobject:b29ce2|Regimen=1}}==
 +
<div class="toccolours" style="background-color:#eeeeee">
 +
===Regimen {{#subobject:8159f4|Variant=1}}===
 +
{| class="wikitable" style="width: 40%; text-align:center;"
 +
!style="width: 25%"|Study
 +
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 +
|-
 +
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3107744/ Aghajanian et al. 2011 (GOG-0229E)]
 +
|style="background-color:#91cf61"|Phase 2
 
|-
 
|-
 
|}
 
|}
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
====Chemotherapy====
 
*[[Folinic acid (Leucovorin)]] 400 mg/m<sup>2</sup> IV over 2 hours once on day 1, '''given first, with irinotecan'''
 
*[[Fluorouracil (5-FU)]] 400 mg/m<sup>2</sup> IV bolus once on day 1, then 2400 mg/m<sup>2</sup> IV continuous infusion over 46 to 48 hours, '''given third''' (total dose per cycle: 2800 mg/m<sup>2</sup>)
 
*[[Irinotecan (Camptosar)]] 180 mg/m<sup>2</sup> IV over 30 to 90 minutes once on day 1, '''given first, with leucovorin'''
 
 
====Targeted therapy====
 
====Targeted therapy====
*[[Bevacizumab (Avastin)]] 5 mg/kg IV once on day 1, '''given second'''
+
*[[Bevacizumab (Avastin)]] 15 mg/kg IV once on day 1
**In FIRE-3, initial infusion is over 90 minutes, next over 60 minutes, and subsequently over 30 minutes
+
'''21-day cycles'''
'''14-day cycles'''
 
 
</div></div>
 
</div></div>
 
===References===
 
===References===
#'''FIRE-3:''' Heinemann V, von Weikersthal LF, Decker T, Kiani A, Vehling-Kaiser U, Al-Batran SE, Heintges T, Lerchenmüller C, Kahl C, Seipelt G, Kullmann F, Stauch M, Scheithauer W, Hielscher J, Scholz M, Müller S, Link H, Niederle N, Rost A, Höffkes HG, Moehler M, Lindig RU, Modest DP, Rossius L, Kirchner T, Jung A, Stintzing S. FOLFIRI plus cetuximab versus FOLFIRI plus bevacizumab as first-line treatment for patients with metastatic colorectal cancer (FIRE-3): a randomised, open-label, phase 3 trial. Lancet Oncol. 2014 Sep;15(10):1065-75. Epub 2014 Jul 31.[https://doi.org/10.1016/S1470-2045(14)70330-4 link to original article] [https://pubmed.ncbi.nlm.nih.gov/25088940 PubMed] NCT00433927
+
<!-- Presented in part at the 45th Annual Meeting of the American Society of Clinical Oncology, May 29-June 2, 2009, Orlando, FL. -->
==FOLFIRI & Cetuximab {{#subobject:11cf7b|Regimen=1}}==
+
# '''GOG-0229E:''' Aghajanian C, Sill MW, Darcy KM, Greer B, McMeekin DS, Rose PG, Rotmensch J, Barnes MN, Hanjani P, Leslie KK; Gynecologic Oncology Group. Phase II trial of bevacizumab in recurrent or persistent endometrial cancer: a Gynecologic Oncology Group study. J Clin Oncol. 2011 Jun 1;29(16):2259-65. Epub 2011 May 2. [https://doi.org/10.1200/jco.2010.32.6397 link to original article] '''contains dosing details in manuscript''' [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3107744/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/21537039 PubMed] NCT00301964
FOLFIRI & Cetuximab: '''<u>FOL</u>'''inic acid, '''<u>F</u>'''luorouracil, '''<u>IRI</u>'''notecan, Cetuximab
+
==Carboplatin monotherapy {{#subobject:f9b8ad|Regimen=1}}==
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen {{#subobject:921ac6|Variant=1}}===
+
===Regimen variant #1, 300 mg/m<sup>2</sup> {{#subobject:6a2df1|Variant=1}}===
{| class="wikitable" style="color:white; background-color:#404040"
+
{| class="wikitable" style="width: 60%; text-align:center;"
|<small>'''FDA-recommended dose'''</small>
+
!style="width: 33%"|Study
 +
!style="width: 33%"|[[Levels_of_Evidence#Evidence|Evidence]]
 +
!style="width: 33%"|[[Levels_of_Evidence#Efficacy|Efficacy]]
 +
|-
 +
|[https://www.ejcancer.com/article/S0959-8049(02)00504-X van Wijk et al. 2003]
 +
|style="background-color:#91cf61"|Phase 2
 +
| style="background-color:#88419d; color:white |ORR: 13% (95% CI 6-25%)
 
|-
 
|-
 
|}
 
|}
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
+
''This dosing is intended for patients previously treated with chemotherapy.''
!style="width: 20%"|Study
+
====Chemotherapy====
!style="width: 20%"|Years of enrollment
+
*[[Carboplatin (Paraplatin)]] 300 mg/m<sup>2</sup> IV over 30 minutes once on day 1
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
+
'''28-day cycles'''
!style="width: 20%"|Comparator
+
</div></div><br>
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
+
<div class="toccolours" style="background-color:#eeeeee">
|-
+
===Regimen variant #2, 400 mg/m<sup>2</sup> {{#subobject:2d401b|Variant=1}}===
|[https://doi.org/10.1056/NEJMoa0805019 Van Cutsem et al. 2009 (CRYSTAL)]
+
{| class="wikitable" style="width: 60%; text-align:center;"  
|2004-2005 (C)
+
!style="width: 33%"|Study
| style="background-color:#1a9851" |Phase 3 (E-RT-esc)
+
!style="width: 33%"|[[Levels_of_Evidence#Evidence|Evidence]]
|[[#FOLFIRI|FOLFIRI]]
+
!style="width: 33%"|[[Levels_of_Evidence#Efficacy|Efficacy]]
| style="background-color:#1a9850" |Superior OS<sup>1</sup><br>Median OS: 23.5 vs 19.5 mo<br>(HR 0.81, 95% CI 0.69-0.94)
 
 
|-
 
|-
|[https://doi.org/10.1016/S1470-2045(14)70330-4 Heinemann et al. 2014 (FIRE-3)]
+
|[https://www.ejcancer.com/article/S0959-8049(02)00504-X van Wijk et al. 2003]
|2007-2012 (C)
+
|style="background-color:#91cf61"|Phase 2
| style="background-color:#1a9851" |Phase 3 (E-switch-ooc)
+
| style="background-color:#88419d; color:white |ORR: 13% (95% CI 6-25%)
|[[#FOLFIRI_.26_Bevacizumab|FOLFIRI & Bevacizumab]]
 
| style="background-color:#ffffbf" |Did not meet primary endpoint of ORR
 
 
|-
 
|-
 
|}
 
|}
''<sup>1</sup>Reported efficacy for CRYSTAL is based on the 2012 pooled update and is only for KRAS wild-type tumors.''
 
<div class="toccolours" style="background-color:#fdcdac">
 
====Biomarker eligibility criteria====
 
*CRYSTAL: none
 
*FIRE-3: Wild-type KRAS, Wild-type NRAS
 
</div>
 
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
*[[Folinic acid (Leucovorin)]] 400 mg/m<sup>2</sup> IV over 2 hours once on day 1, '''given second, 1 hour after completion of cetuximab, with irinotecan'''
+
*[[Carboplatin (Paraplatin)]] 400 mg/m<sup>2</sup> IV over 30 minutes once on day 1
*[[Fluorouracil (5-FU)]] 400 mg/m<sup>2</sup> IV bolus once on day 1, then 2400 mg/m<sup>2</sup> IV continuous infusion over 46 hours, '''given third''' (total dose per cycle: 2800 mg/m<sup>2</sup>)
+
'''28-day cycles'''
*[[Irinotecan (Camptosar)]] 180 mg/m<sup>2</sup> IV over 30 to 90 minutes once on day 1, '''given second, 1 hour after completion of cetuximab, with leucovorin'''
 
====Targeted therapy====
 
*[[Cetuximab (Erbitux)]] as follows, '''given first and completed at least 1 hour before FOLFIRI begins''':
 
**Cycle 1: 400 mg/m<sup>2</sup> IV over 2 hours once on day 1, then 250 mg/m<sup>2</sup> IV over 60 minutes once on day 8
 
**Cycle 2 onwards: 250 mg/m<sup>2</sup> IV over 60 minutes once per day on days 1 & 8
 
'''14-day cycles'''
 
 
</div></div>
 
</div></div>
 
===References===
 
===References===
#'''CRYSTAL:''' Van Cutsem E, Köhne CH, Hitre E, Zaluski J, Chang Chien CR, Makhson A, D'Haens G, Pintér T, Lim R, Bodoky G, Roh JK, Folprecht G, Ruff P, Stroh C, Tejpar S, Schlichting M, Nippgen J, Rougier P. Cetuximab and chemotherapy as initial treatment for metastatic colorectal cancer. N Engl J Med. 2009 Apr 2;360(14):1408-17. [https://doi.org/10.1056/NEJMoa0805019 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/19339720 PubMed] NCT00154102
+
# van Wijk FH, Lhommé C, Bolis G, Scotto di Palumbo V, Tumolo S, Nooij M, Freire de Oliveira C, Vermorken JB; [[Study_Groups#EORTC|EORTC]] Gynaecological Cancer Group. Phase II study of carboplatin in patients with advanced or recurrent endometrial carcinoma: a trial of the EORTC Gynaecological Cancer Group. Eur J Cancer. 2003 Jan;39(1):78-85. [https://www.ejcancer.com/article/S0959-8049(02)00504-X link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/12504662 PubMed]
<!-- ## '''Update: Abstract:''' E. Van Cutsem, I. Lang, G. Folprecht, M. Nowacki, C. Barone, I. Shchepotin, J. Maurel, D. Cunningham, I. Celik, C. Kohne. Cetuximab plus FOLFIRI: Final data from the CRYSTAL study on the association of KRAS and BRAF biomarker status with treatment outcome. 2010 ASCO Annual Meeting abstract 3570. [http://www.asco.org/ascov2/Meetings/Abstracts?&vmview=abst_detail_view&confID=74&abstractID=54429 link to abstract] -->
+
==Carboplatin & Paclitaxel (CP) {{#subobject:b0e21f|Regimen=1}}==
##'''Update:''' Van Cutsem E, Köhne CH, Láng I, Folprecht G, Nowacki MP, Cascinu S, Shchepotin I, Maurel J, Cunningham D, Tejpar S, Schlichting M, Zubel A, Celik I, Rougier P, Ciardiello F. Cetuximab plus irinotecan, fluorouracil, and leucovorin as first-line treatment for metastatic colorectal cancer: updated analysis of overall survival according to tumor KRAS and BRAF mutation status. J Clin Oncol. 2011 May 20;29(15):2011-9. Epub 2011 Apr 18. [https://doi.org/10.1200/jco.2010.33.5091 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/21502544 PubMed]
 
##'''Pooled update:''' Bokemeyer C, Van Cutsem E, Rougier P, Ciardiello F, Heeger S, Schlichting M, Celik I, Köhne CH. Addition of cetuximab to chemotherapy as first-line treatment for KRAS wild-type metastatic colorectal cancer: Pooled analysis of the CRYSTAL and OPUS randomised clinical trials. Eur J Cancer. 2012 Jul;48(10):1466-75. Epub 2012 Mar 23. [https://www.ejcancer.com/article/S0959-8049(12)00209-2 link to original article] [https://pubmed.ncbi.nlm.nih.gov/22446022 PubMed]
 
##'''Biomarker analysis:''' Van Cutsem E, Lenz HJ, Köhne CH, Heinemann V, Tejpar S, Melezínek I, Beier F, Stroh C, Rougier P, van Krieken JH, Ciardiello F. Fluorouracil, leucovorin, and irinotecan plus cetuximab treatment and RAS mutations in colorectal cancer. J Clin Oncol. 2015 Mar 1;33(7):692-700. Epub 2015 Jan 20. [https://doi.org/10.1200/JCO.2014.59.4812 link to original article] [https://pubmed.ncbi.nlm.nih.gov/25605843 PubMed]
 
#'''FIRE-3:''' Heinemann V, von Weikersthal LF, Decker T, Kiani A, Vehling-Kaiser U, Al-Batran SE, Heintges T, Lerchenmüller C, Kahl C, Seipelt G, Kullmann F, Stauch M, Scheithauer W, Hielscher J, Scholz M, Müller S, Link H, Niederle N, Rost A, Höffkes HG, Moehler M, Lindig RU, Modest DP, Rossius L, Kirchner T, Jung A, Stintzing S. FOLFIRI plus cetuximab versus FOLFIRI plus bevacizumab as first-line treatment for patients with metastatic colorectal cancer (FIRE-3): a randomised, open-label, phase 3 trial. Lancet Oncol. 2014 Sep;15(10):1065-75. Epub 2014 Jul 31. [https://doi.org/10.1016/S1470-2045(14)70330-4 link to original article] [https://pubmed.ncbi.nlm.nih.gov/25088940 PubMed] NCT00433927
 
==FOLFIRI & Cetuximab (L-Leucovorin) {{#subobject:22bf7b|Regimen=1}}==
 
FOLFIRI & Cetuximab: L-'''<u>FOL</u>'''inic acid, '''<u>F</u>'''luorouracil, '''<u>IRI</u>'''notecan, Cetuximab
 
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen {{#subobject:8ugac6|Variant=1}}===
+
===Regimen variant #1, 5/175, finite duration {{#subobject:7ab5c0|Variant=1}}===
{| class="wikitable" style="color:white; background-color:#404040"
+
{| class="wikitable" style="width: 40%; text-align:center;"
|<small>'''FDA-recommended dose'''</small>
+
!style="width: 25%"|Study
 +
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 +
|-
 +
|[http://www.gynecologiconcology-online.net/article/S0090-8258(08)00083-8 Pectasides et al. 2008]
 +
|style="background-color:#91cf61"|Phase 2
 +
|-
 +
|}
 +
<div class="toccolours" style="background-color:#b3e2cd">
 +
====Chemotherapy====
 +
*[[Carboplatin (Paraplatin)]] AUC 5 IV over 60 minutes once on day 1, '''given second'''
 +
*[[Paclitaxel (Taxol)]] 175 mg/m<sup>2</sup> IV over 3 hours once on day 1, '''given first'''
 +
'''21-day cycle for 6 to 9 cycles'''
 +
</div></div><br>
 +
<div class="toccolours" style="background-color:#eeeeee">
 +
===Regimen variant #2, 5/175, indefinite {{#subobject:100919|Variant=1}}===
 +
{| class="wikitable" style="width: 40%; text-align:center;"
 +
!style="width: 25%"|Study
 +
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 +
|-
 +
|[https://doi.org/10.1200/jco.2001.19.20.4048 Hoskins et al. 2001]
 +
|style="background-color:#91cf61"|Phase 2
 +
|-
 +
|[https://ijgc.bmj.com/content/18/4/803.abstract Sorbe et al. 2007]
 +
|style="background-color:#91cf61"|Phase 2
 +
|-
 +
|}
 +
''Note: this is the lower limit of carboplatin dosing allowed in Hoskins et al. 2001.''
 +
<div class="toccolours" style="background-color:#b3e2cd">
 +
====Chemotherapy====
 +
*[[Carboplatin (Paraplatin)]] AUC 5 IV over 60 minutes once on day 1, '''given second'''
 +
*[[Paclitaxel (Taxol)]] 175 mg/m<sup>2</sup> IV over 3 hours once on day 1, '''given first'''
 +
'''21-day cycles'''
 +
</div></div><br>
 +
<div class="toccolours" style="background-color:#eeeeee">
 +
===Regimen variant #3, 6/175 x 7 {{#subobject:a3c4b2|Variant=1}}===
 +
{| class="wikitable" style="color:black; background-color:#42f584"
 +
|<small>'''ESMO-preferred (I-A, 2016)'''</small>
 
|-
 
|-
 
|}
 
|}
Line 357: Line 449:
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
|-
 
|-
|[https://doi.org/10.1056/NEJMoa0805019 Van Cutsem et al. 2009 (CRYSTAL)]
+
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7676887/ Miller et al. 2020 (GOG0209)]
|2004-2005 (C)
+
|2003-2009
| style="background-color:#1a9851" |Phase 3 (E-RT-esc)
+
| style="background-color:#1a9851" |Phase 3 (E-de-esc)
|[[#FOLFIRI|FOLFIRI]]
+
|[[#Cisplatin.2C_Doxorubicin.2C_Paclitaxel|TAP]]
| style="background-color:#1a9850" |Superior OS<sup>1</sup><br>Median OS: 23.5 vs 19.5 mo<br>(HR 0.81, 95% CI 0.69-0.94)
+
| style="background-color:#eeee01" |Non-inferior OS<br>Median OS: 37 vs 41 mo<br>(HR 1.002, 90% CI 0.9-1.12)
|-
 
|[https://doi.org/10.1016/S1470-2045(14)70330-4 Heinemann et al. 2014 (FIRE-3)]
 
|2007-2012 (C)
 
| style="background-color:#1a9851" |Phase 3 (E-switch-ooc)
 
|[[#FOLFIRI_.26_Bevacizumab|FOLFIRI & Bevacizumab]]
 
| style="background-color:#ffffbf" |Did not meet primary endpoint of ORR
 
 
|-
 
|-
 
|}
 
|}
''<sup>1</sup>Reported efficacy for CRYSTAL is based on the 2012 pooled update and is only for KRAS wild-type tumors.''
+
''Note: ESMO recommends 6 cycles, whereas the cited RCT uses 7 cycles.''
<div class="toccolours" style="background-color:#fdcdac">
 
====Biomarker eligibility criteria====
 
*CRYSTAL: none
 
*FIRE-3: Wild-type KRAS, Wild-type NRAS
 
</div>
 
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
*[[Levoleucovorin (Fusilev)]] 200 mg/m<sup>2</sup> IV over 2 hours once on day 1, '''given second, 1 hour after completion of cetuximab, with irinotecan'''
+
*[[Carboplatin (Paraplatin)]] AUC 6 IV once on day 1, '''given second'''
*[[Fluorouracil (5-FU)]] 400 mg/m<sup>2</sup> IV bolus once on day 1, then 2400 mg/m<sup>2</sup> IV continuous infusion over 46 hours, '''given third''' (total dose per cycle: 2800 mg/m<sup>2</sup>)
+
*[[Paclitaxel (Taxol)]] 175 mg/m<sup>2</sup> IV over 3 hours once on day 1, '''given first'''
*[[Irinotecan (Camptosar)]] 180 mg/m<sup>2</sup> IV over 30 to 90 minutes once on day 1, '''given second, 1 hour after completion of cetuximab, with L-leucovorin'''
+
'''21-day cycle for 7 cycles'''
====Targeted therapy====
+
</div></div><br>
*[[Cetuximab (Erbitux)]] as follows, '''given first and completed at least 1 hour before FOLFIRI begins''':
 
**Cycle 1: 400 mg/m<sup>2</sup> IV over 2 hours once on day 1, then 250 mg/m<sup>2</sup> IV over 60 minutes once on day 8
 
**Cycle 2 onwards: 250 mg/m<sup>2</sup> IV over 60 minutes once per day on days 1 & 8
 
'''14-day cycles'''
 
</div></div>
 
===References===
 
#'''CRYSTAL:''' Van Cutsem E, Köhne CH, Hitre E, Zaluski J, Chang Chien CR, Makhson A, D'Haens G, Pintér T, Lim R, Bodoky G, Roh JK, Folprecht G, Ruff P, Stroh C, Tejpar S, Schlichting M, Nippgen J, Rougier P. Cetuximab and chemotherapy as initial treatment for metastatic colorectal cancer. N Engl J Med. 2009 Apr 2;360(14):1408-17. [https://doi.org/10.1056/NEJMoa0805019 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/19339720 PubMed] NCT00154102
 
<!-- ## '''Update: Abstract:''' E. Van Cutsem, I. Lang, G. Folprecht, M. Nowacki, C. Barone, I. Shchepotin, J. Maurel, D. Cunningham, I. Celik, C. Kohne. Cetuximab plus FOLFIRI: Final data from the CRYSTAL study on the association of KRAS and BRAF biomarker status with treatment outcome. 2010 ASCO Annual Meeting abstract 3570. [http://www.asco.org/ascov2/Meetings/Abstracts?&vmview=abst_detail_view&confID=74&abstractID=54429 link to abstract] -->
 
##'''Update:''' Van Cutsem E, Köhne CH, Láng I, Folprecht G, Nowacki MP, Cascinu S, Shchepotin I, Maurel J, Cunningham D, Tejpar S, Schlichting M, Zubel A, Celik I, Rougier P, Ciardiello F. Cetuximab plus irinotecan, fluorouracil, and leucovorin as first-line treatment for metastatic colorectal cancer: updated analysis of overall survival according to tumor KRAS and BRAF mutation status. J Clin Oncol. 2011 May 20;29(15):2011-9. Epub 2011 Apr 18. [https://doi.org/10.1200/jco.2010.33.5091 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/21502544 PubMed]
 
##'''Pooled update:''' Bokemeyer C, Van Cutsem E, Rougier P, Ciardiello F, Heeger S, Schlichting M, Celik I, Köhne CH. Addition of cetuximab to chemotherapy as first-line treatment for KRAS wild-type metastatic colorectal cancer: Pooled analysis of the CRYSTAL and OPUS randomised clinical trials. Eur J Cancer. 2012 Jul;48(10):1466-75. Epub 2012 Mar 23. [https://www.ejcancer.com/article/S0959-8049(12)00209-2 link to original article] [https://pubmed.ncbi.nlm.nih.gov/22446022 PubMed]
 
##'''Biomarker analysis:''' Van Cutsem E, Lenz HJ, Köhne CH, Heinemann V, Tejpar S, Melezínek I, Beier F, Stroh C, Rougier P, van Krieken JH, Ciardiello F. Fluorouracil, leucovorin, and irinotecan plus cetuximab treatment and RAS mutations in colorectal cancer. J Clin Oncol. 2015 Mar 1;33(7):692-700. Epub 2015 Jan 20. [https://doi.org/10.1200/JCO.2014.59.4812 link to original article] [https://pubmed.ncbi.nlm.nih.gov/25605843 PubMed]
 
#'''FIRE-3:''' Heinemann V, von Weikersthal LF, Decker T, Kiani A, Vehling-Kaiser U, Al-Batran SE, Heintges T, Lerchenmüller C, Kahl C, Seipelt G, Kullmann F, Stauch M, Scheithauer W, Hielscher J, Scholz M, Müller S, Link H, Niederle N, Rost A, Höffkes HG, Moehler M, Lindig RU, Modest DP, Rossius L, Kirchner T, Jung A, Stintzing S. FOLFIRI plus cetuximab versus FOLFIRI plus bevacizumab as first-line treatment for patients with metastatic colorectal cancer (FIRE-3): a randomised, open-label, phase 3 trial. Lancet Oncol. 2014 Sep;15(10):1065-75. Epub 2014 Jul 31. [https://doi.org/10.1016/S1470-2045(14)70330-4 link to original article] [https://pubmed.ncbi.nlm.nih.gov/25088940 PubMed] NCT00433927
 
==FOLFOX4 {{#subobject:7239a0|Regimen=1}}==
 
FOLFOX4: '''<u>FOL</u>'''inic acid, '''<u>F</u>'''luorouracil, '''<u>OX</u>'''aliplatin
 
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen {{#subobject:ab483a|Variant=1}}===
+
===Regimen variant #4, 6/175 x 6-10 {{#subobject:a3jqb2|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
Line 405: Line 472:
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
|-
 
|-
|[https://doi.org/10.1200/JCO.2008.20.8397 Bokemeyer et al. 2008 (OPUS)]
+
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8937015/ Powell et al. 2022 (GOG-0261)]
|2005-2006
+
|2009-2014
| style="background-color:#1a9851" |Randomized Phase 2 (C)
+
| style="background-color:#1a9851" |Phase 3 (E-switch-ic)
|[[#FOLFOX4_.26_Cetuximab|FOLFOX4 & Cetuximab]]
+
|[[#Ifosfamide_.26_Paclitaxel|Ifosfamide & Paclitaxel]]
| style="background-color:#d73027" |Inferior OS<sup>1</sup>
+
| style="background-color:#eeee01" |Non-inferior OS<br>Median OS: 37 vs 29 mo<br>(HR 0.87, 90% CI 0.70-1.075)
 
|-
 
|-
|[https://doi.org/10.1200/jco.2009.27.4860 Douillard et al. 2010 (PRIME)]
+
|}
|2006-2008 (C)
+
<div class="toccolours" style="background-color:#b3e2cd">
| style="background-color:#1a9851" |Phase 3 (C)
+
====Chemotherapy====
|[[#FOLFOX4_.26_Panitumumab|FOLFOX4 & Panitumumab]]
+
*[[Carboplatin (Paraplatin)]] AUC 6 IV once on day 1, '''given second'''
| style="background-color:#fc8d59" |Seems to have inferior PFS<sup>2</sup>
+
*[[Paclitaxel (Taxol)]] 175 mg/m<sup>2</sup> IV over 3 hours once on day 1, '''given first'''
 +
'''21-day cycle for 6 to 10 cycles'''
 +
</div></div><br>
 +
<div class="toccolours" style="background-color:#eeeeee">
 +
===Regimen variant #5, 7/175 {{#subobject:3a58ce|Variant=1}}===
 +
{| class="wikitable" style="width: 40%; text-align:center;"
 +
!style="width: 25%"|Study
 +
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
|-
 
|-
|[https://doi.org/10.1200/JCO.2018.78.3183 Qin et al. 2018 (TAILOR-CRC)]
+
|[https://doi.org/10.1200/jco.2001.19.20.4048 Hoskins et al. 2001]
|2010-NR
+
|style="background-color:#91cf61"|Phase 2
| style="background-color:#1a9851" |Phase 3 (C)
 
|[[#FOLFOX4_.26_Cetuximab|FOLFOX4 & Cetuximab]]
 
| style="background-color:#fc8d59" |Seems to have inferior OS
 
 
|-
 
|-
 
|}
 
|}
''<sup>1</sup>Reported efficacy for OPUS is based on the 2012 pooled update and is only for KRAS wild-type tumors.''<br>
+
''Note: this is the upper limit of carboplatin dosing allowed in Hoskins et al. 2001.''
''<sup>2</sup>In PRIME, patients with KRAS wild-type tumors receiving this regimen seem to have inferior OS, based on the 2014 update. Conversely, in KRAS mutants, this regimen seems to have superior PFS.''<br>
 
''Note: TAILOR required RAS wild-type (not just KRAS). Note that there is another trial named TAILOR in non-small cell lung cancer, so this one has been dubbed TAILOR-CRC.''
 
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
*[[Folinic acid (Leucovorin)]] 200 mg/m<sup>2</sup> IV over 2 hours once per day on days 1 & 2, '''given first, with oxaliplatin on day 1'''
+
*[[Carboplatin (Paraplatin)]] AUC 7 IV once on day 1, '''given second'''
*[[Fluorouracil (5-FU)]] 400 mg/m<sup>2</sup> IV bolus once per day on days 1 & 2, then 600 mg/m<sup>2</sup> IV continuous infusion over 22 hours after each bolus, '''given second''' (total dose per cycle: 2000 mg/m<sup>2</sup>)
+
*[[Paclitaxel (Taxol)]] 175 mg/m<sup>2</sup> IV over 3 hours once on day 1, '''given first'''
*[[Oxaliplatin (Eloxatin)]] 85 mg/m<sup>2</sup> IV over 2 hours once on day 1, '''given first'''
+
'''21-day cycles'''
'''14-day cycles'''
 
 
</div></div>
 
</div></div>
 
===References===
 
===References===
#'''OPUS:''' Bokemeyer C, Bondarenko I, Makhson A, Hartmann JT, Aparicio J, de Braud F, Donea S, Ludwig H, Schuch G, Stroh C, Loos AH, Zubel A, Koralewski P. Fluorouracil, leucovorin, and oxaliplatin with and without cetuximab in the first-line treatment of metastatic colorectal cancer. J Clin Oncol. 2009 Feb 10;27(5):663-71. Epub 2008 Dec 29. [https://doi.org/10.1200/JCO.2008.20.8397 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/19114683 PubMed] NCT00125034
+
# Hoskins PJ, Swenerton KD, Pike JA, Wong F, Lim P, Acquino-Parsons C, Lee N. Paclitaxel and carboplatin, alone or with irradiation, in advanced or recurrent endometrial cancer: a phase II study. J Clin Oncol. 2001 Oct 15;19(20):4048-53. [https://doi.org/10.1200/jco.2001.19.20.4048 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/11600606 PubMed]
##'''Update:''' Bokemeyer C, Bondarenko I, Hartmann JT, de Braud F, Schuch G, Zubel A, Celik I, Schlichting M, Koralewski P. Efficacy according to biomarker status of cetuximab plus FOLFOX-4 as first-line treatment for metastatic colorectal cancer: the OPUS study. Ann Oncol. 2011 Jul;22(7):1535-46. Epub 2011 Jan 12. [https://doi.org/10.1093/annonc/mdq632 link to original article] [https://pubmed.ncbi.nlm.nih.gov/21228335 PubMed]
+
# Sorbe B, Andersson H, Boman K, Rosenberg P, Kalling M. Treatment of primary advanced and recurrent endometrial carcinoma with a combination of carboplatin and paclitaxel-long-term follow-up. Int J Gynecol Cancer. 2008 Jul-Aug;18(4):803-8. Epub 2007 Oct 18. [https://ijgc.bmj.com/content/18/4/803.abstract link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/17944917 PubMed]
##'''Pooled update:''' Bokemeyer C, Van Cutsem E, Rougier P, Ciardiello F, Heeger S, Schlichting M, Celik I, Köhne CH. Addition of cetuximab to chemotherapy as first-line treatment for KRAS wild-type metastatic colorectal cancer: Pooled analysis of the CRYSTAL and OPUS randomised clinical trials. Eur J Cancer. 2012 Jul;48(10):1466-75. Epub 2012 Mar 23. [https://www.ejcancer.com/article/S0959-8049(12)00209-2 link to original article] [https://pubmed.ncbi.nlm.nih.gov/22446022 PubMed]
+
# Pectasides D, Xiros N, Papaxoinis G, Pectasides E, Sykiotis C, Koumarianou A, Psyrri A, Gaglia A, Kassanos D, Gouveris P, Panayiotidis J, Fountzilas G, Economopoulos T. Carboplatin and paclitaxel in advanced or metastatic endometrial cancer. Gynecol Oncol. 2008 May;109(2):250-4. Epub 2008 Mar 4. [http://www.gynecologiconcology-online.net/article/S0090-8258(08)00083-8 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/18299146 PubMed] content property of [http://hemonc.org HemOnc.org]
#'''PRIME:''' Douillard JY, Siena S, Cassidy J, Tabernero J, Burkes R, Barugel M, Humblet Y, Bodoky G, Cunningham D, Jassem J, Rivera F, Kocákova I, Ruff P, Błasińska-Morawiec M, Šmakal M, Canon JL, Rother M, Oliner KS, Wolf M, Gansert J. Randomized, phase III trial of panitumumab with infusional fluorouracil, leucovorin, and oxaliplatin (FOLFOX4) versus FOLFOX4 alone as first-line treatment in patients with previously untreated metastatic colorectal cancer: the PRIME study. J Clin Oncol. 2010 Nov 1;28(31):4697-705. Epub 2010 Oct 4. [https://doi.org/10.1200/jco.2009.27.4860 link to original article] [https://pubmed.ncbi.nlm.nih.gov/20921465 PubMed] NCT00364013
+
# '''Retrospective:''' Shechter-Maor G, Bruchim I, Ben-Harim Z, Altaras M, Fishman A. Combined chemotherapy regimen of carboplatin and paclitaxel as adjuvant treatment for papillary serous and clear cell endometrial cancer. Int J Gynecol Cancer. 2009 May;19(4):662-4. [https://ijgc.bmj.com/content/19/4/662-664.abstract link to original article] [https://pubmed.ncbi.nlm.nih.gov/19509567 PubMed]
##'''Biomarker analysis:''' Douillard JY, Oliner KS, Siena S, Tabernero J, Burkes R, Barugel M, Humblet Y, Bodoky G, Cunningham D, Jassem J, Rivera F, Kocákova I, Ruff P, Błasińska-Morawiec M, Šmakal M, Canon JL, Rother M, Williams R, Rong A, Wiezorek J, Sidhu R, Patterson SD. Panitumumab-FOLFOX4 treatment and RAS mutations in colorectal cancer. N Engl J Med. 2013 Sep 12;369(11):1023-34. [https://doi.org/10.1056/NEJMoa1305275 link to original article] [https://pubmed.ncbi.nlm.nih.gov/24024839 PubMed]
+
# '''GOG0209:''' Miller DS, Filiaci VL, Mannel RS, Cohn DE, Matsumoto T, Tewari KS, DiSilvestro P, Pearl ML, Argenta PA, Powell MA, Zweizig SL, Warshal DP, Hanjani P, Carney ME, Huang H, Cella D, Zaino R, Fleming GF. Carboplatin and Paclitaxel for Advanced Endometrial Cancer: Final Overall Survival and Adverse Event Analysis of a Phase III Trial (NRG Oncology/GOG0209). J Clin Oncol. 2020 Nov 20;38(33):3841-3850. Epub 2020 Sep 29. [https://doi.org/10.1200/jco.20.01076 link to original article] '''contains dosing details in manuscript''' [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7676887/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/33078978/ PubMed] NCT00063999
##'''Update:''' Douillard JY, Siena S, Cassidy J, Tabernero J, Burkes R, Barugel M, Humblet Y, Bodoky G, Cunningham D, Jassem J, Rivera F, Kocákova I, Ruff P, Błasińska-Morawiec M, Smakal M, Canon JL, Rother M, Oliner KS, Tian Y, Xu F, Sidhu R. Final results from PRIME: randomized phase III study of panitumumab with FOLFOX4 for first-line treatment of metastatic colorectal cancer. Ann Oncol. 2014 Jul;25(7):1346-55. Epub 2014 Apr 8. [https://doi.org/10.1093/annonc/mdu141 link to original article] [https://pubmed.ncbi.nlm.nih.gov/24718886 PubMed]
+
# '''GOG-0261:''' Powell MA, Filiaci VL, Hensley ML, Huang HQ, Moore KN, Tewari KS, Copeland LJ, Secord AA, Mutch DG, Santin A, Warshal DP, Spirtos NM, DiSilvestro PA, Ioffe OB, Miller DS. Randomized Phase III Trial of Paclitaxel and Carboplatin Versus Paclitaxel and Ifosfamide in Patients With Carcinosarcoma of the Uterus or Ovary: An NRG Oncology Trial. J Clin Oncol. 2022 Mar 20;40(9):968-977. Epub 2022 Jan 10. [https://doi.org/10.1200/jco.21.02050 link to original article] '''contains dosing details in manuscript''' [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8937015/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/35007153/ PubMed] NCT00954174
#'''TAILOR:''' Qin S, Li J, Wang L, Xu J, Cheng Y, Bai Y, Li W, Xu N, Lin LZ, Wu Q, Li Y, Yang J, Pan H, Ouyang X, Qiu W, Wu K, Xiong J, Dai G, Liang H, Hu C, Zhang J, Tao M, Yao Q, Wang J, Chen J, Eggleton SP, Liu T. Efficacy and tolerability of first-line cetuximab plus leucovorin, fluorouracil, and oxaliplatin (FOLFOX-4) versus FOLFOX-4 in patients with RAS wild-type metastatic colorectal cancer: the open-label, randomized, phase III TAILOR trial. J Clin Oncol. 2018 Oct 20;36(30):3031-9. Epub 2018 Sep 10. [https://doi.org/10.1200/JCO.2018.78.3183 link to original article] '''contains dosing details in abstract''' [https://pubmed.ncbi.nlm.nih.gov/30199311 PubMed] NCT01228734
+
# '''RUBY:''' NCT03981796
==FOLFOX4 & Cetuximab {{#subobject:5e5bf3|Regimen=1}}==
+
==Carboplatin & Paclitaxel (CP) & Trastuzumab {{#subobject:b0ejgf|Regimen=1}}==
FOLFOX4 & Cetuximab: '''<u>FOL</u>'''inic acid, '''<u>F</u>'''luorouracil, '''<u>OX</u>'''aliplatin, Cetuximab
+
CP+T: '''<u>C</u>'''arboplatin, '''<u>P</u>'''aclitaxel, '''<u>T</u>'''rastuzumab
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen {{#subobject:9ec84d|Variant=1}}===
+
===Regimen {{#subobject:7ab110|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
Line 453: Line 521:
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
|-
 
|-
|[https://doi.org/10.1200/JCO.2008.20.8397 Bokemeyer et al. 2008 (OPUS)]
+
|[https://doi.org/10.1200/jco.2017.76.5966 Fader et al. 2018]
|2005-2006
+
|2011-2017
 
| style="background-color:#1a9851" |Randomized Phase 2 (E-esc)
 
| style="background-color:#1a9851" |Randomized Phase 2 (E-esc)
|[[#FOLFOX4|FOLFOX4]]
+
|[[#Carboplatin_.26_Paclitaxel_.28CP.29|CP]]
| style="background-color:#1a9850" |Superior OS<sup>1</sup><br>Median OS: 23.5 vs 19.5 mo<br>(HR 0.81, 95% CI 0.69-0.94)
+
| style="background-color:#1a9850" |Superior PFS<sup>1</sup><br>Median PFS: 12.9 vs 8 mo<br>(HR 0.46, 90% CI 0.28-0.76)
|-
 
|[https://doi.org/10.1200/JCO.2018.78.3183 Qin et al. 2018 (TAILOR-CRC)]
 
|2010-NR
 
| style="background-color:#1a9851" |Phase 3 (E-esc)
 
|[[#FOLFOX4|FOLFOX4]]
 
| style="background-color:#91cf60" |Seems to have superior OS<br>Median OS: 20.7 vs 17.8 mo<br>(HR 0.76, 95% CI 0.61-0.96)
 
 
|-
 
|-
 
|}
 
|}
''<sup>1</sup>Reported efficacy for OPUS is based on the 2012 pooled update and is only for KRAS wild-type tumors.''<br>
+
''<sup>1</sup>Reported efficacy is based on the 2020 update.''
''TAILOR required RAS wild-type (not just KRAS). Note that there is another trial named TAILOR in non-small cell lung cancer, so this one has been dubbed TAILOR-CRC.''
 
 
<div class="toccolours" style="background-color:#fdcdac">
 
<div class="toccolours" style="background-color:#fdcdac">
 
====Biomarker eligibility criteria====
 
====Biomarker eligibility criteria====
*OPUS: none
+
*HER2 overexpression
*TAILOR-CRC: Wild-type KRAS, Wild-type NRAS
 
 
</div>
 
</div>
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
*[[Folinic acid (Leucovorin)]] 200 mg/m<sup>2</sup> IV over 2 hours once per day on days 1 & 2, '''given second, with oxaliplatin on day 1'''
+
*[[Carboplatin (Paraplatin)]] as follows:
*[[Fluorouracil (5-FU)]] 400 mg/m<sup>2</sup> IV bolus once per day on days 1 & 2, then 600 mg/m<sup>2</sup> IV continuous infusion over 22 hours after each bolus, '''given third''' (total dose per cycle: 2000 mg/m<sup>2</sup>)
+
**Cycles 1 to 6: AUC 5 IV once on day 1
*[[Oxaliplatin (Eloxatin)]] 85 mg/m<sup>2</sup> IV over 2 hours once on day 1, '''given second'''
+
*[[Paclitaxel (Taxol)]] as follows:
 +
**Cycles 1 to 6: 175 mg/m<sup>2</sup> IV over 3 hours once on day 1
 
====Targeted therapy====
 
====Targeted therapy====
*[[Cetuximab (Erbitux)]] '''given first''', as follows:
+
*[[Trastuzumab (Herceptin)]] as follows:
**Cycle 1: 400 mg/m<sup>2</sup> IV over 2 hours once on day 1, then 250 mg/m<sup>2</sup> IV over 60 minutes once on day 8
+
**Cycle 1: 8 mg/kg IV once on day 1
**Cycle 2 onwards: 250 mg/m<sup>2</sup> IV over 60 minutes once per day on days 1 & 8
+
**Cycle 2 onwards: 6 mg/kg IV once on day 1
'''14-day cycles'''
+
'''21-day cycles'''
 
</div></div>
 
</div></div>
 
===References===
 
===References===
#'''OPUS:''' Bokemeyer C, Bondarenko I, Makhson A, Hartmann JT, Aparicio J, de Braud F, Donea S, Ludwig H, Schuch G, Stroh C, Loos AH, Zubel A, Koralewski P. Fluorouracil, leucovorin, and oxaliplatin with and without cetuximab in the first-line treatment of metastatic colorectal cancer. J Clin Oncol. 2009 Feb 10;27(5):663-71. Epub 2008 Dec 29. [https://doi.org/10.1200/JCO.2008.20.8397 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/19114683 PubMed] NCT00125034
+
#Fader AN, Roque DM, Siegel E, Buza N, Hui P, Abdelghany O, Chambers SK, Secord AA, Havrilesky L, O'Malley DM, Backes F, Nevadunsky N, Edraki B, Pikaart D, Lowery W, ElSahwi KS, Celano P, Bellone S, Azodi M, Litkouhi B, Ratner E, Silasi DA, Schwartz PE, Santin AD. Randomized Phase II Trial of Carboplatin-Paclitaxel Versus Carboplatin-Paclitaxel-Trastuzumab in Uterine Serous Carcinomas That Overexpress Human Epidermal Growth Factor Receptor 2/neu. J Clin Oncol. 2018 Jul 10;36(20):2044-2051. Epub 2018 Mar 27. [https://doi.org/10.1200/jco.2017.76.5966 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/29584549/ PubMed] NCT01367002
##'''Update:''' Bokemeyer C, Bondarenko I, Hartmann JT, de Braud F, Schuch G, Zubel A, Celik I, Schlichting M, Koralewski P. Efficacy according to biomarker status of cetuximab plus FOLFOX-4 as first-line treatment for metastatic colorectal cancer: the OPUS study. Ann Oncol. 2011 Jul;22(7):1535-46. Epub 2011 Jan 12. [https://doi.org/10.1093/annonc/mdq632 link to original article] [https://pubmed.ncbi.nlm.nih.gov/21228335 PubMed]
+
##'''Update:''' Fader AN, Roque DM, Siegel E, Buza N, Hui P, Abdelghany O, Chambers S, Secord AA, Havrilesky L, O'Malley DM, Backes FJ, Nevadunsky N, Edraki B, Pikaart D, Lowery W, ElSahwi K, Celano P, Bellone S, Azodi M, Litkouhi B, Ratner E, Silasi DA, Schwartz PE, Santin AD. Randomized Phase II Trial of Carboplatin-Paclitaxel Compared with Carboplatin-Paclitaxel-Trastuzumab in Advanced (Stage III-IV) or Recurrent Uterine Serous Carcinomas that Overexpress Her2/Neu (NCT01367002): Updated Overall Survival Analysis. Clin Cancer Res. 2020 Aug 1;26(15):3928-3935. Epub 2020 Jun 29. [https://doi.org/10.1158/1078-0432.ccr-20-0953 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/pmc8792803/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/32601075/ PubMed]
##'''Pooled update:''' Bokemeyer C, Van Cutsem E, Rougier P, Ciardiello F, Heeger S, Schlichting M, Celik I, Köhne CH. Addition of cetuximab to chemotherapy as first-line treatment for KRAS wild-type metastatic colorectal cancer: Pooled analysis of the CRYSTAL and OPUS randomised clinical trials. Eur J Cancer. 2012 Jul;48(10):1466-75. Epub 2012 Mar 23. [https://www.ejcancer.com/article/S0959-8049(12)00209-2 link to original article] [https://pubmed.ncbi.nlm.nih.gov/22446022 PubMed]
+
==Carboplatin & Pegylated liposomal doxorubicin {{#subobject:c8ff00|Regimen=1}}==
#'''TAILOR:''' Qin S, Li J, Wang L, Xu J, Cheng Y, Bai Y, Li W, Xu N, Lin LZ, Wu Q, Li Y, Yang J, Pan H, Ouyang X, Qiu W, Wu K, Xiong J, Dai G, Liang H, Hu C, Zhang J, Tao M, Yao Q, Wang J, Chen J, Eggleton SP, Liu T. Efficacy and tolerability of first-line cetuximab plus leucovorin, fluorouracil, and oxaliplatin (FOLFOX-4) versus FOLFOX-4 in patients with RAS wild-type metastatic colorectal cancer: the open-label, randomized, phase III TAILOR trial. J Clin Oncol. 2018 Oct 20;36(30):3031-9. Epub 2018 Sep 10. [https://doi.org/10.1200/JCO.2018.78.3183 link to original article] '''contains dosing details in abstract''' [https://pubmed.ncbi.nlm.nih.gov/30199311 PubMed] NCT01228734
 
==FOLFOX4 & Panitumumab {{#subobject:486271|Regimen=1}}==
 
FOLFOX4 & Panitumumab: '''<u>FOL</u>'''inic acid, '''<u>F</u>'''luorouracil, '''<u>OX</u>'''aliplatin, Panitumumab
 
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen {{#subobject:d862a3|Variant=1}}===
+
===Regimen {{#subobject:d48f39|Variant=1}}===
 +
{| class="wikitable" style="width: 40%; text-align:center;"
 +
!style="width: 25%"|Study
 +
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 +
|-
 +
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2359926/ Pignata et al. 2007 (END-1)]
 +
|style="background-color:#91cf61"|Phase 2
 +
|-
 +
|}
 +
''Note: All patients received 3 cycles of therapy. If there was no unacceptable toxicity, patients with stable or responsive disease received an additional 3 cycles.''
 +
<div class="toccolours" style="background-color:#b3e2cd">
 +
====Chemotherapy====
 +
*[[Carboplatin (Paraplatin)]] AUC 5 IV over 30 minutes once on day 1, '''given first'''
 +
*[[Pegylated liposomal doxorubicin (Doxil)]] 40 mg/m<sup>2</sup> IV over 60 minutes once on day 1, '''given second'''
 +
====Supportive therapy====
 +
*[[:Category:Granulocyte colony-stimulating factors|G-CSF]] by the following criteria:
 +
**Prophylaxis: not recommended
 +
**Grade 4 neutropenia: therapeutic and prophylactic use was allowed
 +
'''28-day cycle for 3 to 6 cycles'''
 +
</div></div>
 +
===References===
 +
# '''END-1:''' Pignata S, Scambia G, Pisano C, Breda E, Di Maio M, Greggi S, Ferrandina G, Lorusso D, Zagonel V, Febbraro A, Riva N, De Rosa V, Gallo C, Perrone F; Multicentre Italian Trials in Ovarian Cancer and Gynecologic Malignancies Group. A multicentre phase II study of carboplatin plus pegylated liposomal doxorubicin as first-line chemotherapy for patients with advanced or recurrent endometrial carcinoma: the END-1 study of the MITO (Multicentre Italian Trials in Ovarian Cancer and Gynecologic Malignancies) group. Br J Cancer. 2007 Jun 4;96(11):1639-43. Epub 2007 May 8. [https://doi.org/10.1038/sj.bjc.6603787 link to original article] '''contains dosing details in manuscript''' [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2359926/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/17486128 PubMed]
 +
==CIM {{#subobject:ac4ecc|Regimen=1}}==
 +
CIM: '''<u>C</u>'''isplatin, '''<u>I</u>'''fosfamide, '''<u>M</u>'''esna
 +
<div class="toccolours" style="background-color:#eeeeee">
 +
===Regimen {{#subobject:a26ea4|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
Line 500: Line 583:
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
|-
 
|-
|[https://doi.org/10.1200/jco.2009.27.4860 Douillard et al. 2010 (PRIME)]
+
|[https://www.gynecologiconcology-online.net/article/S0090-8258(00)96001-3/pdf Sutton et al. 2000 (GOG 108)]
|2006-2008 (C)
+
|1989-1996
| style="background-color:#1a9851" |Phase 3 (E-RT-esc)
+
|style="background-color:#1a9851"|Phase 3 (E-esc)
|[[#FOLFOX4|FOLFOX4]]
+
|[[#Ifosfamide_monotherapy|Ifosfamide]]
| style="background-color:#91cf60" |Seems to have superior OS<sup>1</sup><br>Median OS: 23.8 vs 19.4 mo<br>(HR 0.83, 95% CI 0.70-0.98)
+
| style="background-color:#91cf60" |Seems to have superior PFS
 
|-
 
|-
 
|}
 
|}
''<sup>1</sup>In KRAS wild-type patients, this regimen seems to have superior OS, based on the exploratory analysis in the 2014 update.''
 
<div class="toccolours" style="background-color:#fdcdac">
 
====Biomarker eligibility criteria====
 
*Wild-type KRAS, Wild-type NRAS
 
</div>
 
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
*[[Fluorouracil (5-FU)]] 400 mg/m<sup>2</sup> IV bolus once per day on days 1 & 2, then 600 mg/m<sup>2</sup> IV continuous infusion over 22 hours after each bolus (total dose per cycle: 2000 mg/m<sup>2</sup>)
+
*[[Cisplatin (Platinol)]]
*[[Folinic acid (Leucovorin)]] 200 mg/m<sup>2</sup> IV over 2 hours once per day on days 1 & 2
+
*[[Ifosfamide (Ifex)]]
*[[Oxaliplatin (Eloxatin)]] 85 mg/m<sup>2</sup> IV over 2 hours once on day 1
+
====Supportive therapy====
====Targeted therapy====
+
*[[Mesna (Mesnex)]]
*[[Panitumumab (Vectibix)]] 6 mg/kg IV once on day 1, '''given first'''
 
**Infusion times are 1 hour for cycle 1, then if tolerated, 30 minutes for cycle 2 and later
 
'''14-day cycles'''
 
 
</div></div>
 
</div></div>
 
===References===
 
===References===
<!-- Presented in part at the 43rd Annual Meeting of the American Society of Clinical Oncology, June 1-5, 2007, Chicago, IL; the 2008 Gastrointestinal Cancers Symposium, January 25-27, 2008, Orlando, FL; the joint 15th Congress of the European Cancer Organisation and 34th Congress of the European Society for Medical Oncology, September 20-24, 2009, Berlin, Germany; the 6th Annual Meeting of the International Society of Gastrointestinal Oncology, October 1-3, 2009, Philadelphia, PA; the 2009 National Cancer Research Institute Cancer Conference, October 4-7, 2009, Birmingham, United Kingdom; and the 2010 Gastrointestinal Cancers Symposium, January 22-24, 2010, Orlando, FL. -->
+
# '''GOG 108:''' Sutton G, Brunetto VL, Kilgore L, Soper JT, McGehee R, Olt G, Lentz SS, Sorosky J, Hsiu JG. A phase III trial of ifosfamide with or without cisplatin in carcinosarcoma of the uterus: A Gynecologic Oncology Group study. Gynecol Oncol. 2000 Nov;79(2):147-53. [https://www.gynecologiconcology-online.net/article/S0090-8258(00)96001-3/pdf link to original article] [https://pubmed.ncbi.nlm.nih.gov/11063636 PubMed]
#'''PRIME:''' Douillard JY, Siena S, Cassidy J, Tabernero J, Burkes R, Barugel M, Humblet Y, Bodoky G, Cunningham D, Jassem J, Rivera F, Kocákova I, Ruff P, Błasińska-Morawiec M, Šmakal M, Canon JL, Rother M, Oliner KS, Wolf M, Gansert J. Randomized, phase III trial of panitumumab with infusional fluorouracil, leucovorin, and oxaliplatin (FOLFOX4) versus FOLFOX4 alone as first-line treatment in patients with previously untreated metastatic colorectal cancer: the PRIME study. J Clin Oncol. 2010 Nov 1;28(31):4697-705. Epub 2010 Oct 4. [https://doi.org/10.1200/jco.2009.27.4860 link to original article] [https://pubmed.ncbi.nlm.nih.gov/20921465 PubMed] NCT00364013
+
==Cisplatin & Doxorubicin {{#subobject:7f9e48|Regimen=1}}==
##'''Biomarker analysis:''' Douillard JY, Oliner KS, Siena S, Tabernero J, Burkes R, Barugel M, Humblet Y, Bodoky G, Cunningham D, Jassem J, Rivera F, Kocákova I, Ruff P, Błasińska-Morawiec M, Šmakal M, Canon JL, Rother M, Williams R, Rong A, Wiezorek J, Sidhu R, Patterson SD. Panitumumab-FOLFOX4 treatment and RAS mutations in colorectal cancer. N Engl J Med. 2013 Sep 12;369(11):1023-34. [https://doi.org/10.1056/NEJMoa1305275 link to original article] [https://pubmed.ncbi.nlm.nih.gov/24024839 PubMed]
+
AP: '''<u>A</u>'''driamycin (Doxorubicin) & '''<u>P</u>'''latinol (Cisplatin)
##'''Update:''' Douillard JY, Siena S, Cassidy J, Tabernero J, Burkes R, Barugel M, Humblet Y, Bodoky G, Cunningham D, Jassem J, Rivera F, Kocákova I, Ruff P, Błasińska-Morawiec M, Smakal M, Canon JL, Rother M, Oliner KS, Tian Y, Xu F, Sidhu R. Final results from PRIME: randomized phase III study of panitumumab with FOLFOX4 for first-line treatment of metastatic colorectal cancer. Ann Oncol. 2014 Jul;25(7):1346-55. Epub 2014 Apr 8. [https://doi.org/10.1093/annonc/mdu141 link to original article] [https://pubmed.ncbi.nlm.nih.gov/24718886 PubMed]
 
==mFOLFOX6-B {{#subobject:8ugz86|Regimen=1}}==
 
mFOLFOX6-B: '''<u>m</u>'''odified '''<u>FOL</u>'''inic acid, '''<u>F</u>'''luorouracil, '''<u>OX</u>'''aliplatin, '''<u>B</u>'''evacizumab
 
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen {{#subobject:8baf2c|Variant=1}}===
+
===Regimen variant #1, 50/45 {{#subobject:1748e2|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
Line 538: Line 610:
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
|-
 
|-
|rowspan=2|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5545896/ Venook et al. 2017 (CALGB 80405)]
+
|[https://doi.org/10.1200/jco.2004.07.184 Fleming et al. 2004a (GOG 177)]
|rowspan=2|2005-2012
+
|1998-2000
|rowspan=2 style="background-color:#1a9851" |Phase 3 (E-switch-ic)
+
|style="background-color:#1a9851"|Phase 3 (C)
|1. [[#mFOLFOX6_.26_Panitumumab|mFOLFOX6 & Panitumumab]]<br>2. [[#FOLFIRI_.26_Panitumumab_88|FOLFIRI & Panitumumab]]
+
|[[#Cisplatin.2C_Doxorubicin.2C_Paclitaxel|Cisplatin, Doxorubicin, Paclitaxel]]
| style="background-color:#ffffbf" |Did not meet primary endpoint of OS
+
|style="background-color:#fc8d59"|Seems to have inferior OS
 
|-
 
|-
|3. [[#mFOLFOX6.2C_Bevacizumab.2C_Cetuximab_99|mFOLFOX6, Bevacizumab, Cetuximab]]<br>4. [[#FOLFIRI.2C_Bevacizumab.2C_Cetuximab_99|FOLFIRI, Bevacizumab, Cetuximab]]
+
|}
| style="background-color:#d3d3d3" |Not reported
+
''Note: body surface area was capped at 2 m<sup>2</sup>. This dosage was for patients with previous pelvic radiation or who were greater than 65 years old.''
 +
<div class="toccolours" style="background-color:#b3e2cd">
 +
====Chemotherapy====
 +
*[[Cisplatin (Platinol)]] 50 mg/m<sup>2</sup> (maximum dose of 100 mg) IV over 60 minutes once on day 1, '''given second'''
 +
*[[Doxorubicin (Adriamycin)]] 45 mg/m<sup>2</sup> (maximum dose of 90 mg) IV once on day 1, '''given first'''
 +
'''21-day cycle for 7 cycles'''
 +
</div></div><br>
 +
<div class="toccolours" style="background-color:#eeeeee">
 +
===Regimen variant #2, 50/60, capped BSA {{#subobject:3b1876|Variant=1}}===
 +
{| class="wikitable sortable" style="width: 100%; text-align:center;"
 +
!style="width: 20%"|Study
 +
!style="width: 20%"|Years of enrollment
 +
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 +
!style="width: 20%"|Comparator
 +
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
|-
 
|-
|Awaiting publication (PARADIGM<sub>CRC</sub>)
+
|[https://doi.org/10.1200/jco.2004.07.184 Fleming et al. 2004a (GOG 177)]
|2015-2022
+
|1998-2000
| style="background-color:#1a9851" |Phase 3 (C)
+
|style="background-color:#1a9851"|Phase 3 (C)
|[[#mFOLFOX6_.26_Panitumumab|mFOLFOX6 & Panitumumab]]
+
|[[#Cisplatin.2C_Doxorubicin.2C_Paclitaxel|Cisplatin, Doxorubicin, Paclitaxel]]
| style="background-color:#fc8d59" |Seems to have inferior OS
+
|style="background-color:#fc8d59"|Seems to have inferior OS
 
|-
 
|-
 
|}
 
|}
 +
''Note: body surface area was capped at 2 m<sup>2</sup>.''
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
*[[Fluorouracil (5-FU)]] 400 mg/m<sup>2</sup> IV bolus once on day 1, then 2400 mg/m<sup>2</sup> IV continuous infusion over 46 hours (total dose per cycle: 2800 mg/m<sup>2</sup>)
+
*[[Cisplatin (Platinol)]] 50 mg/m<sup>2</sup> (maximum dose of 100 mg) IV over 60 minutes once on day 1, '''given second'''
*[[Folinic acid (Leucovorin)]] 200 mg/m<sup>2</sup> IV once on day 1
+
*[[Doxorubicin (Adriamycin)]] 60 mg/m<sup>2</sup> (maximum dose of 120 mg) IV once on day 1, '''given first'''
*[[Oxaliplatin (Eloxatin)]] 85 mg/m<sup>2</sup> IV once on day 1
+
'''21-day cycle for 7 cycles'''
====Targeted therapy====
+
</div></div><br>
*[[Bevacizumab (Avastin)]] 5 mg/kg IV once on day 1
 
'''14-day cycles'''
 
</div></div>
 
===References===
 
#'''CALGB 80405:''' Venook AP, Niedzwiecki D, Lenz HJ, Innocenti F, Fruth B, Meyerhardt JA, Schrag D, Greene C, O'Neil BH, Atkins JN, Berry S, Polite BN, O'Reilly EM, Goldberg RM, Hochster HS, Schilsky RL, Bertagnolli MM, El-Khoueiry AB, Watson P, Benson AB 3rd, Mulkerin DL, Mayer RJ, Blanke C. Effect of First-Line Chemotherapy Combined With Cetuximab or Bevacizumab on Overall Survival in Patients With KRAS Wild-Type Advanced or Metastatic Colorectal Cancer: A Randomized Clinical Trial. JAMA. 2017 Jun 20;317(23):2392-2401. [https://jamanetwork.com/journals/jama/fullarticle/2632502 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5545896/ link to PMC article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/28632865 PubMed] NCT00265850
 
#'''PARADIGM<sub>CRC</sub>:''' NCT02394795
 
==mFOLFOX6 & Cetuximab {{#subobject:12d786|Regimen=1}}==
 
mFOLFOX6 & Cetuximab: '''<u>m</u>'''odified '''<u>FOL</u>'''inic acid, '''<u>F</u>'''luorouracil, '''<u>OX</u>'''aliplatin, Cetuximab
 
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen {{#subobject:8baf2c|Variant=1}}===
+
===Regimen variant #3, 50/60, no cap on BSA {{#subobject:5baa3b|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
Line 577: Line 656:
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
|-
 
|-
|rowspan=2|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5545896/ Venook et al. 2017 (CALGB 80405)]
+
|[https://doi.org/10.1093/annonc/mdh316 Fleming et al. 2004 (GOG 163)]
|rowspan=2|2005-2012
+
|1996-1998
|rowspan=2 style="background-color:#1a9851" |Phase 3 (E-switch-ic)
+
|style="background-color:#1a9851"|Phase 3 (C)
|1. [[#mFOLFOX6_.26_Panitumumab|mFOLFOX6 & Panitumumab]]<br>2. [[#FOLFIRI_.26_Panitumumab_88|FOLFIRI & Panitumumab]]
+
|[[#Doxorubicin_.26_Paclitaxel_.28AT.29_99|Doxorubicin & Paclitaxel]]
| style="background-color:#ffffbf" |Did not meet primary endpoint of OS
+
| style="background-color:#ffffbf" |Did not meet primary endpoint of ORR
 +
|-
 +
|[https://doi.org/10.1200/JCO.2004.02.088 Thigpen et al. 2004 (GOG 107)]
 +
|NR
 +
|style="background-color:#1a9851"|Phase 3 (E-esc)
 +
|[[#Doxorubicin_monotherapy|Doxorubicin]]
 +
| style="background-color:#91cf60" |Seems to have superior PFS
 
|-
 
|-
|3. [[#mFOLFOX6.2C_Bevacizumab.2C_Cetuximab_99|mFOLFOX6, Bevacizumab, Cetuximab]]<br>4. [[#FOLFIRI.2C_Bevacizumab.2C_Cetuximab_99|FOLFIRI, Bevacizumab, Cetuximab]]
+
|}
| style="background-color:#d3d3d3" |Not reported
+
<div class="toccolours" style="background-color:#b3e2cd">
 +
====Chemotherapy====
 +
*[[Cisplatin (Platinol)]] 50 mg/m<sup>2</sup> IV once on day 1
 +
*[[Doxorubicin (Adriamycin)]] 60 mg/m<sup>2</sup> IV once on day 1
 +
====Supportive therapy====
 +
*Normal saline at 500 mL/H for 2 hours prior to and after [[Cisplatin (Platinol)]]
 +
'''21-day cycle for up to 8 cycles'''
 +
</div></div><br>
 +
<div class="toccolours" style="background-color:#eeeeee">
 +
===Regimen variant #4, 60/60 {{#subobject:828296|Variant=1}}===
 +
{| class="wikitable sortable" style="width: 100%; text-align:center;"
 +
!style="width: 20%"|Study
 +
!style="width: 20%"|Years of enrollment
 +
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 +
!style="width: 20%"|Comparator
 +
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
|-
 
|-
|[https://www.ejcancer.com/article/S0959-8049(18)30938-9 Aranda et al. 2018 (MACRO-2)]
+
|[https://doi.org/10.1200/JCO.2003.10.083 Gallion et al. 2003 (GOG 139)]
|2010-NR
+
|1993-1996
| style="background-color:#91cf61" |Non-randomized portion of phase 2 RCT
+
|style="background-color:#1a9851"|Phase 3 (C)
| style="background-color:#d3d3d3" |
+
|[[#Cisplatin_.26_Doxorubicin_2|Cisplatin & Doxorubicin]]; chronomodulated
| style="background-color:#d3d3d3" |
+
| style="background-color:#ffffbf" |Did not meet primary endpoint of ORR
 
|-
 
|-
 
|}
 
|}
''Note: In CALGB 80405, the arm receiving bevacizumab and cetuximab was terminated early.''
 
<div class="toccolours" style="background-color:#fdcdac">
 
====Biomarker eligibility criteria====
 
*CALGB 80405: Wild-type KRAS (codons 12 & 13)
 
*MACRO-2: Wild-type KRAS (exons 3 & 4), Wild-type NRAS (exons 2 to 4)
 
</div>
 
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
*[[Fluorouracil (5-FU)]] 400 mg/m<sup>2</sup> IV bolus once on day 1, then 2400 mg/m<sup>2</sup> IV continuous infusion over 46 hours (total dose per cycle: 2800 mg/m<sup>2</sup>)
+
*[[Cisplatin (Platinol)]] 60 mg/m<sup>2</sup> IV once on day 1
*[[Folinic acid (Leucovorin)]] 400 mg/m<sup>2</sup> IV once on day 1
+
*[[Doxorubicin (Adriamycin)]] 60 mg/m<sup>2</sup> IV once on day 1
*[[Oxaliplatin (Eloxatin)]] 85 mg/m<sup>2</sup> IV once on day 1
+
'''21-day cycle for up to 8 cycles'''
====Targeted therapy====
 
*[[Cetuximab (Erbitux)]] as follows, '''given first''':
 
**Cycle 1: 400 mg/m<sup>2</sup> IV once on day 1, then 250 mg/m<sup>2</sup> IV once on day 8
 
**Cycle 2 onwards: 250 mg/m<sup>2</sup> IV once per day on days 1 & 8
 
'''14-day cycles (see below)'''
 
</div>
 
<div class="toccolours" style="background-color:#cbd5e7">
 
====Subsequent treatment====
 
*MACRO-2, after 8 cycles: continued [[#mFOLFOX6_.26_Cetuximab_2|mFOLFOX6 & Cetuximab]] until progression versus [[#Cetuximab_monotherapy|cetuximab]] maintenance
 
 
</div></div>
 
</div></div>
 
===References===
 
===References===
#'''CALGB 80405:''' Venook AP, Niedzwiecki D, Lenz HJ, Innocenti F, Fruth B, Meyerhardt JA, Schrag D, Greene C, O'Neil BH, Atkins JN, Berry S, Polite BN, O'Reilly EM, Goldberg RM, Hochster HS, Schilsky RL, Bertagnolli MM, El-Khoueiry AB, Watson P, Benson AB 3rd, Mulkerin DL, Mayer RJ, Blanke C. Effect of First-Line Chemotherapy Combined With Cetuximab or Bevacizumab on Overall Survival in Patients With KRAS Wild-Type Advanced or Metastatic Colorectal Cancer: A Randomized Clinical Trial. JAMA. 2017 Jun 20;317(23):2392-2401. [https://jamanetwork.com/journals/jama/fullarticle/2632502 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5545896/ link to PMC article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/28632865 PubMed] NCT00265850
+
# '''GOG 139:''' Gallion HH, Brunetto VL, Cibull M, Lentz SS, Reid G, Soper JT, Burger RA, Andersen W; Gynecologic Oncology Group. Randomized phase III trial of standard timed doxorubicin plus cisplatin versus circadian timed doxorubicin plus cisplatin in stage III and IV or recurrent endometrial carcinoma: a Gynecologic Oncology Group study. J Clin Oncol. 2003 Oct 15;21(20):3808-13. [https://doi.org/10.1200/JCO.2003.10.083 link to original article] '''contains dosing details in abstract''' [https://pubmed.ncbi.nlm.nih.gov/14551299 PubMed]
#'''MACRO-2:''' Aranda E, García-Alfonso P, Benavides M, Sánchez Ruiz A, Guillén-Ponce C, Safont MJ, Alcaide J, Gómez A, López R, Manzano JL, Méndez Ureña M, Sastre J, Rivera F, Grávalos C, García T, Martín-Valadés JI, Falcó E, Navalón M, González Flores E, Ma García Tapiador A, Ma López Muñoz A, Barrajón E, Reboredo M, García Teijido P, Viudez A, Cárdenas N, Díaz-Rubio E; Spanish Cooperative Group for the Treatment of Digestive Tumours. First-line mFOLFOX plus cetuximab followed by mFOLFOX plus cetuximab or single-agent cetuximab as maintenance therapy in patients with metastatic colorectal cancer: phase II randomised MACRO2 TTD study. Eur J Cancer. 2018 Sep;101:263-272. Epub 2018 Jul 24. [https://www.ejcancer.com/article/S0959-8049(18)30938-9 link to original article] [https://pubmed.ncbi.nlm.nih.gov/30054049 PubMed] NCT01161316
+
# '''GOG 177:''' Fleming GF, Brunetto VL, Cella D, Look KY, Reid GC, Munkarah AR, Kline R, Burger RA, Goodman A, Burks RT. Phase III trial of doxorubicin plus cisplatin with or without paclitaxel plus filgrastim in advanced endometrial carcinoma: a Gynecologic Oncology Group study. J Clin Oncol. 2004 Jun 1;22(11):2159-66. [https://doi.org/10.1200/jco.2004.07.184 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/15169803 PubMed] NCT00003691
==mFOLFOX6 & Panitumumab {{#subobject:avn786|Regimen=1}}==
+
# '''GOG 163:''' Fleming GF, Filiaci VL, Bentley RC, Herzog T, Sorosky J, Vaccarello L, Gallion H. Phase III randomized trial of doxorubicin + cisplatin versus doxorubicin + 24-h paclitaxel + filgrastim in endometrial carcinoma: a Gynecologic Oncology Group study. Ann Oncol. 2004 Aug;15(8):1173-8. [https://doi.org/10.1093/annonc/mdh316 link to original article] '''contains dosing details in abstract''' [https://pubmed.ncbi.nlm.nih.gov/15277255 PubMed]
mFOLFOX6 & Panitumumab: '''<u>m</u>'''odified '''<u>FOL</u>'''inic acid, '''<u>F</u>'''luorouracil, '''<u>OX</u>'''aliplatin, Panitumumab
+
# '''GOG 107:''' Thigpen JT, Brady MF, Homesley HD, Malfetano J, DuBeshter B, Burger RA, Liao S. Phase III trial of doxorubicin with or without cisplatin in advanced endometrial carcinoma: a Gynecologic Oncology Group study. J Clin Oncol. 2004 Oct 1;22(19):3902-8. [https://doi.org/10.1200/JCO.2004.02.088 link to original article] '''contains dosing details in abstract''' [https://pubmed.ncbi.nlm.nih.gov/15459211 PubMed]
 +
==Cisplatin, Doxorubicin, Paclitaxel {{#subobject:b61c1e|Regimen=1}}==
 +
TAP: '''<u>T</u>'''axol (Paclitaxel), '''<u>A</u>'''driamycin (Doxorubicin), '''<u>P</u>'''latinol (Cisplatin)
 +
<br>CDP: '''<u>C</u>'''isplatin, '''<u>D</u>'''oxorubicin, '''<u>P</u>'''aclitaxel
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen {{#subobject:8bukqc|Variant=1}}===
+
===Regimen {{#subobject:68777b|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
Line 628: Line 716:
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
|-
 
|-
|[http://www.ncbi.nlm.nih.gov/pmc/articles/pmc9426812/ Rossini et al. 2022 (TRIPLETE)]
+
|[https://doi.org/10.1200/jco.2004.07.184 Fleming et al. 2004 (GOG 177)]
|2017-2021
+
|1998-2000
 +
|style="background-color:#1a9851"|Phase 3 (E-esc)
 +
|[[#Cisplatin_.26_Doxorubicin_2|Cisplatin & Doxorubicin]]
 +
|style="background-color:#91cf60"|Seems to have superior OS<br>Median OS: 15.3 vs 12.3 mo<br>(HR 0.75, 95% CI 0.57-0.99)
 +
|-
 +
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7676887/ Miller et al. 2020 (GOG0209)]
 +
|2003-2009
 
| style="background-color:#1a9851" |Phase 3 (C)
 
| style="background-color:#1a9851" |Phase 3 (C)
|[[#mFOLFOXIRI_.26_Panitumumab_99|mFOLFOXIRI & Panitumumab]]
+
|[[#Carboplatin_.26_Paclitaxel_.28CP.29_2|TC]]
| style="background-color:#ffffbf" |Did not meet primary endpoint of ORR
+
| style="background-color:#eeee01" |Non-inferior OS
 
|-
 
|-
 
|}
 
|}
<div class="toccolours" style="background-color:#fdcdac">
+
''Note: in GOG 177, body surface area was capped at 2 m<sup>2</sup>.''
====Biomarker eligibility criteria====
 
*Wild-type KRAS (exons 2 to 4), wild-type NRAS (exons 2 to 4), wild-type BRAF codon 600
 
</div>
 
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
*[[Fluorouracil (5-FU)]] 400 mg/m<sup>2</sup> IV bolus once on day 1, '''given third''', then 2400 mg/m<sup>2</sup> IV continuous infusion over 48 hours (total dose per cycle: 2800 mg/m<sup>2</sup>)
+
*[[Cisplatin (Platinol)]] 50 mg/m<sup>2</sup> IV over 60 minutes once on day 1, '''given second'''
*[[Folinic acid (Leucovorin)]] 200 mg/m<sup>2</sup> IV once on day 1, '''given second'''
+
*[[Doxorubicin (Adriamycin)]] 45 mg/m<sup>2</sup> IV once on day 1, '''given first'''
*[[Oxaliplatin (Eloxatin)]] 85 mg/m<sup>2</sup> IV over 2 hours once on day 1, '''given second'''
+
*[[Paclitaxel (Taxol)]] 160 mg/m<sup>2</sup> IV over 3 hours once on day 2
====Targeted therapy====
+
====Supportive therapy====
*[[Panitumumab (Vectibix)]] 6 mg/kg IV over 30 to 60 minutes once on day 1, '''given first'''
+
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day on days 3 to 12
'''14-day cycles'''
+
'''21-day cycle for 7 cycles'''
 
</div></div>
 
</div></div>
 
===References===
 
===References===
#'''TRIPLETE:''' Rossini D, Antoniotti C, Lonardi S, Pietrantonio F, Moretto R, Antonuzzo L, Boccaccino A, Morano F, Brugia M, Pozzo C, Marmorino F, Bergamo F, Tamburini E, Passardi A, Randon G, Murgioni S, Borelli B, Buonadonna A, Giordano M, Fontanini G, Conca V, Formica V, Aglietta M, Bordonaro R, Aprile G, Masi G, Boni L, Cremolini C. Upfront Modified Fluorouracil, Leucovorin, Oxaliplatin, and Irinotecan Plus Panitumumab Versus Fluorouracil, Leucovorin, and Oxaliplatin Plus Panitumumab for Patients With RAS/BRAF Wild-Type Metastatic Colorectal Cancer: The Phase III TRIPLETE Study by GONO. J Clin Oncol. 2022 Sep 1;40(25):2878-2888. Epub 2022 Jun 6. [https://doi.org/10.1200/jco.22.00839 link to original article] [http://www.ncbi.nlm.nih.gov/pmc/articles/pmc9426812/ link to PMC article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/35666229/ PubMed] NCT03231722
+
# '''GOG 177:''' Fleming GF, Brunetto VL, Cella D, Look KY, Reid GC, Munkarah AR, Kline R, Burger RA, Goodman A, Burks RT. Phase III trial of doxorubicin plus cisplatin with or without paclitaxel plus filgrastim in advanced endometrial carcinoma: a Gynecologic Oncology Group study. J Clin Oncol. 2004 Jun 1;22(11):2159-66. [https://doi.org/10.1200/jco.2004.07.184 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/15169803 PubMed] NCT00003691
==mFOLFOXIRI & Cetuximab (L-Leucovorin){{#subobject:9bf7|Regimen=1}}==
+
# '''GOG0209:''' Miller DS, Filiaci VL, Mannel RS, Cohn DE, Matsumoto T, Tewari KS, DiSilvestro P, Pearl ML, Argenta PA, Powell MA, Zweizig SL, Warshal DP, Hanjani P, Carney ME, Huang H, Cella D, Zaino R, Fleming GF. Carboplatin and Paclitaxel for Advanced Endometrial Cancer: Final Overall Survival and Adverse Event Analysis of a Phase III Trial (NRG Oncology/GOG0209). J Clin Oncol. 2020 Nov 20;38(33):3841-3850. Epub 2020 Sep 29. [https://doi.org/10.1200/jco.20.01076 link to original article] '''contains dosing details in manuscript''' [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7676887/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/33078978/ PubMed] NCT00063999
mFOLFOXIRI & Cetuximab: '''<u>m</u>'''odified L-'''<u>FOL</u>'''inic acid, '''<u>F</u>'''luorouracil, '''<u>OX</u>'''aliplatin, '''<u>IRI</u>'''notecan, Cetuximab
+
==Cisplatin & Paclitaxel {{#subobject:89fd88|Regimen=1}}==
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen {{#subobject:19365|Variant=1}}===
+
===Regimen {{#subobject:b3c8fd|Variant=1}}===
 
{| class="wikitable" style="width: 40%; text-align:center;"  
 
{| class="wikitable" style="width: 40%; text-align:center;"  
! style="width: 25%" |Study
+
!style="width: 25%"|Study
! style="width: 25%" |[[Levels_of_Evidence#Evidence|Evidence]]
+
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
|-
 
|-
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5885260/ Cremolini et al. 2018 (MACBETH)]
+
|[http://www.gynecologiconcology-online.net/article/S0090-8258(00)95827-X Dimopoulos et al. 2000]
| style="background-color:#91cf61" |Non-randomized portion of phase 2 RCT
+
|style="background-color:#91cf61"|Phase 2
 
|-
 
|-
 
|}
 
|}
''Note: 5-FU instructions are unusual in that no bolus is given.''
 
<div class="toccolours" style="background-color:#fdcdac">
 
====Biomarker eligibility criteria====
 
*Wild-type KRAS, Wild-type NRAS
 
</div>
 
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
*[[Fluorouracil (5-FU)]] 1200 mg/m<sup>2</sup>/day IV continuous infusion over 48 hours, started on day 1, '''given fourth''' (total dose per cycle: 2400 mg/m<sup>2</sup>)
+
*[[Cisplatin (Platinol)]] 75 mg/m<sup>2</sup> IV over 2 hours once on day 1, '''given second'''
*[[Levoleucovorin (Fusilev)]] 200 mg/m<sup>2</sup> IV over 2 hours once on day 1, '''given third, with oxaliplatin'''
+
*[[Paclitaxel (Taxol)]] 175 mg/m<sup>2</sup> IV over 3 hours once on day 1, '''given first'''
*[[Oxaliplatin (Eloxatin)]] 85 mg/m<sup>2</sup> IV over 2 hours once on day 1, '''given third, with L-leucovorin'''
+
====Supportive therapy====
*[[Irinotecan (Camptosar)]] 130 mg/m<sup>2</sup> IV over 60 minutes once on day 1, '''given second'''
+
*[[Dexamethasone (Decadron)]] 20 mg IV or PO for two doses on day 1; 12 and 6 hours prior to [[Paclitaxel (Taxol)]]
====Targeted therapy====
+
*[[Diphenhydramine (Benadryl)]] 25 mg IV once on day 1; 30 minutes prior to [[Paclitaxel (Taxol)]]
*[[Cetuximab (Erbitux)]] 500 mg/m<sup>2</sup> IV over 60 minutes once on day 1, '''given first'''
+
*[[Ranitidine (Zantac)]] 50 mg IV once on day 1; 30 minutes prior to [[Paclitaxel (Taxol)]]
'''14-day cycle for 8 cycles'''
+
*900 mL normal saline mixed with 100 mL mannitol given over 1 hour prior to [[Cisplatin (Platinol)]]
</div>
+
*2 liters NS with potassium & magnesium after [[Cisplatin (Platinol)]]
<div class="toccolours" style="background-color:#cbd5e7">
+
*"Appropriate antiemetics"
====Subsequent treatment====
+
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day, starting on day 5 and continuing until WBC greater than 10,000 x 10<sup>9</sup>/L
*MACBETH, if deemed resectable: [[Surgery#Colorectal_cancer_surgery|Surgery]]
+
'''21-day cycle for up to 6 cycles'''
*MACBETH, if deemed unresectable: [[#Cetuximab_monotherapy|Cetuximab]] versus [[#Bevacizumab_monotherapy_99|bevacizumab]] maintenance
 
 
</div></div>
 
</div></div>
 
===References===
 
===References===
#'''MACBETH:''' Cremolini C, Antoniotti C, Lonardi S, Aprile G, Bergamo F, Masi G, Grande R, Tonini G, Mescoli C, Cardellino GG, Coltelli L, Salvatore L, Corsi DC, Lupi C, Gemma D, Ronzoni M, Dell'Aquila E, Marmorino F, Di Fabio F, Mancini ML, Marcucci L, Fontanini G, Zagonel V, Boni L, Falcone A. Activity and safety of cetuximab plus modified FOLFOXIRI followed by maintenance with cetuximab or bevacizumab for RAS and BRAF wild-type metastatic colorectal cancer: a randomized phase 2 clinical trial. JAMA Oncol. 2018 Apr 1;4(4):529-536. [https://jamanetwork.com/journals/jamaoncology/article-abstract/2672387 link to original article] '''contains dosing details in manuscript''' [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5885260/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/29450468 PubMed] NCT02295930
+
# Dimopoulos MA, Papadimitriou CA, Georgoulias V, Moulopoulos LA, Aravantinos G, Gika D, Karpathios S, Stamatelopoulos S. Paclitaxel and cisplatin in advanced or recurrent carcinoma of the endometrium: long-term results of a phase II multicenter study. Gynecol Oncol. 2000 Jul;78(1):52-7. [http://www.gynecologiconcology-online.net/article/S0090-8258(00)95827-X link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/10873410 PubMed]
==FOLFOXIRI & Panitumumab {{#subobject:9bf7|Regimen=1}}==
+
==Dactinomycin monotherapy {{#subobject:97a01a|Regimen=1}}==
FOLFOXIRI & Panitumumab: '''<u>FOL</u>'''inic acid, '''<u>F</u>'''luorouracil, '''<u>OX</u>'''aliplatin, '''<u>IRI</u>'''notecan, Panitumumab
 
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen {{#subobject:19365|Variant=1}}===
+
===Regimen {{#subobject:2019ab|Variant=1}}===
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
+
{| class="wikitable" style="width: 40%; text-align:center;"  
!style="width: 20%"|Study
+
!style="width: 25%"|Study
!style="width: 20%"|Years of enrollment
+
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 20%"|Comparator
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
 
|-
 
|-
|[https://doi.org/10.1200/JCO.19.01340 Modest et al. 2019 (VOLFI)]
+
|[http://www.gynecologiconcology-online.net/article/S0090-8258(99)95652-4 Moore et al. 1999]
|2011-2016
+
|style="background-color:#91cf61"|Phase 2
| style="background-color:#1a9851" |Randomized Phase 2 (E-esc)
 
|[[#FOLFIRINOX|FOLFOXIRI]]
 
| style="background-color:#1a9850" |Superior ORR
 
 
|-
 
|-
 
|}
 
|}
<div class="toccolours" style="background-color:#fdcdac">
 
====Biomarker eligibility criteria====
 
*Wild-type KRAS, Wild-type NRAS
 
</div>
 
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
*[[Fluorouracil (5-FU)]] 1500 mg/m<sup>2</sup>/day IV continuous infusion over 48 hours, started on day 1 (total dose per cycle: 3000 mg/m<sup>2</sup>)
+
*[[Dactinomycin (Cosmegen)]] 2 mg/m<sup>2</sup> IV over 15 minutes once on day 1
*[[Folinic acid (Leucovorin)]] 200 mg/m<sup>2</sup> IV once on day 1
+
'''28-day cycles'''
*[[Oxaliplatin (Eloxatin)]] 85 mg/m<sup>2</sup> IV once on day 1
+
</div></div>
*[[Irinotecan (Camptosar)]] 150 mg/m<sup>2</sup> IV once on day 1
+
===References===
====Targeted therapy====
+
# Moore DH, Blessing JA, Dunton C, Buller RE, Reid GC; Gynecologic Oncology Group. Dactinomycin in the treatment of recurrent or persistent endometrial carcinoma: A Phase II study of the Gynecologic Oncology Group. Gynecol Oncol. 1999 Dec;75(3):473-5. [http://www.gynecologiconcology-online.net/article/S0090-8258(99)95652-4 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/10600310 PubMed]
*[[Panitumumab (Vectibix)]] 6 mg/kg IV once on day 1
+
==Dostarlimab monotherapy {{#subobject:ejg8a3|Regimen=1}}==
'''14-day cycle until POD or resectability or to max 12 cycles'''
+
<div class="toccolours" style="background-color:#eeeeee">
 +
===Regimen {{#subobject:5dnfj9|Variant=1}}===
 +
{| class="wikitable sortable" style="color:white; background-color:#404040"
 +
|<small>'''FDA-recommended dose'''</small>
 +
|-
 +
|}
 +
{| class="wikitable sortable" style="width: 60%; text-align:center;"
 +
!style="width: 33%"|Study
 +
!style="width: 33%"|Years of enrollment
 +
!style="width: 33%"|[[Levels_of_Evidence#Evidence|Evidence]]
 +
|-
 +
|[https://www.ncbi.nlm.nih.gov/pmc/articles/pmc7530821/ Oaknin et al. 2020 (GARNET)]
 +
|2017-2019
 +
| style="background-color:#91cf61" |Phase 1, >20 pts in this cohort (RT)
 +
|-
 +
|}
 +
<div class="toccolours" style="background-color:#b3e2cd">
 +
====Immunotherapy====
 +
*[[Dostarlimab (Jemperli)]] as follows:
 +
**Cycles 1 to 4: 500 mg IV over 30 minutes once on day 1
 +
**Cycle 5 onwards: 1000 mg IV over 30 minutes once on day 1
 +
'''21-day cycle for 4 cycles, then 42-day cycles'''
 
</div></div>
 
</div></div>
 
===References===
 
===References===
#'''VOLFI:''' Modest DP, Martens UM, Riera-Knorrenschild J, Greeve J, Florschütz A, Wessendorf S, Ettrich T, Kanzler S, Nörenberg D, Ricke J, Seidensticker M, Held S, Buechner-Steudel P, Atzpodien J, Heinemann V, Seufferlein T, Tannapfel A, Reinacher-Schick AC, Geissler M. FOLFOXIRI Plus Panitumumab As First-Line Treatment of RAS Wild-Type Metastatic Colorectal Cancer: The Randomized, Open-Label, Phase II VOLFI Study (AIO KRK0109). J Clin Oncol. 2019 Dec 10;37(35):3401-3411. Epub 2019 Oct 14. [https://doi.org/10.1200/JCO.19.01340 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/31609637 PubMed] NCT01328171
+
#'''GARNET:''' Oaknin A, Tinker AV, Gilbert L, Samouëlian V, Mathews C, Brown J, Barretina-Ginesta MP, Moreno V, Gravina A, Abdeddaim C, Banerjee S, Guo W, Danaee H, Im E, Sabatier R. Clinical Activity and Safety of the Anti-Programmed Death 1 Monoclonal Antibody Dostarlimab for Patients With Recurrent or Advanced Mismatch Repair-Deficient Endometrial Cancer: A Nonrandomized Phase 1 Clinical Trial. JAMA Oncol. 2020 Nov 1;6(11):1766-1772. Epub 2020 Oct 1. [https://doi.org/10.1001/jamaoncol.2020.4515 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/pmc7530821/ link to PMC article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/33001143/ PubMed] NCT02715284
=Maintenance after first-line therapy=
+
##'''Update:''' Oaknin A, Gilbert L, Tinker AV, Brown J, Mathews C, Press J, Sabatier R, O'Malley DM, Samouelian V, Boni V, Duska L, Ghamande S, Ghatage P, Kristeleit R, Leath C III, Guo W, Im E, Zildjian S, Han X, Duan T, Veneris J, Pothuri B. Safety and antitumor activity of dostarlimab in patients with advanced or recurrent DNA mismatch repair deficient/microsatellite instability-high (dMMR/MSI-H) or proficient/stable (MMRp/MSS) endometrial cancer: interim results from GARNET-a phase I, single-arm study. J Immunother Cancer. 2022 Jan;10(1):e003777. [https://doi.org/10.1136/jitc-2021-003777 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/pmc8785197/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/35064011/ PubMed]
==Bevacizumab monotherapy {{#subobject:ahag4f|Regimen=1}}==
+
==Doxorubicin monotherapy {{#subobject:e5b103|Regimen=1}}==
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen {{#subobject:a72hg6|Variant=1}}===
+
===Regimen variant #1, 7 cycles {{#subobject:5dn1e9|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
Line 729: Line 824:
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
|-
 
|-
|[https://doi.org/10.1093/annonc/mdv490 Hagman et al. 2015 (Nordic ACT2)]
+
|[https://doi.org/10.1093/annonc/mdg112 Aapro et al. 2003 (EORTC 55872)]
|2010-2012
+
|1988-1994
| style="background-color:#1a9851" |Phase 3 (C)
+
|style="background-color:#1a9851"|Phase 3 (C)
|[[#Erlotinib_.26_Bevacizumab_99|Erlotinib & Bevacizumab]]
+
|[[#Cisplatin_.26_Doxorubicin_2|Cisplatin & Doxorubicin]]
| style="background-color:#ffffbf" |Did not meet primary endpoint of PFS
+
| style="background-color:#fee08b" |Might have inferior OS
 
|-
 
|-
 
|}
 
|}
<div class="toccolours" style="background-color:#fdcdac">
+
''Note: to our knowledge, this regimen was not tested as an experimental arm in an RCT in this context, prior to becoming a standard comparator arm.''
====Biomarker eligibility criteria====
 
*Wild-type KRAS
 
</div>
 
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
====Targeted therapy====
+
====Chemotherapy====
*[[Bevacizumab (Avastin)]] 7.5 mg/kg IV once on day 1
+
*[[Doxorubicin (Adriamycin)]] 60 mg/m<sup>2</sup> IV once on day 1
'''21-day cycles'''
+
'''28-day cycle for up to 7 cycles'''
</div></div>
+
</div></div><br>
===References===
 
#'''Nordic ACT2:''' Hagman H, Frödin JE, Berglund Å, Sundberg J, Vestermark LW, Albertsson M, Fernebro E, Johnsson A. A randomized study of KRAS-guided maintenance therapy with bevacizumab, erlotinib or metronomic capecitabine after first-line induction treatment of metastatic colorectal cancer: the Nordic ACT2 trial. Ann Oncol. 2016 Jan;27(1):140-7. Epub 2015 Oct 19. [https://doi.org/10.1093/annonc/mdv490 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/26483047/ PubMed] NCT01229813
 
==Cetuximab monotherapy {{#subobject:afad4f|Regimen=1}}==
 
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen variant #1, 250 mg/m<sup>2</sup> weekly {{#subobject:a72650|Variant=1}}===
+
===Regimen variant #2, 8 cycles {{#subobject:5d91e9|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
Line 757: Line 846:
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
|-
 
|-
|[https://www.ejcancer.com/article/S0959-8049(18)30938-9 Aranda et al. 2018 (MACRO-2)]
+
|[https://pubmed.ncbi.nlm.nih.gov/369691 Thigpen et al. 1979]
|2010-NR
+
|NR
| style="background-color:#1a9851" |Randomized Phase 2 (E-de-esc)
+
| style="background-color:#91cf61" |Phase 2
|[[#mFOLFOX6_.26_Cetuximab_2|mFOLFOX6 & Cetuximab]]
+
| style="background-color:#d3d3d3" |
| style="background-color:#eeee01" |Non-inferior PFS
+
| style="background-color:#d3d3d3" |
 +
|-
 +
|[https://doi.org/10.1002/1097-0142(19830815)52:4%3C626::AID-CNCR2820520409%3E3.0.CO;2-E Omura et al. 1983 (GOG 21)]
 +
|1973-1979
 +
|style="background-color:#1a9851"|Randomized (C)
 +
|[[#Dacarbazine_.26_Doxorubicin_99|Dacarbazine & Doxorubicin]]
 +
| style="background-color:#ffffbf" |Did not meet primary endpoint of ORR
 
|-
 
|-
|}
+
|[https://doi.org/10.1002/1097-0142(19850415)55:8%3C1648::AID-CNCR2820550806%3E3.0.CO;2-7 Muss et al. 1985 (GOG 42)]
''Note: regimen details are from ClinicalTrials.gov; they were not present in the abstract or the manuscript.''
+
|1979-1982
<div class="toccolours" style="background-color:#fdcdac">
+
|style="background-color:#1a9851"|Phase 3 (C)
====Biomarker eligibility criteria====
+
|[[#Cyclophosphamide_.26_Doxorubicin_.28AC.29_99|Cyclophosphamide & Doxorubicin (AC)]]
*Wild-type KRAS, Wild-type NRAS
+
| style="background-color:#ffffbf" |Did not meet efficacy endpoints
<div class="toccolours" style="background-color:#cbd5e8">
+
|-
</div>
+
|[https://doi.org/10.1200/JCO.1994.12.7.1408 Thigpen et al. 1994 (GOG 48)]
<div class="toccolours" style="background-color:#b3e2cd">
+
|1979-1985
====Preceding treatment====
+
|style="background-color:#1a9851"|Randomized (C)
*[[#mFOLFOX6_.26_Cetuximab_2|mFOLFOX6 & Cetuximab]] x 8
+
|[[#Cyclophosphamide_.26_Doxorubicin_.28AC.29_99|Cyclophosphamide & Doxorubicin (AC)]]
</div>
+
| style="background-color:#ffffbf" |Did not meet efficacy endpoints
<div class="toccolours" style="background-color:#b3e2cd">
+
|-
====Targeted therapy====
+
|[https://doi.org/10.1200/JCO.2004.02.088 Thigpen et al. 2004 (GOG 107)]
*[[Cetuximab (Erbitux)]] 250 mg/m<sup>2</sup> IV once on day 1
+
|NR
'''7-day cycles'''
+
|style="background-color:#1a9851"|Phase 3 (C)
</div></div><br>
+
|[[#Cisplatin_.26_Doxorubicin_2|Cisplatin & Doxorubicin]]
<div class="toccolours" style="background-color:#eeeeee">
+
|style="background-color:#fc8d59"|Seems to have inferior PFS
===Regimen variant #2, 500 mg/m<sup>2</sup> q2wk {{#subobject:3d7e64|Variant=1}}===
 
{| class="wikitable" style="width: 40%; text-align:center;"
 
! style="width: 25%" |Study
 
! style="width: 25%" |[[Levels_of_Evidence#Evidence|Evidence]]
 
 
|-
 
|-
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5885260/ Cremolini et al. 2018 (MACBETH)]
+
|[https://doi.org/10.1056/nejmoa2108330 Makker et al. 2022 (KEYNOTE-775)]
| style="background-color:#91cf61" |Randomized Phase 2
+
|2018-2020
 +
|style="background-color:#1a9851"|Phase 3 (C)
 +
|[[#Lenvatinib_.26_Pembrolizumab|Lenvatinib & Pembrolizumab]]
 +
| style="background-color:#d73027" |Inferior OS
 
|-
 
|-
 
|}
 
|}
''Note: this was a non-comparative study.''
+
''Note: to our knowledge, this regimen was not tested as an experimental arm in an RCT in this context, prior to becoming a standard comparator arm.''
<div class="toccolours" style="background-color:#fdcdac">
 
====Biomarker eligibility criteria====
 
*Wild-type KRAS, Wild-type NRAS
 
<div class="toccolours" style="background-color:#cbd5e8">
 
</div>
 
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
====Preceding treatment====
+
====Chemotherapy====
*[[#mFOLFOXIRI_.26_Cetuximab_.28L-Leucovorin.29|mFOLFOXIRI & Cetuximab]] x 8
+
*[[Doxorubicin (Adriamycin)]] 60 mg/m<sup>2</sup> IV over 60 minutes once on day 1
</div>
+
'''21-day cycle for up to 8 cycles'''
<div class="toccolours" style="background-color:#b3e2cd">
 
====Targeted therapy====
 
*[[Cetuximab (Erbitux)]] 500 mg/m<sup>2</sup> IV once on day 1
 
'''14-day cycles'''
 
 
</div></div>
 
</div></div>
 
===References===
 
===References===
#'''MACBETH:''' Cremolini C, Antoniotti C, Lonardi S, Aprile G, Bergamo F, Masi G, Grande R, Tonini G, Mescoli C, Cardellino GG, Coltelli L, Salvatore L, Corsi DC, Lupi C, Gemma D, Ronzoni M, Dell'Aquila E, Marmorino F, Di Fabio F, Mancini ML, Marcucci L, Fontanini G, Zagonel V, Boni L, Falcone A. Activity and safety of cetuximab plus modified FOLFOXIRI followed by maintenance with cetuximab or bevacizumab for RAS and BRAF wild-type metastatic colorectal cancer: a randomized phase 2 clinical trial. JAMA Oncol. 2018 Apr 1;4(4):529-536. [https://jamanetwork.com/journals/jamaoncology/article-abstract/2672387 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5885260/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/29450468 PubMed] NCT02295930
+
# Thigpen JT, Buchsbaum HJ, Mangan C, Blessing JA; Gynecologic Oncology Group. Phase II trial of adriamycin in the treatment of advanced or recurrent endometrial carcinoma: a Gynecologic Oncology Group study. Cancer Treat Rep. 1979 Jan;63(1):21-7. [https://pubmed.ncbi.nlm.nih.gov/369691 PubMed]
#'''MACRO-2:''' Aranda E, García-Alfonso P, Benavides M, Sánchez Ruiz A, Guillén-Ponce C, Safont MJ, Alcaide J, Gómez A, López R, Manzano JL, Méndez Ureña M, Sastre J, Rivera F, Grávalos C, García T, Martín-Valadés JI, Falcó E, Navalón M, González Flores E, Ma García Tapiador A, Ma López Muñoz A, Barrajón E, Reboredo M, García Teijido P, Viudez A, Cárdenas N, Díaz-Rubio E; Spanish Cooperative Group for the Treatment of Digestive Tumours. First-line mFOLFOX plus cetuximab followed by mFOLFOX plus cetuximab or single-agent cetuximab as maintenance therapy in patients with metastatic colorectal cancer: phase II randomised MACRO2 TTD study. Eur J Cancer. 2018 Sep;101:263-272. Epub 2018 Jul 24. [https://www.ejcancer.com/article/S0959-8049(18)30938-9 link to original article] [https://pubmed.ncbi.nlm.nih.gov/30054049 PubMed] NCT01161316
+
# '''GOG 21:''' Omura GA, Major FJ, Blessing JA, Sedlacek TV, Thigpen JT, Creasman WT, Zaino RJ. A randomized study of adriamycin with and without dimethyl triazenoimidazole carboxamide in advanced uterine sarcomas. Cancer. 1983 Aug 15;52(4):626-32. [https://doi.org/10.1002/1097-0142(19830815)52:4%3C626::AID-CNCR2820520409%3E3.0.CO;2-E link to original article] [https://pubmed.ncbi.nlm.nih.gov/6344983 PubMed]
=Advanced or metastatic disease, second-line=
+
# '''GOG 42:''' Muss HB, Bundy B, DiSaia PJ, Homesley HD, Fowler WC Jr, Creasman W, Yordan E. Treatment of recurrent or advanced uterine sarcoma: a randomized trial of doxorubicin versus doxorubicin and cyclophosphamide (a phase III trial of the Gynecologic Oncology Group). Cancer. 1985 Apr 15;55(8):1648-53. [https://doi.org/10.1002/1097-0142(19850415)55:8%3C1648::AID-CNCR2820550806%3E3.0.CO;2-7 link to original article] [https://pubmed.ncbi.nlm.nih.gov/3884128 PubMed]
==FOLFIRI & Panitumumab {{#subobject:8c0093|Regimen=1}}==
+
# '''GOG 48:''' Thigpen JT, Blessing JA, DiSaia PJ, Yordan E, Carson LF, Evers C. A randomized comparison of doxorubicin alone versus doxorubicin plus cyclophosphamide in the management of advanced or recurrent endometrial carcinoma: a Gynecologic Oncology Group study. J Clin Oncol. 1994 Jul;12(7):1408-14. [https://doi.org/10.1200/JCO.1994.12.7.1408 link to original article] '''contains dosing details in abstract''' [https://pubmed.ncbi.nlm.nih.gov/8021731 PubMed]
FOLFIRI & Panitumumab: '''<u>FOL</u>'''inic acid, '''<u>F</u>'''luorouracil, '''<u>IRI</u>'''notecan, Panitumumab
+
# '''EORTC 55872:''' Aapro MS, van Wijk FH, Bolis G, Chevallier B, van der Burg ME, Poveda A, Freire de Oliveira C, Tumolo S, Scotto di Palumbo V, Piccart M, Franchi M, Zanaboni F, Lacave AJ, Fontanelli R, Favalli G, Zola P, Guastalla JP, Rosso R, Marth C, Nooij M, Presti M, Scarabelli C, Splinter TA, Ploch E, Beex LV, ten Bokkel Huinink W, Forni M, Melpignano M, Blake P, Kerbrat P, Mendiola C, Cervantes A, Goupil A, Harper PG, Madronal C, Namer M, Scarfone G, Stoot JE, Teodorovic I, Coens C, Vergote I, Vermorken JB; [[Study_Groups#EORTC|EORTC]] Gynaecological Cancer Group. Doxorubicin versus doxorubicin and cisplatin in endometrial carcinoma: definitive results of a randomised study (55872) by the EORTC Gynaecological Cancer Group. Ann Oncol. 2003 Mar;14(3):441-8. Erratum in: Ann Oncol. 2003 May;14(5):811. [https://doi.org/10.1093/annonc/mdg112 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/12598351 PubMed]
 +
# '''GOG 107:''' Thigpen JT, Brady MF, Homesley HD, Malfetano J, DuBeshter B, Burger RA, Liao S. Phase III trial of doxorubicin with or without cisplatin in advanced endometrial carcinoma: a Gynecologic Oncology Group study. J Clin Oncol. 2004 Oct 1;22(19):3902-8. [https://doi.org/10.1200/JCO.2004.02.088 link to original article] '''contains dosing details in abstract''' [https://pubmed.ncbi.nlm.nih.gov/15459211 PubMed]
 +
# '''KEYNOTE-775:''' Makker V, Colombo N, Casado Herráez A, Santin AD, Colomba E, Miller DS, Fujiwara K, Pignata S, Baron-Hay S, Ray-Coquard I, Shapira-Frommer R, Ushijima K, Sakata J, Yonemori K, Kim YM, Guerra EM, Sanli UA, McCormack MM, Smith AD, Keefe S, Bird S, Dutta L, Orlowski RJ, Lorusso D; Study 309–KEYNOTE-775 Investigators. Lenvatinib plus Pembrolizumab for Advanced Endometrial Cancer. N Engl J Med. 2022 Feb 3;386(5):437-448. Epub 2022 Jan 19. [https://doi.org/10.1056/nejmoa2108330 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/35045221/ PubMed] NCT03517449
 +
==Ifosfamide monotherapy {{#subobject:b078a0|Regimen=1}}==
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen {{#subobject:ebf6e5|Variant=1}}===
+
===Regimen variant #1, 1200 mg/m<sup>2</sup> (3 days/cycle) {{#subobject:fc7107|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
Line 819: Line 907:
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
|-
 
|-
|[https://doi.org/10.1200/jco.2009.27.6055 Peeters et al. 2010 (20050181)]
+
|[https://doi.org/10.1200/jco.2006.06.4907 Homesley et al. 2007 (GOG 161)]
|2006-2008
+
|1997-2004
| style="background-color:#1a9851" |Phase 3 (E-esc)
+
|style="background-color:#1a9851"|Phase 3 (C)
|[[#FOLFIRI|FOLFIRI]]
+
|[[#Ifosfamide_.26_Paclitaxel|Ifosfamide & Paclitaxel]]
| style="background-color:#91cf60" |Seems to have superior PFS<sup>1</sup><br>Median PFS: 6.7 vs 4.9 mo<br>(HR 0.82, 95% CI 0.69-0.97)
+
|style="background-color:#fc8d59"|Seems to have inferior OS
 
|-
 
|-
 
|}
 
|}
''<sup>1</sup>Reported efficacy is for wild-type KRAS, only, and is based on the 2014 update.''
+
''Note: GOG 161 specifies that PO [[Mesna (Mesnex)]] is to be taken in 3 divided doses, but only lists 2 time points for its use. The timing of the middle dose is estimated based on other references. This dosage is intended for patients with previous radiation.''
<div class="toccolours" style="background-color:#fdcdac">
 
====Biomarker eligibility criteria====
 
*None
 
<div class="toccolours" style="background-color:#fdcdac">
 
</div>
 
<div class="toccolours" style="background-color:#b3e2cd">
 
====Prior treatment criteria====
 
*First-line fluoropyrimidine-based chemotherapy, with progression
 
</div>
 
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
*[[Folinic acid (Leucovorin)]] 400 mg/m<sup>2</sup> IV over 2 hours once on day 1, '''given second, with irinotecan'''
+
*[[Ifosfamide (Ifex)]] 1200 mg/m<sup>2</sup> IV once per day on days 1 to 3
*[[Fluorouracil (5-FU)]] 400 mg/m<sup>2</sup> IV bolus once on day 1, then 2400 mg/m<sup>2</sup> IV continuous infusion over 46 to 48 hours, '''given third''' (total dose per cycle: 2800 mg/m<sup>2</sup>)
+
====Supportive therapy====
*[[Irinotecan (Camptosar)]] 180 mg/m<sup>2</sup> IV over 30 to 90 minutes once on day 1, '''given second, with leucovorin'''
+
*[[Mesna (Mesnex)]] 2000 mg IV over 12 hours once per day on days 1 to 3, starting 15 minutes before [[Ifosfamide (Ifex)]] (total dose per cycle: 6000 mg/m<sup>2</sup>)
====Targeted therapy====
+
**Alternate PO dosing: 1330 mg PO three times per day on days 1 to 3, taken 1 hour before, 4 hours after, and 8 hours after [[Ifosfamide (Ifex)]] (total dose per cycle: 11,970 mg)
*[[Panitumumab (Vectibix)]] 6 mg/kg IV over 60 minutes once on day 1, '''given first'''
+
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day, starting on day 4, to continue until ANC is greater than or equal to 2000/uL
'''14-day cycles'''
+
'''21-day cycle for 8 cycles'''
</div></div>
+
</div></div><br>
===References===
 
#'''20050181:''' Peeters M, Price TJ, Cervantes A, Sobrero AF, Ducreux M, Hotko Y, André T, Chan E, Lordick F, Punt CJ, Strickland AH, Wilson G, Ciuleanu TE, Roman L, Van Cutsem E, Tzekova V, Collins S, Oliner KS, Rong A, Gansert J. Randomized phase III study of panitumumab with fluorouracil, leucovorin, and irinotecan (FOLFIRI) compared with FOLFIRI alone as second-line treatment in patients with metastatic colorectal cancer. J Clin Oncol. 2010 Nov 1;28(31):4706-13. Epub 2010 Oct 4. [https://doi.org/10.1200/jco.2009.27.6055 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/20921462 PubMed] NCT00339183
 
##'''Update:''' Peeters M, Price TJ, Cervantes A, Sobrero AF, Ducreux M, Hotko Y, André T, Chan E, Lordick F, Punt CJ, Strickland AH, Wilson G, Ciuleanu TE, Roman L, Van Cutsem E, Tian Y, Sidhu R. Final results from a randomized phase 3 study of FOLFIRI {+/-} panitumumab for second-line treatment of metastatic colorectal cancer. Ann Oncol. 2014 Jan;25(1):107-16. Erratum in: Ann Oncol. 2014 Mar;25(3):757. [https://doi.org/10.1093/annonc/mdt523 link to original article] [https://pubmed.ncbi.nlm.nih.gov/24356622 PubMed]
 
==Irinotecan monotherapy {{#subobject:d4d4f9|Regimen=1}}==
 
===Example orders===
 
*[[Example orders for Irinotecan (Camptosar) in colon cancer]]
 
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen variant #1, 180 mg/m<sup>2</sup> q2wk {{#subobject:175e25|Variant=1}}===
+
===Regimen variant #2, 1500 mg/m<sup>2</sup> (5 days/cycle) {{#subobject:450cd5|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
Line 860: Line 933:
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
|-
 
|-
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6534840/ Shi et al. 2019 (CRC009)]
+
|[https://www.gynecologiconcology-online.net/article/S0090-8258(00)96001-3/pdf Sutton et al. 2000 (GOG 108)]
|2009-2011
+
|1989-1996
| style="background-color:#1a9851" |Phase 3 (C)
+
|style="background-color:#1a9851"|Phase 3 (C)
|[[#Irinotecan_.26_CMAB009_77|Irinotecan & CMAB009]]
+
|[[#CIM_2|CIM]]
| style="background-color:#d73027" |Inferior PFS50%
+
|style="background-color:#fc8d59"|Seems to have inferior PFS
 
|-
 
|-
 
|}
 
|}
<div class="toccolours" style="background-color:#fdcdac">
 
====Prior treatment criteria====
 
*Exposure to FOLFOX, with progression or discontinuation due to toxicity
 
</div>
 
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
*[[Irinotecan (Camptosar)]] 180 mg/m<sup>2</sup> IV over 90 minutes once on day 1
+
*[[Ifosfamide (Ifex)]] 1500 mg/m<sup>2</sup> IV once per day on days 1 to 5
'''14-day cycles'''
+
====Supportive therapy====
 +
*[[Mesna (Mesnex)]] 1500 mg/m<sup>2</sup> IV once per day on days 1 to 5
 +
'''21-day cycle for 8 cycles'''
 
</div></div><br>
 
</div></div><br>
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen variant #2, 300 mg/m<sup>2</sup> q3wk {{#subobject:190e25|Variant=1}}===
+
===Regimen variant #3, 1600 mg/m<sup>2</sup> (3 days/cycle) {{#subobject:5e6305|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
Line 885: Line 956:
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
|-
 
|-
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3699713/ Seymour et al. 2013 (PICCOLO)]
+
|[https://doi.org/10.1200/jco.2006.06.4907 Homesley et al. 2007 (GOG 161)]
|2006-2008
+
|1997-2004
| style="background-color:#1a9851" |Phase 3 (C)
+
|style="background-color:#1a9851"|Phase 3 (C)
|[[#Irinotecan_.26_Panitumumab_99|Irinotecan & Panitumumab]]
+
|[[#Ifosfamide_.26_Paclitaxel|Ifosfamide & Paclitaxel]]
| style="background-color:#ffffbf" |Did not meet primary endpoint of OS<br>Median OS: 10.9 vs 10.4 mo<br>(HR 0.99, 95% CI 0.81-1.20)
+
|style="background-color:#fc8d59"|Seems to have inferior OS
 
|-
 
|-
 
|}
 
|}
''Note: In some trials, this starting dose was intended for patients who were at least 70 years old, had [[Performance status|ECOG performance status]] 2 or more, or had prior pelvic radiation. Patients in N9841 had not previously received irinotecan or oxaliplatin.''
+
''Note: GOG 161 specifies that PO [[Mesna (Mesnex)]] is to be taken in 3 divided doses, but only lists 2 time points for its use. The timing of the middle dose is estimated based on other references.''
<div class="toccolours" style="background-color:#fdcdac">
 
====Prior treatment criteria====
 
*First-line fluoropyrimidine-based chemotherapy, with progression
 
</div>
 
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
*[[Irinotecan (Camptosar)]] 300 mg/m<sup>2</sup> IV over 90 minutes once on day 1
+
*[[Ifosfamide (Ifex)]] 1600 mg/m<sup>2</sup> IV once per day on days 1 to 3
'''21-day cycles'''
+
**Dosage for patients with previous radiation: 1200 mg/m<sup>2</sup> IV once per day on days 1 to 3
</div></div><br>
+
====Supportive therapy====
 +
*[[Mesna (Mesnex)]] 2000 mg IV over 12 hours once per day on days 1 to 3, starting 15 minutes before [[Ifosfamide (Ifex)]] (total dose per cycle: 6000 mg/m<sup>2</sup>)
 +
**Alternate PO dosing: 1330 mg PO three times per day on days 1 to 3, taken 1 hour before, 4 hours after, and 8 hours after [[Ifosfamide (Ifex)]] (total dose per cycle: 11,970 mg)
 +
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day, starting on day 4, to continue until ANC is greater than or equal to 2000/uL
 +
'''21-day cycle for 8 cycles'''
 +
</div></div>
 +
===References===
 +
# '''GOG 108:''' Sutton G, Brunetto VL, Kilgore L, Soper JT, McGehee R, Olt G, Lentz SS, Sorosky J, Hsiu JG. A phase III trial of ifosfamide with or without cisplatin in carcinosarcoma of the uterus: A Gynecologic Oncology Group study. Gynecol Oncol. 2000 Nov;79(2):147-53. [https://www.gynecologiconcology-online.net/article/S0090-8258(00)96001-3/pdf link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/11063636 PubMed]
 +
# '''GOG 161:''' Homesley HD, Filiaci V, Markman M, Bitterman P, Eaton L, Kilgore LC, Monk BJ, Ueland FR; Gynecologic Oncology Group. Phase III trial of ifosfamide with or without paclitaxel in advanced uterine carcinosarcoma: a Gynecologic Oncology Group study. J Clin Oncol. 2007 Feb 10;25(5):526-31. [https://doi.org/10.1200/jco.2006.06.4907 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/17290061 PubMed] NCT00003128
 +
==Ifosfamide & Paclitaxel {{#subobject:824258|Regimen=1}}==
 +
PI: '''<u>P</u>'''aclitaxel & '''<u>I</u>'''fosfamide
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen variant #3, 350 mg/m<sup>2</sup> q3wk {{#subobject:627110|Variant=1}}===
+
===Regimen {{#subobject:d519c4|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
Line 911: Line 988:
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
|-
 
|-
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3699713/ Seymour et al. 2013 (PICCOLO)]
+
|[https://doi.org/10.1200/jco.2006.06.4907 Homesley et al. 2007 (GOG 161)]
|2006-2008
+
|1997-2004
 +
|style="background-color:#1a9851"|Phase 3 (E-esc)
 +
|[[#Ifosfamide_monotherapy|Ifosfamide]]
 +
|style="background-color:#91cf60"|Seems to have superior OS<br>Median OS: 13.5 vs 8.4 mo<br>(HR 0.69, 95% CI 0.49-0.97)
 +
|-
 +
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8937015/ Powell et al. 2022 (GOG-0261)]
 +
|2009-2014
 
| style="background-color:#1a9851" |Phase 3 (C)
 
| style="background-color:#1a9851" |Phase 3 (C)
|1. [[#Irinotecan_.26_Cyclosporine_99|Irinotecan & Cyclosporine]]<br> 2. [[#Irinotecan_.26_Panitumumab_99|Irinotecan & Panitumumab]]
+
|[[#Carboplatin_.26_Paclitaxel_.28CP.29_2|Carboplatin & Paclitaxel]]
| style="background-color:#ffffbf" |Did not meet primary endpoint of OS<br>Median OS: 10.9 vs 10.4 mo<br>(HR 0.99, 95% CI 0.81-1.20)
+
| style="background-color:#eeee01" |Non-inferior OS
 
|-
 
|-
 
|}
 
|}
<div class="toccolours" style="background-color:#fdcdac">
+
''Note: GOG 161 specifies that PO [[Mesna (Mesnex)]] is to be taken in 3 divided doses, but only lists 2 time points for its use. The timing of the middle dose is estimated based on other references. Treatment was given for 8 cycles in GOG 161.''
====Prior treatment criteria====
 
*First-line fluoropyrimidine-based chemotherapy, with progression
 
</div>
 
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
*[[Irinotecan (Camptosar)]] 350 mg/m<sup>2</sup> IV over 90 minutes once on day 1
+
*[[Ifosfamide (Ifex)]] by the following criteria:
 +
**No previous radiation: 1600 mg/m<sup>2</sup> IV once per day on days 1 to 3
 +
**Previous radiation: 1200 mg/m<sup>2</sup> IV once per day on days 1 to 3
 +
*[[Paclitaxel (Taxol)]] 135 mg/m<sup>2</sup> IV over 3 hours once on day 1
 
====Supportive therapy====
 
====Supportive therapy====
*(varied depending on reference):
+
Per GOG 161:
*"Standard regimens of [[:Category:Emesis_prevention|antiemetics]], [[Atropine (Atropen)]], and intensive [[Loperamide (Imodium)]]," but no prophylactic [[Atropine (Atropen)]] allowed on cycle 1 day 1
+
*[[Mesna (Mesnex)]] 2000 mg IV over 12 hours once per day on days 1 to 3, starting 15 minutes before [[Ifosfamide (Ifex)]] (total dose per cycle: 6000 mg/m<sup>2</sup>)
'''21-day cycles'''
+
**Alternate PO dosing: 1330 mg PO three times per day on days 1 to 3, taken 1 hour before, 4 hours after, and 8 hours after [[Ifosfamide (Ifex)]] (total dose per cycle: 11,970 mg)
 +
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day, starting on day 4, to continue until ANC is greater than or equal to 2000/uL
 +
*[[Dexamethasone (Decadron)]] 20 mg IV or PO for two doses on day 1; 12 and 6 hours prior to [[Paclitaxel (Taxol)]]
 +
*[[Diphenhydramine (Benadryl)]] 50 mg IV once on day 1; 30 minutes prior to [[Paclitaxel (Taxol)]]
 +
*One of the following H2 blockers:
 +
**[[Cimetidine (Tagamet)]] 300 mg IV once on day 1; 30 minutes prior to [[Paclitaxel (Taxol)]]
 +
**[[Ranitidine (Zantac)]] 50 mg IV once on day 1; 30 minutes prior to [[Paclitaxel (Taxol)]]
 +
'''21-day cycle for 6 to 10 cycles'''
 
</div></div>
 
</div></div>
 
===References===
 
===References===
#'''PICCOLO:''' Seymour MT, Brown SR, Middleton G, Maughan T, Richman S, Gwyther S, Lowe C, Seligmann JF, Wadsley J, Maisey N, Chau I, Hill M, Dawson L, Falk S, O'Callaghan A, Benstead K, Chambers P, Oliver A, Marshall H, Napp V, Quirke P. Panitumumab and irinotecan versus irinotecan alone for patients with KRAS wild-type, fluorouracil-resistant advanced colorectal cancer (PICCOLO): a prospectively stratified randomised trial. Lancet Oncol. 2013 Jul;14(8):749-59. Epub 2013 May 29. [https://dx.doi.org/10.1016%2FS1470-2045(13)70163-3 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3699713/ link to PMC article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/23725851 PubMed] NCT00389870
+
# '''GOG 161:''' Homesley HD, Filiaci V, Markman M, Bitterman P, Eaton L, Kilgore LC, Monk BJ, Ueland FR; Gynecologic Oncology Group. Phase III trial of ifosfamide with or without paclitaxel in advanced uterine carcinosarcoma: a Gynecologic Oncology Group study. J Clin Oncol. 2007 Feb 10;25(5):526-31. [https://doi.org/10.1200/jco.2006.06.4907 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/17290061 PubMed] NCT00003128
#'''CRC009:''' Shi Y, Li J, Xu J, Sun Y, Wang L, Cheng Y, Liu W, Sun G, Chen Y, Bai L, Zhang Y, He X, Luo Y, Wang Z, Liu Y, Yao Q, Li Y, Qin S, Hu X, Bi F, Zheng R, Ouyang X. CMAB009 plus irinotecan versus irinotecan-only as second-line treatment after fluoropyrimidine and oxaliplatin failure in KRAS wild-type metastatic colorectal cancer patients: promising findings from a prospective, open-label, randomized, phase III trial. Cancer Commun (Lond). 2019 May 24;39(1):28. [https://dx.doi.org/10.1186/s40880-019-0374-8 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6534840/ link to PMC article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/31126331 PubMed] NCT01550055
+
# '''GOG-0261:''' Powell MA, Filiaci VL, Hensley ML, Huang HQ, Moore KN, Tewari KS, Copeland LJ, Secord AA, Mutch DG, Santin A, Warshal DP, Spirtos NM, DiSilvestro PA, Ioffe OB, Miller DS. Randomized Phase III Trial of Paclitaxel and Carboplatin Versus Paclitaxel and Ifosfamide in Patients With Carcinosarcoma of the Uterus or Ovary: An NRG Oncology Trial. J Clin Oncol. 2022 Mar 20;40(9):968-977. Epub 2022 Jan 10. [https://doi.org/10.1200/jco.21.02050 link to original article] '''contains dosing details in manuscript''' [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8937015/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/35007153/ PubMed] NCT00954174
==Irinotecan & Cetuximab {{#subobject:c912ee|Regimen=1}}==
+
==Lenvatinib & Pembrolizumab {{#subobject:cffdf6|Regimen=1}}==
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen {{#subobject:b7315f|Variant=1}}===
+
===Regimen {{#subobject:a27gua|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
Line 943: Line 1,033:
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
|-
 
|-
|[https://doi.org/10.1200/jco.2007.13.1193 Sobrero et al. 2008 (EPIC)]
+
|[https://doi.org/10.1016/S1470-2045(19)30020-8 Makker et al. 2019 (KEYNOTE-146)]
|2003-2006
+
|2015-2017
| style="background-color:#1a9851" |Phase 3 (E-esc)
+
|style="background-color:#91cf61"|Phase 2 (RT)
|[[Colon_cancer#Irinotecan_monotherapy_2|Irinotecan]]
+
| style="background-color:#d3d3d3" |
| style="background-color:#ffffbf" |Did not meet primary endpoint of OS
+
| style="background-color:#d3d3d3" |
 +
|-
 +
|[https://doi.org/10.1056/nejmoa2108330 Makker et al. 2022 (KEYNOTE-775)]
 +
|2018-2020
 +
|style="background-color:#1a9851"|Phase 3 (E-RT-switch-ooc)
 +
|1. [[#Doxorubicin_monotherapy|Doxorubicin]]<br>2. [[#Paclitaxel_monotherapy|Paclitaxel]]
 +
| style="background-color:#1a9850" |Superior OS<sup>1</sup><br>Median OS: 18.3 vs 11.4 mo<br>(HR 0.62, 95% CI 0.51-0.75)
 
|-
 
|-
 
|}
 
|}
<div class="toccolours" style="background-color:#fdcdac">
+
''<sup>1</sup>Reported efficacy is for the overall population.''
====Prior treatment criteria====
 
*First-line fluoropyrimidine and oxaliplatin treatment, with progression or discontinuation due to toxicity
 
</div>
 
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
====Chemotherapy====
 
*[[Irinotecan (Camptosar)]] 350 mg/m<sup>2</sup> IV over 90 minutes once on day 1
 
**If aged 70 years old or more, [[Performance status|ECOG performance status]] 2 or more, or prior pelvic radiation: 300 mg/m<sup>2</sup> IV over 90 minutes once on day 1
 
 
====Targeted therapy====
 
====Targeted therapy====
*[[Cetuximab (Erbitux)]] as follows:
+
*[[Lenvatinib (Lenvima)]] 20 mg PO once per day
**Cycle 1: 400 mg/m<sup>2</sup> IV over 2 hours once on day 1, then 250 mg/m<sup>2</sup> IV over 60 minutes once per day on days 8 & 15
+
====Immunotherapy====
**Cycle 2 onwards: 250 mg/m<sup>2</sup> IV over 60 minutes once per day on days 1, 8, 15
+
*[[Pembrolizumab (Keytruda)]] as follows:
====Supportive therapy====
+
**Cycle 1 up to 35: 200 mg IV over 30 minutes once on day 1
*[[:Category:Antihistamines|Antihistamine]] prior to at least the first infusion of [[Cetuximab (Erbitux)]]
 
 
'''21-day cycles'''
 
'''21-day cycles'''
 
</div></div>
 
</div></div>
 
===References===
 
===References===
<!-- Presented in part at the 41st Annual Meeting of the American Society of Clinical Oncology, Orlando, FL, June 2005; the 42nd Annual Meeting of the American Society of Clinical Oncology, Atlanta, GA, June 2006; safety and efficacy results from this study were presented at the Annual Meeting of the American Association for Cancer Research, April 14-18, 2007, Los Angeles, CA; and the quality of life results from this study were presented at the 43rd Annual Meeting of the American Society of Clinical Oncology, Chicago, IL, June 2007. -->
+
# '''KEYNOTE-146:''' Makker V, Rasco D, Vogelzang NJ, Brose MS, Cohn AL, Mier J, Di Simone C, Hyman DM, Stepan DE, Dutcus CE, Schmidt EV, Guo M, Sachdev P, Shumaker R, Aghajanian C, Taylor M. Lenvatinib plus pembrolizumab in patients with advanced endometrial cancer: an interim analysis of a multicentre, open-label, single-arm, phase 2 trial. Lancet Oncol. 2019 May;20(5):711-718. Epub 2019 Mar 25. [https://doi.org/10.1016/S1470-2045(19)30020-8 link to original article] '''contains dosing details in abstract''' [https://pubmed.ncbi.nlm.nih.gov/30922731 PubMed] NCT02501096
#'''EPIC:''' Sobrero AF, Maurel J, Fehrenbacher L, Scheithauer W, Abubakr YA, Lutz MP, Vega-Villegas ME, Eng C, Steinhauer EU, Prausova J, Lenz HJ, Borg C, Middleton G, Kröning H, Luppi G, Kisker O, Zubel A, Langer C, Kopit J, Burris HA 3rd. EPIC: phase III trial of cetuximab plus irinotecan after fluoropyrimidine and oxaliplatin failure in patients with metastatic colorectal cancer. J Clin Oncol. 2008 May 10;26(14):2311-9. Epub 2008 Apr 7. [https://doi.org/10.1200/jco.2007.13.1193 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/18390971 PubMed] NCT00063141
+
##'''Update:''' Makker V, Taylor MH, Aghajanian C, Oaknin A, Mier J, Cohn AL, Romeo M, Bratos R, Brose MS, DiSimone C, Messing M, Stepan DE, Dutcus CE, Wu J, Schmidt EV, Orlowski R, Sachdev P, Shumaker R, Casado Herraez A. Lenvatinib Plus Pembrolizumab in Patients With Advanced Endometrial Cancer. J Clin Oncol. 2020 Sep 10;38(26):2981-2992. Epub 2020 Mar 13. [https://doi.org/10.1200/jco.19.02627 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/pmc7479759/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/32167863/ PubMed]
=Advanced or metastatic disease, subsequent lines of therapy=
+
# '''KEYNOTE-775:''' Makker V, Colombo N, Casado Herráez A, Santin AD, Colomba E, Miller DS, Fujiwara K, Pignata S, Baron-Hay S, Ray-Coquard I, Shapira-Frommer R, Ushijima K, Sakata J, Yonemori K, Kim YM, Guerra EM, Sanli UA, McCormack MM, Smith AD, Keefe S, Bird S, Dutta L, Orlowski RJ, Lorusso D; Study 309–KEYNOTE-775 Investigators. Lenvatinib plus Pembrolizumab for Advanced Endometrial Cancer. N Engl J Med. 2022 Feb 3;386(5):437-448. Epub 2022 Jan 19. [https://doi.org/10.1056/nejmoa2108330 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/35045221/ PubMed] NCT03517449
==Cetuximab monotherapy {{#subobject:a41ec2|Regimen=1}}==
+
==Paclitaxel monotherapy {{#subobject:ceedf6|Regimen=1}}==
===Example orders===
 
*[[Example orders for Cetuximab (Erbitux) in colon cancer]]
 
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen variant #1, weekly {{#subobject:e4f241|Variant=1}}===
+
===Regimen variant #1, 80 mg/m<sup>2</sup> {{#subobject:f1676a|Variant=1}}===
{| class="wikitable" style="color:white; background-color:#404040"
+
{| class="wikitable sortable" style="width: 100%; text-align:center;"
|<small>'''FDA-recommended dose'''</small>
+
!style="width: 20%"|Study
 +
!style="width: 20%"|Years of enrollment
 +
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 +
!style="width: 20%"|Comparator
 +
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 +
|-
 +
|[https://doi.org/10.1056/nejmoa2108330 Makker et al. 2022 (KEYNOTE-775)]
 +
|2018-2020
 +
|style="background-color:#1a9851"|Phase 3 (C)
 +
|[[#Lenvatinib_.26_Pembrolizumab|Lenvatinib & Pembrolizumab]]
 +
| style="background-color:#d73027" |Inferior OS
 
|-
 
|-
 
|}
 
|}
 +
''Note: to our knowledge, this regimen was not tested as an experimental arm in an RCT in this context, prior to becoming a standard comparator arm.''
 +
<div class="toccolours" style="background-color:#b3e2cd">
 +
====Chemotherapy====
 +
*[[Paclitaxel (Taxol)]] 80 mg/m<sup>2</sup> IV over 60 minutes once per day on days 1, 8, 15
 +
'''28-day cycles'''
 +
</div></div><br>
 +
<div class="toccolours" style="background-color:#eeeeee">
 +
===Regimen variant #2, 175 mg/m<sup>2</sup> {{#subobject:f1656b|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
Line 986: Line 1,091:
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
|-
 
|-
|[https://doi.org/10.1200/JCO.2004.10.182 Saltz et al. 2004]
+
|[https://doi.org/10.1093/oxfordjournals.annonc.a010768 Lissoni et al. 1996]
|2001
+
|1993-1995
| style="background-color:#91cf61" |Phase 2 (RT)
+
|style="background-color:#91cf61"|Phase 2
 
| style="background-color:#d3d3d3" |
 
| style="background-color:#d3d3d3" |
 
| style="background-color:#d3d3d3" |
 
| style="background-color:#d3d3d3" |
 
|-
 
|-
|[https://doi.org/10.1056/NEJMoa033025 Cunningham et al. 2004 (BOND)]
+
|[http://www.gynecologiconcology-online.net/article/S0090-8258(02)00068-9 Lincoln et al. 2003]
|2001-2002
+
|1994-1996
| style="background-color:#1a9851" |Phase 3 (C)
+
|style="background-color:#91cf61"|Phase 2
|[[#Irinotecan_.26_Cetuximab_2|Irinotecan & Cetuximab]]
 
| style="background-color:#d73027" |Inferior TTP
 
|-
 
|[https://doi.org/10.1200/jco.2006.06.7595 Lenz et al. 2006 (SALVAGE)]
 
|NR
 
| style="background-color:#91cf61" |Phase 2
 
 
| style="background-color:#d3d3d3" |
 
| style="background-color:#d3d3d3" |
 
| style="background-color:#d3d3d3" |
 
| style="background-color:#d3d3d3" |
 
|-
 
|-
|[https://doi.org/10.1056/NEJMoa071834 Jonker et al. 2007 (NCIC-CTG CO.17)]
+
|[https://www.gynecologiconcology-online.net/article/S0090-8258(15)00855-0 McMeekin et al. 2015 (IXAMPLE2)]
|2003-2005
+
|2009-2012
| style="background-color:#1a9851" |Phase 3 (E-RT-esc)
 
|[[Colon_cancer_-_null_regimens#Best_supportive_care_2|Best supportive care]]
 
| style="background-color:#1a9850" |Superior OS<br>Median OS: 6.1 vs 4.6 mo<br>(HR 0.77, 95% CI 0.64-0.92)
 
|-
 
|[https://doi.org/10.1200/JCO.2012.46.0543 Siu et al. 2013 (NCIC-CTG/AGITG CO.20)]
 
|2008-2011
 
| style="background-color:#1a9851" |Phase 3 (C)
 
|[[#Brivanib_.26_Cetuximab_77|Brivanib & Cetuximab]]
 
| style="background-color:#ffffbf" |Did not meet primary endpoint of OS
 
|-
 
|[https://doi.org/10.1016/S1470-2045(14)70118-4 Price et al. 2014 (ASPECCT)]
 
|2010-2012
 
 
| style="background-color:#1a9851" |Phase 3 (C)
 
| style="background-color:#1a9851" |Phase 3 (C)
|[[#Panitumumab_monotherapy|Panitumumab]]
+
|[[#Ixabepilone_monotherapy_99|Ixabepilone]]
| style="background-color:#eeee01" |Non-inferior OS
+
| style="background-color:#91cf60" |Seems to have superior OS
 
|-
 
|-
 
|}
 
|}
<div class="toccolours" style="background-color:#fdcdac">
+
''Note: in Lincoln et al. 2003, this was the dosage for patients with previous pelvic radiation.''
====Prior treatment criteria====
 
*Saltz et al. 2004: Exposure to irinotecan-containing therapy, with clinical failure
 
*BOND: Exposure to irinotecan-containing therapy, with progression
 
*SALVAGE: Exposure to irinotecan, oxaliplatin, and a fluoropyrimidine
 
*NCIC-CTG CO.17: Exposure to irinotecan, oxaliplatin, and a fluoropyrimidine or contraindication to these drugs
 
*NCIC-CTG/AGITG CO.20: Exposure to a fluoropyrimidine and exposure to irinotecan and oxaliplatin or contraindication to these drugs
 
</div>
 
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
====Targeted therapy====
+
====Chemotherapy====
*[[Cetuximab (Erbitux)]] as follows:
+
*[[Paclitaxel (Taxol)]] 175 mg/m<sup>2</sup> IV over 3 hours once on day 1
**Cycle 1: 400 mg/m<sup>2</sup> IV over 2 hours once on day 1, then 250 mg/m<sup>2</sup> IV over 60 minutes once per day on days 8, 15, 22
 
**Cycle 2 onwards: 250 mg/m<sup>2</sup> IV over 60 minutes once per day on days 1, 8, 15, 22
 
 
====Supportive therapy====
 
====Supportive therapy====
*Varies depending on reference
+
*[[Hydrocortisone (Cortef)]] 250 mg IV once on day 1; 60 minutes prior to [[Paclitaxel (Taxol)]]
*[[:Category:Antihistamines|Antihistamine]] (such as [[Diphenhydramine (Benadryl)]] 50 mg IV) prior to at least the first infusion of [[Cetuximab (Erbitux)]]
+
*[[Chlorpheniramine (Chlor-Trimeton)]] 10 mg IM once on day 1; 60 minutes prior to [[Paclitaxel (Taxol)]]
'''28-day cycles'''
+
*[[Cimetidine (Tagamet)]] 300 mg IV once on day 1; 60 minutes prior to [[Paclitaxel (Taxol)]]
 +
'''21-day cycles'''
 
</div></div><br>
 
</div></div><br>
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen variant #2, bi-weekly {{#subobject:315dde|Variant=1}}===
+
===Regimen variant #3, 200 mg/m<sup>2</sup> {{#subobject:a2c4fa|Variant=1}}===
{| class="wikitable" style="width: 40%; text-align:center;"  
+
{| class="wikitable sortable" style="width: 60%; text-align:center;"  
! style="width: 25%" |Study
+
!style="width: 33%"|Study
! style="width: 25%" |[[Levels_of_Evidence#Evidence|Evidence]]
+
!style="width: 33%"|Years of enrollment
 +
!style="width: 33%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
|-
 
|-
|[https://doi.org/10.1093/annonc/mdp549 Tabernero et al. 2009]
+
|[http://www.gynecologiconcology-online.net/article/S0090-8258(96)90227-9 Ball et al. 1996]
| style="background-color:#ffffbe" |Phase 1
+
|NR in abstract
 +
|style="background-color:#91cf61"|Phase 2
 
|-
 
|-
|}
+
|[http://www.gynecologiconcology-online.net/article/S0090-8258(02)00068-9 Lincoln et al. 2003]
''Note: no primary reference could be found for this exact dosing in monotherapy; in the phase I trial it is described as "the most convenient and feasible dose".''
+
|1994-1996
<div class="toccolours" style="background-color:#b3e2cd">
+
|style="background-color:#91cf61"|Phase 2
====Targeted therapy====
 
*[[Cetuximab (Erbitux)]] 500 mg/m<sup>2</sup> IV over 2 hours once on day 1
 
**If tolerated, subsequent doses can be given over 1 hour
 
====Supportive therapy====
 
*[[:Category:Antihistamines|Antihistamine]] prior to [[Cetuximab (Erbitux)]]
 
'''14-day cycles'''
 
</div></div>
 
===References===
 
#Saltz LB, Meropol NJ, Loehrer PJ Sr, Needle MN, Kopit J, Mayer RJ. Phase II trial of cetuximab in patients with refractory colorectal cancer that expresses the epidermal growth factor receptor. J Clin Oncol. 2004 Apr 1;22(7):1201-8. Epub 2004 Mar 1. [https://doi.org/10.1200/JCO.2004.10.182 link to original article] [https://pubmed.ncbi.nlm.nih.gov/14993230 PubMed]
 
#'''BOND:''' Cunningham D, Humblet Y, Siena S, Khayat D, Bleiberg H, Santoro A, Bets D, Mueser M, Harstrick A, Verslype C, Chau I, Van Cutsem E. Cetuximab monotherapy and cetuximab plus irinotecan in irinotecan-refractory metastatic colorectal cancer. N Engl J Med. 2004 Jul 22;351(4):337-45. [https://doi.org/10.1056/NEJMoa033025 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/15269313 PubMed]
 
#'''SALVAGE:''' Lenz HJ, Van Cutsem E, Khambata-Ford S, Mayer RJ, Gold P, Stella P, Mirtsching B, Cohn AL, Pippas AW, Azarnia N, Tsuchihashi Z, Mauro DJ, Rowinsky EK. Multicenter phase II and translational study of cetuximab in metastatic colorectal carcinoma refractory to irinotecan, oxaliplatin, and fluoropyrimidines. J Clin Oncol. 2006 Oct 20;24(30):4914-21. [https://doi.org/10.1200/jco.2006.06.7595 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/17050875 PubMed]
 
<!-- # Bristol-Myers Squibb and ImClone. A Phase III Randomized Study of Cetuximab (Erbitux, C225) and Best Supportive Care Versus Best Supportive Care in Patients with Pretreated Metastatic Epidermal Growth Factor Receptor (EGFR)-Positive Colorectal Carcinoma. Final Clinical Study Report for CA225025. 2007 Mar 5. [http://ctr.bms.com/pdf//CA225025.pdf link to original report] '''contains dosing details in manuscript''' -->
 
#'''NCIC-CTG CO.17:''' Jonker DJ, O'Callaghan CJ, Karapetis CS, Zalcberg JR, Tu D, Au HJ, Berry SR, Krahn M, Price T, Simes RJ, Tebbutt NC, van Hazel G, Wierzbicki R, Langer C, Moore MJ. Cetuximab for the treatment of colorectal cancer. N Engl J Med. 2007 Nov 15;357(20):2040-8. [https://doi.org/10.1056/NEJMoa071834 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/18003960 PubMed] NCT00079066
 
##'''Subgroup analysis:''' Karapetis CS, Khambata-Ford S, Jonker DJ, O'Callaghan CJ, Tu D, Tebbutt NC, Simes RJ, Chalchal H, Shapiro JD, Robitaille S, Price TJ, Shepherd L, Au HJ, Langer C, Moore MJ, Zalcberg JR. K-ras mutations and benefit from cetuximab in advanced colorectal cancer. N Engl J Med. 2008 Oct 23;359(17):1757-65. [https://doi.org/10.1056/NEJMoa0804385 link to original article] [https://pubmed.ncbi.nlm.nih.gov/18946061 PubMed]
 
##'''Subgroup analysis:''' Asmis TR, Powell E, Karapetis CS, Jonker DJ, Tu D, Jeffery M, Pavlakis N, Gibbs P, Zhu L, Dueck DA, Whittom R, Langer C, O'Callaghan CJ. Comorbidity, age and overall survival in cetuximab-treated patients with advanced colorectal cancer (ACRC)--results from NCIC-CTG CO.17: a phase III trial of cetuximab versus best supportive care. Ann Oncol. 2011 Jan;22(1):118-26. Epub 2010 Jul 5. [https://doi.org/10.1093/annonc/mdq309 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/20603436 PubMed]
 
#'''Phase I:''' Tabernero J, Ciardiello F, Rivera F, Rodriguez-Braun E, Ramos FJ, Martinelli E, Vega-Villegas ME, Roselló S, Liebscher S, Kisker O, Macarulla T, Baselga J, Cervantes A. Cetuximab administered once every second week to patients with metastatic colorectal cancer: a two-part pharmacokinetic/pharmacodynamic phase I dose-escalation study. Ann Oncol. 2010 Jul;21(7):1537-45. Epub 2009 Nov 25. [https://doi.org/10.1093/annonc/mdp549 link to original article] [https://pubmed.ncbi.nlm.nih.gov/19940007 PubMed]
 
#'''NCIC-CTG/AGITG CO.20:''' Siu LL, Shapiro JD, Jonker DJ, Karapetis CS, Zalcberg JR, Simes J, Couture F, Moore MJ, Price TJ, Siddiqui J, Nott LM, Charpentier D, Liauw W, Sawyer MB, Jefford M, Magoski NM, Haydon A, Walters I, Ringash J, Tu D, O'Callaghan CJ. Phase III randomized, placebo-controlled study of cetuximab plus brivanib alaninate versus cetuximab plus placebo in patients with metastatic, chemotherapy-refractory, wild-type K-RAS colorectal carcinoma: the NCIC Clinical Trials Group and AGITG CO.20 Trial. J Clin Oncol. 2013 Jul 1;31(19):2477-84. Epub 2013 May 20. [https://doi.org/10.1200/JCO.2012.46.0543 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/23690424 PubMed] NCT00640471
 
#'''ASPECCT:''' Price TJ, Peeters M, Kim TW, Li J, Cascinu S, Ruff P, Suresh AS, Thomas A, Tjulandin S, Zhang K, Murugappan S, Sidhu R. Panitumumab versus cetuximab in patients with chemotherapy-refractory wild-type KRAS exon 2 metastatic colorectal cancer (ASPECCT): a randomised, multicentre, open-label, non-inferiority phase 3 study. Lancet Oncol. 2014 May;15(6):569-79. Epub 2014 Apr 14. [https://doi.org/10.1016/S1470-2045(14)70118-4 link to original article] [https://pubmed.ncbi.nlm.nih.gov/24739896 PubMed] NCT01001377
 
##'''Update:''' Price T, Kim TW, Li J, Cascinu S, Ruff P, Suresh AS, Thomas A, Tjulandin S, Guan X, Peeters M. Final results and outcomes by prior bevacizumab exposure, skin toxicity, and hypomagnesaemia from ASPECCT: randomized phase 3 non-inferiority study of panitumumab versus cetuximab in chemorefractory wild-type KRAS exon 2 metastatic colorectal cancer. Eur J Cancer. 2016 Nov;68:51-59. Epub 2016 Oct 5. [https://doi.org/10.1016/j.ejca.2016.08.010 link to original article] [https://pubmed.ncbi.nlm.nih.gov/27716478 PubMed]
 
==Irinotecan & Cetuximab {{#subobject:5d7e80|Regimen=1}}==
 
<div class="toccolours" style="background-color:#eeeeee">
 
===Regimen variant #1, 125/250, irinotecan 2 weeks on, 1 week off {{#subobject:e734bb|Variant=1}}===
 
{| class="wikitable" style="color:white; background-color:#404040"
 
|<small>'''FDA-recommended dose'''</small>
 
 
|-
 
|-
 
|}
 
|}
''Note: In contrast to BOND, some guidelines list irinotecan as being given on days 1 & 8 of a 21-day cycle. No primary reference could be found for this. Note also that the FDA-recommended dosing is for the cetuximab component; no comment is made about irinotecan dosing.''
+
''Note: in Ball et al. 1996, this was the dosage for patients with previous pelvic radiation.''
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
*[[Irinotecan (Camptosar)]] 125 mg/m<sup>2</sup> IV over 90 minutes once per day on days 1 & 8
+
*[[Paclitaxel (Taxol)]] 200 mg/m<sup>2</sup> IV over 3 hours once on day 1
====Targeted therapy====
+
**Ball et al. 1996 gave as a 24 hour continuous infusion
*[[Cetuximab (Erbitux)]] as follows:
+
**Dose can be changed to 135 or 110 mg/m<sup>2</sup> depending on toxicity
**Cycle 1: 400 mg/m<sup>2</sup> IV over 2 hours once on day 1, then 250 mg/m<sup>2</sup> IV over 60 minutes once per day on days 8 & 15
 
**Cycle 2 onwards: 250 mg/m<sup>2</sup> IV over 60 minutes once per day on days 1, 8, 15
 
 
====Supportive therapy====
 
====Supportive therapy====
*[[:Category:Antihistamines|Antihistamine]] prior to at least the first infusion of [[Cetuximab (Erbitux)]]
+
*[[Dexamethasone (Decadron)]] 20 mg IV or PO for 2 doses on day 1; 12 and 6 hours prior to [[Paclitaxel (Taxol)]]
 +
*[[Diphenhydramine (Benadryl)]] 50 mg IV or PO once on day 1; 30 minutes prior to [[Paclitaxel (Taxol)]]
 +
*[[Cimetidine (Tagamet)]] 300 mg IV once on day 1; 30 minutes prior to [[Paclitaxel (Taxol)]]
 
'''21-day cycles'''
 
'''21-day cycles'''
 
</div></div><br>
 
</div></div><br>
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen variant #2, 125/250, irinotecan 4 weeks on, 2 weeks off {{#subobject:a4d073|Variant=1}}===
+
===Regimen variant #4, 250 mg/m<sup>2</sup> {{#subobject:68d2e|Variant=1}}===
{| class="wikitable" style="color:white; background-color:#404040"
+
{| class="wikitable" style="width: 40%; text-align:center;"  
|<small>'''FDA-recommended dose'''</small>
+
!style="width: 25%"|Study
|-
+
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
|}
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Years of enrollment
 
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 20%"|Comparator
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
 
|-
 
|-
|[https://doi.org/10.1056/NEJMoa033025 Cunningham et al. 2004 (BOND)]
+
|[http://www.gynecologiconcology-online.net/article/S0090-8258(96)90227-9 Ball et al. 1996]
|2001-2002
+
|style="background-color:#91cf61"|Phase 2
| style="background-color:#1a9851" |Phase 3 (E-RT-esc)
 
|[[#Cetuximab_monotherapy_2|Cetuximab]]
 
| style="background-color:#1a9850" |Superior TTP
 
 
|-
 
|-
 
|}
 
|}
''Note that the FDA-recommended dosing is for the cetuximab component; no comment is made about irinotecan dosing.''
 
<div class="toccolours" style="background-color:#fdcdac">
 
====Prior treatment criteria====
 
*BOND: Exposure to irinotecan-containing therapy, with progression
 
</div>
 
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
*[[Irinotecan (Camptosar)]] 125 mg/m<sup>2</sup> IV over 90 minutes once per day on days 1, 8, 15, 22
+
*[[Paclitaxel (Taxol)]] 250 mg/m<sup>2</sup> IV continuous infusion over 24 hours, started on day 1
====Targeted therapy====
+
**Dosage for patients with previous pelvic radiation: 200 mg/m<sup>2</sup> IV continuous infusion over 24 hours, started on day 1
*[[Cetuximab (Erbitux)]] as follows:
+
**Dose can be changed to 200, 170, 135, 110 mg/m<sup>2</sup> depending on toxicity
**Cycle 1: 400 mg/m<sup>2</sup> IV over 2 hours once on day 1, then 250 mg/m<sup>2</sup> IV over 60 minutes once per day on days 8, 15, 22, 29, 36
 
**Cycle 2 onwards: 250 mg/m<sup>2</sup> IV over 60 minutes once per day on days 1, 8, 15, 22, 29, 36
 
 
====Supportive therapy====
 
====Supportive therapy====
*[[:Category:Antihistamines|Antihistamine]] prior to at least the first infusion of [[Cetuximab (Erbitux)]]
+
*[[Dexamethasone (Decadron)]] 20 mg IV or PO for 2 doses on day 1; 12 and 6 hours prior to [[Paclitaxel (Taxol)]]
'''42-day cycles'''
+
*[[Diphenhydramine (Benadryl)]] 50 mg IV or PO once on day 1; 30 minutes prior to [[Paclitaxel (Taxol)]]
</div></div><br>
+
*[[Cimetidine (Tagamet)]] 300 mg IV once on day 1; 30 minutes prior to [[Paclitaxel (Taxol)]]
 +
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day, starting on day 3, 24 hours after [[Paclitaxel (Taxol)]], continued for at least 12 days or until two successive total leukocyte counts are 10,000 or greater, whichever comes last
 +
'''21-day cycles'''
 +
</div></div>
 +
===References===
 +
# Ball HG, Blessing JA, Lentz SS, Mutch DG; Gynecologic Oncology Group. A phase II trial of paclitaxel in patients with advanced or recurrent adenocarcinoma of the endometrium: a Gynecologic Oncology Group study. Gynecol Oncol. 1996 Aug;62(2):278-81. [http://www.gynecologiconcology-online.net/article/S0090-8258(96)90227-9 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/8751561 PubMed]
 +
# Lissoni A, Zanetta G, Losa G, Gabriele A, Parma G, Mangioni C. Phase II study of paclitaxel as salvage treatment in advanced endometrial cancer. Ann Oncol. 1996 Oct;7(8):861-3. [https://doi.org/10.1093/oxfordjournals.annonc.a010768 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/8922203 PubMed]
 +
# Lincoln S, Blessing JA, Lee RB, Rocereto TF; Gynecologic Oncology Group. Activity of paclitaxel as second-line chemotherapy in endometrial carcinoma: a Gynecologic Oncology Group study. Gynecol Oncol. 2003 Mar;88(3):277-81. [http://www.gynecologiconcology-online.net/article/S0090-8258(02)00068-9 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/12648575 PubMed]
 +
# '''IXAMPLE2:''' McMeekin S, Dizon D, Barter J, Scambia G, Manzyuk L, Lisyanskaya A, Oaknin A, Ringuette S, Mukhopadhyay P, Rosenberg J, Vergote I. Phase III randomized trial of second-line ixabepilone versus paclitaxel or doxorubicin in women with advanced endometrial cancer. Gynecol Oncol. 2015 Jul;138(1):18-23. Epub 2015 Apr 26. [https://www.gynecologiconcology-online.net/article/S0090-8258(15)00855-0 link to original article] '''contains dosing details in abstract''' [https://pubmed.ncbi.nlm.nih.gov/25925990 PubMed] NCT00883116
 +
# '''KEYNOTE-775:''' Makker V, Colombo N, Casado Herráez A, Santin AD, Colomba E, Miller DS, Fujiwara K, Pignata S, Baron-Hay S, Ray-Coquard I, Shapira-Frommer R, Ushijima K, Sakata J, Yonemori K, Kim YM, Guerra EM, Sanli UA, McCormack MM, Smith AD, Keefe S, Bird S, Dutta L, Orlowski RJ, Lorusso D; Study 309–KEYNOTE-775 Investigators. Lenvatinib plus Pembrolizumab for Advanced Endometrial Cancer. N Engl J Med. 2022 Feb 3;386(5):437-448. Epub 2022 Jan 19. [https://doi.org/10.1056/nejmoa2108330 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/35045221/ PubMed] NCT03517449
 +
==Pembrolizumab monotherapy {{#subobject:e0d17a|Regimen=1}}==
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen variant #3, 150/500, bi-weekly {{#subobject:c0c538|Variant=1}}===
+
===Regimen variant #1, bi-weekly {{#subobject:87f9c7|Variant=1}}===
 
{| class="wikitable sortable" style="width: 60%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 60%; text-align:center;"  
 
!style="width: 33%"|Study
 
!style="width: 33%"|Study
Line 1,134: Line 1,184:
 
!style="width: 33%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 33%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
|-
 
|-
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6113428/ Osumi et al. 2018]
+
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4481136/ Le et al. 2015 (KEYNOTE-016)]
|2011-2014
+
|2013-2016
| style="background-color:#91cf61" |Phase 2
+
| style="background-color:#ffffbe" |Phase 2, <20 pts of this subtype
 +
|-
 +
|[https://doi.org/10.1200/JCO.2017.72.5952 Ott et al. 2017b (KEYNOTE-028)]
 +
|NR
 +
|style="background-color:#91cf61"|Phase 1b
 
|-
 
|-
 
|}
 
|}
<div class="toccolours" style="background-color:#fdcdac">
+
''Note: KEYNOTE-016 was an expansion to a CRC-specific trial.''
====Prior treatment criteria====
 
*Exposure to fluoropyrimidine‐ and oxaliplatin‐based chemotherapy, with treatment failure
 
</div>
 
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
====Chemotherapy====
+
====Immunotherapy====
*[[Irinotecan (Camptosar)]] 150 mg/m<sup>2</sup> IV once on day 1
+
*[[Pembrolizumab (Keytruda)]] 10 mg/kg IV once on day 1
====Targeted therapy====
+
'''14-day cycle for up to 52 cycles (2 years)'''
*[[Cetuximab (Erbitux)]] 500 mg/m<sup>2</sup> IV over 2 hours once on day 1
 
**Subsequent doses are given over 60 minutes
 
====Supportive therapy====
 
*[[:Category:Antihistamines|Antihistamine]] prior to [[Cetuximab (Erbitux)]]
 
'''14-day cycles'''
 
 
</div></div><br>
 
</div></div><br>
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen variant #4, 180/250, bi-weekly, with response adaptation {{#subobject:7c9e16|Variant=1}}===
+
===Regimen variant #2, q3wk {{#subobject:87fj18|Variant=1}}===
 
{| class="wikitable sortable" style="width: 60%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 60%; text-align:center;"  
 
!style="width: 33%"|Study
 
!style="width: 33%"|Study
Line 1,160: Line 1,206:
 
!style="width: 33%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 33%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
|-
 
|-
|[https://doi.org/10.1200/JCO.2011.40.9243 Van Cutsem et al. 2012 (EVEREST)]
+
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8887941/ O'Malley et al. 2022 (KEYNOTE-158)]
|2004-2005
+
|2016-2020
| style="background-color:#91cf61" |Non-randomized portion of phase 1/2 RCT
+
|style="background-color:#91cf61"|Phase 2 (RT)
 
|-
 
|-
 
|}
 
|}
 
<div class="toccolours" style="background-color:#fdcdac">
 
<div class="toccolours" style="background-color:#fdcdac">
====Prior treatment criteria====
+
====Biomarker eligibility criteria====
*Exposure to irinotecan-containing chemotherapy
+
*Cohort K: MSI-H/dMMR endometrial cancer
 
</div>
 
</div>
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
====Chemotherapy====
+
====Immunotherapy====
*[[Irinotecan (Camptosar)]] 180 mg/m<sup>2</sup> IV over 30 minutes once per day on days 1 & 15
+
*[[Pembrolizumab (Keytruda)]] 200 mg IV once on day 1
 +
'''21-day cycle for up to 35 cycles (2 years)'''
 +
</div></div>
 +
===References===
 +
# '''KEYNOTE-028:''' Ott PA, Bang YJ, Berton-Rigaud D, Elez E, Pishvaian MJ, Rugo HS, Puzanov I, Mehnert JM, Aung KL, Lopez J, Carrigan M, Saraf S, Chen M, Soria JC. Safety and antitumor activity of pembrolizumab in advanced programmed death ligand 1-positive endometrial cancer: results from the KEYNOTE-028 study. J Clin Oncol. 2017 Aug 1;35(22):2535-2541. Epub 2017 May 10. [https://doi.org/10.1200/JCO.2017.72.5952 link to original article] '''contains dosing details in abstract''' [https://pubmed.ncbi.nlm.nih.gov/28489510 PubMed] NCT02054806
 +
# '''KEYNOTE-016:''' Le DT, Uram JN, Wang H, Bartlett BR, Kemberling H, Eyring AD, Skora AD, Luber BS, Azad NS, Laheru D, Biedrzycki B, Donehower RC, Zaheer A, Fisher GA, Crocenzi TS, Lee JJ, Duffy SM, Goldberg RM, de la Chapelle A, Koshiji M, Bhaijee F, Huebner T, Hruban RH, Wood LD, Cuka N, Pardoll DM, Papadopoulos N, Kinzler KW, Zhou S, Cornish TC, Taube JM, Anders RA, Eshleman JR, Vogelstein B, Diaz LA Jr. PD-1 blockade in tumors with mismatch-repair deficiency. N Engl J Med. 2015 Jun 25;372(26):2509-20. Epub 2015 May 30. [https://doi.org/10.1056/NEJMoa1500596 link to original article] '''contains dosing details in abstract''' [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4481136/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/26028255 PubMed] NCT01876511
 +
## '''Update:''' Le DT, Durham JN, Smith KN, Wang H, Bartlett BR, Aulakh LK, Lu S, Kemberling H, Wilt C, Luber BS, Wong F, Azad NS, Rucki AA, Laheru D, Donehower R, Zaheer A, Fisher GA, Crocenzi TS, Lee JJ, Greten TF, Duffy AG, Ciombor KK, Eyring AD, Lam BH, Joe A, Kang SP, Holdhoff M, Danilova L, Cope L, Meyer C, Zhou S, Goldberg RM, Armstrong DK, Bever KM, Fader AN, Taube J, Housseau F, Spetzler D, Xiao N, Pardoll DM, Papadopoulos N, Kinzler KW, Eshleman JR, Vogelstein B, Anders RA, Diaz LA Jr. Mismatch repair deficiency predicts response of solid tumors to PD-1 blockade. Science. 2017 Jul 28;357(6349):409-413. Epub 2017 Jun 8. [http://science.sciencemag.org/content/357/6349/409.long link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5576142/ link to PMC article] '''contains dosing details in supplement''' [https://pubmed.ncbi.nlm.nih.gov/28596308 PubMed]
 +
# '''KEYNOTE-158:''' O'Malley DM, Bariani GM, Cassier PA, Marabelle A, Hansen AR, De Jesus Acosta A, Miller WH Jr, Safra T, Italiano A, Mileshkin L, Xu L, Jin F, Norwood K, Maio M. Pembrolizumab in Patients With Microsatellite Instability-High Advanced Endometrial Cancer: Results From the KEYNOTE-158 Study. J Clin Oncol. 2022 Mar 1;40(7):752-761. Epub 2022 Jan 6. [https://doi.org/10.1200/jco.21.01874 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8887941/ link to PMC article] '''contains dosing details in abstract''' [https://pubmed.ncbi.nlm.nih.gov/34990208/ PubMed] NCT02628067
 +
==Temsirolimus monotherapy {{#subobject:c19c6|Regimen=1}}==
 +
<div class="toccolours" style="background-color:#eeeeee">
 +
===Regimen {{#subobject:53c722|Variant=1}}===
 +
{| class="wikitable" style="width: 40%; text-align:center;"
 +
!style="width: 25%"|Study
 +
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 +
|-
 +
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3158598/ Oza et al. 2011 (NCIC IND.160)]
 +
|style="background-color:#91cf61"|Phase 2
 +
|-
 +
|}
 +
<div class="toccolours" style="background-color:#b3e2cd">
 
====Targeted therapy====
 
====Targeted therapy====
*[[Cetuximab (Erbitux)]] 400 mg/m<sup>2</sup> IV once on day 1, then 250 mg/m<sup>2</sup> IV once per day on days 8 & 15
+
*[[Temsirolimus (Torisel)]] 25 mg IV over 30 minutes once per day on days 1, 8, 15, 22
'''21-day course'''
+
'''28-day cycles'''
</div>
+
</div></div>
<div class="toccolours" style="background-color:#cbd5e7">
+
===References===
====Subsequent treatment====
+
# '''NCIC IND.160:''' Oza AM, Elit L, Tsao MS, Kamel-Reid S, Biagi J, Provencher DM, Gotlieb WH, Hoskins PJ, Ghatage P, Tonkin KS, Mackay HJ, Mazurka J, Sederias J, Ivy P, Dancey JE, Eisenhauer EA; NCIC Clinical Trials Group. Phase II study of temsirolimus in women with recurrent or metastatic endometrial cancer: a trial of the NCIC Clinical Trials Group. J Clin Oncol. 2011 Aug 20;29(24):3278-85. Epub 2011 Jul 25. [https://doi.org/10.1200/jco.2010.34.1578 link to original article] '''contains dosing details in manuscript''' [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3158598/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/21788564 PubMed] NCT00072176
*EVEREST, grade 0 or 1 skin reaction: Continue standard dose versus escalate dose of cetuximab to 500 mg/m<sup>2</sup>
+
==Topotecan monotherapy {{#subobject:9a02a0|Regimen=1}}==
*EVEREST, grade 2 or worse skin reaction: Continue standard dose
 
</div></div><br>
 
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen variant #5, 180/500, bi-weekly {{#subobject:3062ba|Variant=1}}===
+
===Regimen {{#subobject:1c2f98|Variant=1}}===
{| class="wikitable sortable" style="width: 60%; text-align:center;"  
+
{| class="wikitable" style="width: 40%; text-align:center;"  
!style="width: 33%"|Study
+
!style="width: 25%"|Study
!style="width: 33%"|Years of enrollment
+
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
!style="width: 33%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
 
|-
 
|-
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2527794/ Martín-Martorell et al. 2008]
+
|[https://doi.org/10.1200/jco.2003.12.093 Wadler et al. 2003 (ECOG E3E93)]
|2005-2007
+
|style="background-color:#91cf61"|Phase 2
| style="background-color:#91cf61" |Phase 2
 
 
|-
 
|-
 
|}
 
|}
<div class="toccolours" style="background-color:#fdcdac">
 
====Prior treatment criteria====
 
*One previous line of chemotherapy
 
</div>
 
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
*[[Irinotecan (Camptosar)]] 180 mg/m<sup>2</sup> IV over 30 minutes once on day 1
+
*[[Topotecan (Hycamtin)]] 1.5 mg/m<sup>2</sup> IV once per day on days 1 to 5
====Targeted therapy====
+
**Dosage for patients with previous pelvic radiation: 1.2 mg/m<sup>2</sup>, which can be increased to the 1.5 mg/m<sup>2</sup> dose in later cycles if there are no toxicities higher than grade 1
*[[Cetuximab (Erbitux)]] 500 mg/m<sup>2</sup> IV over 2 hours once on day 1
+
'''21-day cycles'''
**If tolerated, subsequent doses can be given over 1 hour
+
</div></div>
====Supportive therapy====
+
===References===
*[[:Category:Antihistamines|Antihistamine]] prior to [[Cetuximab (Erbitux)]]
+
# '''ECOG E3E93:''' Wadler S, Levy DE, Lincoln ST, Soori GS, Schink JC, Goldberg G. Topotecan is an active agent in the first-line treatment of metastatic or recurrent endometrial carcinoma: Eastern Cooperative Oncology Group Study E3E93. J Clin Oncol. 2003 Jun 1;21(11):2110-4. [https://doi.org/10.1200/jco.2003.12.093 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/12775736 PubMed]
*[[Dexamethasone (Decadron)]] & [[Ondansetron (Zofran)]] prior to [[Irinotecan (Camptosar)]]
+
=Endocrine therapy for advanced, recurrent, or metastatic disease=
'''14-day cycles'''
+
==Anastrozole monotherapy {{#subobject:534a|Regimen=1}}==
</div></div><br>
+
<div class="toccolours" style="background-color:#eeeeee">
 +
===Regimen {{#subobject:8c4e67|Variant=1}}===
 +
{| class="wikitable" style="width: 40%; text-align:center;"
 +
!style="width: 25%"|Study
 +
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 +
|-
 +
|[http://www.gynecologiconcology-online.net/article/S0090-8258(00)95865-7 Rose et al. 2000]
 +
|style="background-color:#91cf61"|Phase 2
 +
|-
 +
|}
 +
<div class="toccolours" style="background-color:#b3e2cd">
 +
====Endocrine therapy====
 +
*[[Anastrozole (Arimidex)]] 1 mg PO once per day
 +
'''Continued indefinitely'''
 +
</div></div>
 +
===References===
 +
# Rose PG, Brunetto VL, VanLe L, Bell J, Walker JL, Lee RB; Gynecologic Oncology Group. A phase II trial of anastrozole in advanced recurrent or persistent endometrial carcinoma: a Gynecologic Oncology Group study. Gynecol Oncol. 2000 Aug;78(2):212-6. [http://www.gynecologiconcology-online.net/article/S0090-8258(00)95865-7 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/10926805 PubMed]
 +
==Medroxyprogesterone monotherapy {{#subobject:6c7bb9|Regimen=1}}==
 +
<div class="toccolours" style="background-color:#eeeeee">
 +
===Regimen {{#subobject:8b5e67|Variant=1}}===
 +
{| class="wikitable sortable" style="width: 100%; text-align:center;"
 +
!style="width: 20%"|Study
 +
!style="width: 20%"|Years of enrollment
 +
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 +
!style="width: 20%"|Comparator
 +
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 +
|-
 +
|[https://doi.org/10.1056/NEJM196102022640503 Kelley & Baker 1961]
 +
|1950-1959
 +
| style="background-color:#91cf61" |Non-randomized
 +
| style="background-color:#d3d3d3" |
 +
| style="background-color:#d3d3d3" |
 +
|-
 +
|[https://doi.org/10.1200/jco.1999.17.6.1736 Thigpen et al. 1999]
 +
|1985-1989
 +
|style="background-color:#1a9851"|Phase 3 (C)
 +
|[[#Medroxyprogesterone_monotherapy|Medroxyprogesterone]]; high-dose
 +
|style="background-color:#ffffbf"|Did not meet primary endpoint of ORR
 +
|-
 +
|}
 +
''Note: to our knowledge, this regimen was not tested as an experimental arm in an RCT in this context, prior to becoming a standard comparator arm. Kelley & Baker 1961 examined a variety of progestins and is included for historic interest.''
 +
<div class="toccolours" style="background-color:#b3e2cd">
 +
====Endocrine therapy====
 +
*[[Medroxyprogesterone (MPA)]] 200 mg PO once per day
 +
'''Continued indefinitely'''
 +
</div></div>
 +
===References===
 +
# Kelley RM, Baker WH. Progestational agents in the treatment of carcinoma of the endometrium. N Engl J Med. 1961 Feb 2;264:216-22. [https://doi.org/10.1056/NEJM196102022640503 link to original article] [https://pubmed.ncbi.nlm.nih.gov/13752346 PubMed]
 +
# Thigpen JT, Brady MF, Alvarez RD, Adelson MD, Homesley HD, Manetta A, Soper JT, Given FT; Gynecologic Oncology Group. Oral medroxyprogesterone acetate in the treatment of advanced or recurrent endometrial carcinoma: a dose-response study by the Gynecologic Oncology Group. J Clin Oncol. 1999 Jun;17(6):1736-44. [https://doi.org/10.1200/jco.1999.17.6.1736 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/10561210 PubMed]
 +
==Medroxyprogesterone & Tamoxifen {{#subobject:60584d|Regimen=1}}==
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen variant #6, 350/250, q3wk irinotecan {{#subobject:ada904|Variant=1}}===
+
===Regimen {{#subobject:334b8c|Variant=1}}===
{| class="wikitable" style="color:white; background-color:#404040"
+
{| class="wikitable" style="width: 40%; text-align:center;"
|<small>'''FDA-recommended dose'''</small>
+
!style="width: 25%"|Study
 +
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 +
|-
 +
|[http://www.gynecologiconcology-online.net/article/S0090-8258(03)00651-6 Whitney et al. 2004]
 +
|style="background-color:#91cf61"|Phase 2
 
|-
 
|-
 
|}
 
|}
 +
<div class="toccolours" style="background-color:#b3e2cd">
 +
====Endocrine therapy====
 +
*[[Medroxyprogesterone (MPA)]] 100 mg PO twice per day on even-numbered weeks (for example, week 2, 4, 6, etc.)
 +
*[[Tamoxifen (Nolvadex)]] 20 mg PO twice per day
 +
'''Continued indefinitely'''
 +
</div></div>
 +
===References===
 +
# Whitney CW, Brunetto VL, Zaino RJ, Lentz SS, Sorosky J, Armstrong DK, Lee RB; Gynecologic Oncology Group. Phase II study of medroxyprogesterone acetate plus tamoxifen in advanced endometrial carcinoma: a Gynecologic Oncology Group study. Gynecol Oncol. 2004 Jan;92(1):4-9. [http://www.gynecologiconcology-online.net/article/S0090-8258(03)00651-6 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/14751130 PubMed]
 +
==Megestrol monotherapy {{#subobject:4b50ea|Regimen=1}}==
 +
<div class="toccolours" style="background-color:#eeeeee">
 +
===Regimen {{#subobject:52dc53|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
Line 1,221: Line 1,342:
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
|-
 
|-
|[https://doi.org/10.1056/NEJMoa033025 Cunningham et al. 2004 (BOND)]
+
|[https://doi.org/10.1056/NEJM196102022640503 Kelley & Baker 1961]
|2001-2002
+
|1950-1959
| style="background-color:#1a9851" |Phase 3 (E-RT-esc)
+
| style="background-color:#91cf61" |Non-randomized
|[[#Cetuximab_monotherapy_2|Cetuximab]]
+
| style="background-color:#d3d3d3" |
| style="background-color:#1a9850" |Superior TTP
+
| style="background-color:#d3d3d3" |
 +
|-
 +
|[http://journals.lww.com/amjclinicaloncology/Fulltext/2001/02000/Megestrol_and_Tamoxifen_in_Patients_With_Advanced.7.aspx Pandya et al. 2001 (ECOG E4882)]
 +
|1982-1984
 +
|style="background-color:#1a9851"|Randomized Phase 2 (C)
 +
|[[#Megestrol_.26_Tamoxifen|Megestrol & Tamoxifen]]
 +
|style="background-color:#ffffbf"|Did not meet efficacy endpoints
 
|-
 
|-
 
|}
 
|}
''Note that the FDA-recommended dosing is for the cetuximab component; no comment is made about irinotecan dosing.''
+
''Note: to our knowledge, this regimen was not tested as an experimental arm in an RCT in this context, prior to becoming a standard comparator arm. Kelley & Baker 1961 examined a variety of progestins and is included for historic interest.''
<div class="toccolours" style="background-color:#fdcdac">
 
====Prior treatment criteria====
 
*BOND: Exposure to irinotecan-containing therapy, with progression
 
</div>
 
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
====Chemotherapy====
+
====Endocrine therapy====
*[[Irinotecan (Camptosar)]] 350 mg/m<sup>2</sup> IV over 90 minutes once on day 1
+
*[[Megestrol (Megace)]] 80 mg PO twice per day
**If aged 70 years old or more, [[Performance status|ECOG performance status]] 2 or more, or prior pelvic radiation: 300 mg/m<sup>2</sup> IV over 90 minutes once on day 1
+
'''Continued indefinitely'''
====Targeted therapy====
 
*[[Cetuximab (Erbitux)]] as follows:
 
**Cycle 1: 400 mg/m<sup>2</sup> IV over 2 hours once on day 1, then 250 mg/m<sup>2</sup> IV over 60 minutes once per day on days 8 & 15
 
**Cycle 2 onwards: 250 mg/m<sup>2</sup> IV over 60 minutes once per day on days 1, 8, 15
 
====Supportive therapy====
 
*[[:Category:Antihistamines|Antihistamine]] prior to at least the first infusion of [[Cetuximab (Erbitux)]]
 
'''21-day cycles'''
 
 
</div></div>
 
</div></div>
 
===References===
 
===References===
#'''BOND:''' Cunningham D, Humblet Y, Siena S, Khayat D, Bleiberg H, Santoro A, Bets D, Mueser M, Harstrick A, Verslype C, Chau I, Van Cutsem E. Cetuximab monotherapy and cetuximab plus irinotecan in irinotecan-refractory metastatic colorectal cancer. N Engl J Med. 2004 Jul 22;351(4):337-45. [https://doi.org/10.1056/NEJMoa033025 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/15269313 PubMed]
+
# Kelley RM, Baker WH. Progestational agents in the treatment of carcinoma of the endometrium. N Engl J Med. 1961 Feb 2;264:216-22. [https://doi.org/10.1056/NEJM196102022640503 link to original article] [https://pubmed.ncbi.nlm.nih.gov/13752346 PubMed]
#Martín-Martorell P, Roselló S, Rodríguez-Braun E, Chirivella I, Bosch A, Cervantes A. Biweekly cetuximab and irinotecan in advanced colorectal cancer patients progressing after at least one previous line of chemotherapy: results of a phase II single institution trial. Br J Cancer. 2008 Aug 5;99(3):455-8. [https://doi.org/10.1038/sj.bjc.6604530 link to original article] '''contains dosing details in manuscript''' [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2527794/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/18665167 PubMed]
+
# '''ECOG E4882:''' Pandya KJ, Yeap BY, Weiner LM, Krook JE, Erban JK, Schinella RA, Davis TE. Megestrol and tamoxifen in patients with advanced endometrial cancer: an Eastern Cooperative Oncology Group Study (E4882). Am J Clin Oncol. 2001 Feb;24(1):43-6. [http://journals.lww.com/amjclinicaloncology/Fulltext/2001/02000/Megestrol_and_Tamoxifen_in_Patients_With_Advanced.7.aspx link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/11232948 PubMed]
#'''EVEREST:''' Van Cutsem E, Tejpar S, Vanbeckevoort D, Peeters M, Humblet Y, Gelderblom H, Vermorken JB, Viret F, Glimelius B, Gallerani E, Hendlisz A, Cats A, Moehler M, Sagaert X, Vlassak S, Schlichting M, Ciardiello F. Intrapatient cetuximab dose escalation in metastatic colorectal cancer according to the grade of early skin reactions: the randomized EVEREST study. J Clin Oncol. 2012 Aug 10;30(23):2861-8. Epub 2012 Jul 2. [https://doi.org/10.1200/JCO.2011.40.9243 link to original article] '''contains dosing details in abstract''' [https://pubmed.ncbi.nlm.nih.gov/22753904 PubMed]
+
==Megestrol & Tamoxifen {{#subobject:f03c30|Regimen=1}}==
#Osumi H, Shinozaki E, Mashima T, Wakatsuki T, Suenaga M, Ichimura T, Ogura M, Ota Y, Nakayama I, Takahari D, Chin K, Miki Y, Yamaguchi K. Phase II trial of biweekly cetuximab and irinotecan as third-line therapy for pretreated KRAS exon 2 wild-type colorectal cancer. Cancer Sci. 2018 Aug;109(8):2567-2575. Epub 2018 Jul 13. [https://doi.org/full/10.1111/cas.13698 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6113428/ link to PMC article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/29908105 PubMed] UMIN000019893
 
==Panitumumab monotherapy {{#subobject:5a3eb5|Regimen=1}}==
 
===Example orders===
 
*[[Example orders for Panitumumab (Vectibix) in colon cancer]]
 
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen {{#subobject:fa978e|Variant=1}}===
+
===Regimen {{#subobject:4e79f7|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
Line 1,262: Line 1,374:
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
|-
 
|-
|[https://doi.org/10.1200/jco.2006.08.1620 Van Cutsem et al. 2007 (20020408)]
+
|[http://journals.lww.com/amjclinicaloncology/Fulltext/2001/02000/Megestrol_and_Tamoxifen_in_Patients_With_Advanced.7.aspx Pandya et al. 2001 (ECOG E4882)]
|2004-2005
+
|1982-1984
| style="background-color:#1a9851" |Phase 3 (E-RT-esc)
+
|style="background-color:#1a9851"|Randomized Phase 2 (E-switch-ic)
|[[Colon_cancer_-_null_regimens#Best_supportive_care_2|Best supportive care]]
+
|[[#Megestrol_monotherapy|Megestrol]]
| style="background-color:#1a9850" |Superior PFS<br>Median PFS: 8 vs 7.3 wks<br>(HR 0.54, 95% CI 0.44-0.66)
+
|style="background-color:#ffffbf"|Did not meet primary efficacy endpoints
 +
|-
 +
|[http://www.gynecologiconcology-online.net/article/S0090-8258(03)00787-X Fiorica et al. 2004]
 +
|1994-1995
 +
| style="background-color:#91cf61" |Phase 2
 +
| style="background-color:#d3d3d3" |
 +
| style="background-color:#d3d3d3" |
 
|-
 
|-
|[https://doi.org/10.1016/S1470-2045(14)70118-4 Price et al. 2014 (ASPECCT)]
+
|}
|2010-2012
+
<div class="toccolours" style="background-color:#b3e2cd">
| style="background-color:#1a9851" |Phase 3 (E-RT-switch-ic)
+
====Endocrine therapy, part 1====
|[[#Cetuximab_monotherapy_2|Cetuximab]]
+
*[[Megestrol (Megace)]] 80 mg PO twice per day
| style="background-color:#eeee01" |Non-inferior OS
+
'''21-day cycles, alternating with tamoxifen'''
 +
====Endocrine therapy, part 2====
 +
*[[Tamoxifen (Nolvadex)]] 20 mg PO twice per day
 +
'''21-day cycles, alternating with megestrol'''
 +
</div></div>
 +
===References===
 +
# '''ECOG E4882:''' Pandya KJ, Yeap BY, Weiner LM, Krook JE, Erban JK, Schinella RA, Davis TE. Megestrol and tamoxifen in patients with advanced endometrial cancer: an Eastern Cooperative Oncology Group Study (E4882). Am J Clin Oncol. 2001 Feb;24(1):43-6. [http://journals.lww.com/amjclinicaloncology/Fulltext/2001/02000/Megestrol_and_Tamoxifen_in_Patients_With_Advanced.7.aspx link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/11232948 PubMed]
 +
# Fiorica JV, Brunetto VL, Hanjani P, Lentz SS, Mannel R, Andersen W; Gynecologic Oncology Group. Phase II trial of alternating courses of megestrol acetate and tamoxifen in advanced endometrial carcinoma: a Gynecologic Oncology Group study. Gynecol Oncol. 2004 Jan;92(1):10-4. [http://www.gynecologiconcology-online.net/article/S0090-8258(03)00787-X link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/14751131 PubMed]
 +
==Tamoxifen monotherapy {{#subobject:ab84a1|Regimen=1}}==
 +
<div class="toccolours" style="background-color:#eeeeee">
 +
===Regimen {{#subobject:af71e3|Variant=1}}===
 +
{| class="wikitable" style="width: 40%; text-align:center;"
 +
!style="width: 25%"|Study
 +
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 +
|-
 +
|[http://www.gynecologiconcology-online.net/article/0090-8258(89)90839-1/pdf Quinn et al. 1989]
 +
|style="background-color:#91cf61"|Phase 2
 
|-
 
|-
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5104888/ Kim et al. 2016 (20100007)]
+
|[https://doi.org/10.1200/jco.2001.19.2.364 Thigpen et al. 2001 (GOG-81F)]
|2011-2013
+
|style="background-color:#91cf61"|Phase 2
| style="background-color:#1a9851" |Phase 3 (E-RT-esc)
 
|[[Colon_cancer_-_null_regimens#Best_supportive_care_2|Best supportive care]]
 
| style="background-color:#1a9850" |Superior OS<sup>1</sup><br>Median OS: 10 vs 6.9 mo<br>(HR 0.72, 95% CI 0.55-0.94)
 
 
|-
 
|-
 
|}
 
|}
''<sup>1</sup>Reported efficacy for 20100007 is based on the 2018 update.''
 
<div class="toccolours" style="background-color:#fdcdac">
 
====Prior treatment criteria====
 
*20020408 & 20100007: Exposure to irinotecan, oxaliplatin, and a fluoropyrimidine
 
</div>
 
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
====Targeted therapy====
+
====Endocrine therapy====
*[[Panitumumab (Vectibix)]] 6 mg/kg IV over 60 minutes once on day 1
+
*[[Tamoxifen (Nolvadex)]] 20 mg PO twice per day
'''14-day cycles'''
+
'''Continued indefinitely'''
 
</div></div>
 
</div></div>
 
===References===
 
===References===
<!-- Presented at the 97th Annual Meeting of the American Association for Cancer Research, April 1-5, 2006, Washington, DC; 2nd Annual Conference of the Hematology/Oncology Pharmacy Association, June 15-18, 2006, Orlando, FL; 8th Annual Conference of the World Congress on Gastrointestinal Cancer, June 28-July 1, 2006, Barcelona, Spain; and at the 31st European Society of Medical Oncology Congress, September 29-October 3, 2006, Istanbul, Turkey. -->
+
# Quinn MA, Campbell JJ. Tamoxifen therapy in advanced/recurrent endometrial carcinoma. Gynecol Oncol. 1989 Jan;32(1):1-3. [http://www.gynecologiconcology-online.net/article/0090-8258(89)90839-1/pdf link to original article] [https://pubmed.ncbi.nlm.nih.gov/2909443 PubMed]
#'''20020408:''' Van Cutsem E, Peeters M, Siena S, Humblet Y, Hendlisz A, Neyns B, Canon JL, Van Laethem JL, Maurel J, Richardson G, Wolf M, Amado RG. Open-label phase III trial of panitumumab plus best supportive care compared with best supportive care alone in patients with chemotherapy-refractory metastatic colorectal cancer. J Clin Oncol. 2007 May 1;25(13):1658-64. [https://doi.org/10.1200/jco.2006.08.1620 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/17470858 PubMed] NCT00113763
+
# '''GOG-81F:''' Thigpen T, Brady MF, Homesley HD, Soper JT, Bell J. Tamoxifen in the treatment of advanced or recurrent endometrial carcinoma: a Gynecologic Oncology Group study. J Clin Oncol. 2001 Jan 15;19(2):364-7. [https://doi.org/10.1200/jco.2001.19.2.364 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/11208827 PubMed]
#'''ASPECCT:''' Price TJ, Peeters M, Kim TW, Li J, Cascinu S, Ruff P, Suresh AS, Thomas A, Tjulandin S, Zhang K, Murugappan S, Sidhu R. Panitumumab versus cetuximab in patients with chemotherapy-refractory wild-type KRAS exon 2 metastatic colorectal cancer (ASPECCT): a randomised, multicentre, open-label, non-inferiority phase 3 study. Lancet Oncol. 2014 May;15(6):569-79. Epub 2014 Apr 14. [https://doi.org/10.1016/S1470-2045(14)70118-4 link to original article] [https://pubmed.ncbi.nlm.nih.gov/24739896 PubMed] NCT01001377
+
[[Category:Endometrial cancer regimens]]
##'''Update:''' Price T, Kim TW, Li J, Cascinu S, Ruff P, Suresh AS, Thomas A, Tjulandin S, Guan X, Peeters M. Final results and outcomes by prior bevacizumab exposure, skin toxicity, and hypomagnesaemia from ASPECCT: randomized phase 3 non-inferiority study of panitumumab versus cetuximab in chemorefractory wild-type KRAS exon 2 metastatic colorectal cancer. Eur J Cancer. 2016 Nov;68:51-59. Epub 2016 Oct 5. [https://doi.org/10.1016/j.ejca.2016.08.010 link to original article] [https://pubmed.ncbi.nlm.nih.gov/27716478 PubMed]
+
[[Category:Disease-specific pages]]
#'''20100007:''' Kim TW, Elme A, Kusic Z, Park JO, Udrea AA, Kim SY, Ahn JB, Valencia RV, Krishnan S, Bilic A, Manojlovic N, Dong J, Guan X, Lofton-Day C, Jung AS, Vrdoljak E. A phase 3 trial evaluating panitumumab plus best supportive care vs best supportive care in chemorefractory wild-type KRAS or RAS metastatic colorectal cancer. Br J Cancer. 2016 Nov 8;115(10):1206-1214. Epub 2016 Oct 13. [https://doi.org/10.1038/bjc.2016.309 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5104888/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/27736842 PubMed] NCT01412957
+
[[Category:Gynecologic cancers]]
##'''Update:''' Kim TW, Elme A, Park JO, Udrea AA, Kim SY, Ahn JB, Valencia RV, Krishnan S, Manojlovic N, Guan X, Lofton-Day C, Jung AS, Vrdoljak E. Final Analysis of Outcomes and RAS/BRAF Status in a Randomized Phase 3 Study of Panitumumab and Best Supportive Care in Chemorefractory Wild Type KRAS Metastatic Colorectal Cancer. Clin Colorectal Cancer. 2018 Sep;17(3):206-214. Epub 2018 Mar 21. [https://www.clinical-colorectal-cancer.com/article/S1533-0028(17)30529-7 link to original article] [https://pubmed.ncbi.nlm.nih.gov/29703606 PubMed]
 
[[Category:Colorectal cancer regimens]]
 
[[Category:Biomarker-specific pages]]
 
[[Category:Gastrointestinal cancers]]
 

Revision as of 01:06, 14 October 2022

Section editor transclusions Are you looking for a regimen but can't find it here? For placebo or observational studies in this condition, please visit this page. If you still can't find it, please let us know so we can add it!

35 regimens on this page
55 variants on this page


Guidelines

ESMO

Older

NCCN

Adjuvant therapy

Carboplatin & Paclitaxel (CP)

Regimen variant #1, 5/175 x 4

Study Years of enrollment Evidence Comparator Comparative Efficacy
de Boer et al. 2018 (PORTEC-3) 2006-2013 Phase 3 (E-esc) See link See link

Preceding treatment

Chemotherapy

21-day cycle for 4 cycles


Regimen variant #2, 6/175 x 6

Study Years of enrollment Evidence Comparator Comparative Efficacy
Matei et al. 2019 (GOG 258) 2009-2014 Phase 3 (C) Cisplatin & RT, then CP x 4 Did not meet primary endpoint of RFS

Preceding treatment

Chemotherapy

21-day cycle for 6 cycles

References

  1. PORTEC-3: de Boer SM, Powell ME, Mileshkin L, Katsaros D, Bessette P, Haie-Meder C, Ottevanger PB, Ledermann JA, Khaw P, Colombo A, Fyles A, Baron MH, Jürgenliemk-Schulz IM, Kitchener HC, Nijman HW, Wilson G, Brooks S, Carinelli S, Provencher D, Hanzen C, Lutgens LCHW, Smit VTHBM, Singh N, Do V, D'Amico R, Nout RA, Feeney A, Verhoeven-Adema KW, Putter H, Creutzberg CL; PORTEC study group. Adjuvant chemoradiotherapy versus radiotherapy alone for women with high-risk endometrial cancer (PORTEC-3): final results of an international, open-label, multicentre, randomised, phase 3 trial. Lancet Oncol. 2018 Mar;19(3):295-309. Epub 2018 Feb 12. link to original article link to PMC article PubMed NCT00411138
    1. Update: de Boer SM, Powell ME, Mileshkin L, Katsaros D, Bessette P, Haie-Meder C, Ottevanger PB, Ledermann JA, Khaw P, D'Amico R, Fyles A, Baron MH, Jürgenliemk-Schulz IM, Kitchener HC, Nijman HW, Wilson G, Brooks S, Gribaudo S, Provencher D, Hanzen C, Kruitwagen RF, Smit VTHBM, Singh N, Do V, Lissoni A, Nout RA, Feeney A, Verhoeven-Adema KW, Putter H, Creutzberg CL; PORTEC Study Group. Adjuvant chemoradiotherapy versus radiotherapy alone in women with high-risk endometrial cancer (PORTEC-3): patterns of recurrence and post-hoc survival analysis of a randomised phase 3 trial. Lancet Oncol. 2019 Sep;20(9):1273-1285. Epub 2019 Jul 22. Erratum in: Lancet Oncol. 2019 Sep;20(9):e468. link to original article contains dosing details in manuscript PubMed
  2. GOG 258: Matei D, Filiaci V, Randall ME, Mutch D, Steinhoff MM, DiSilvestro PA, Moxley KM, Kim YM, Powell MA, O'Malley DM, Spirtos NM, Small W Jr, Tewari KS, Richards WE, Nakayama J, Matulonis UA, Huang HQ, Miller DS. Adjuvant chemotherapy plus radiation for locally advanced endometrial cancer. N Engl J Med. 2019 Jun 13;380(24):2317-2326. link to original article contains dosing details in manuscript PubMed NCT00942357
  3. JGOG2043: Nomura H, Aoki D, Michimae H, Mizuno M, Nakai H, Arai M, Sasagawa M, Ushijima K, Sugiyama T, Saito M, Tokunaga H, Matoda M, Nakanishi T, Watanabe Y, Takahashi F, Saito T, Yaegashi N; Japanese Gynecologic Oncology Group. Effect of Taxane Plus Platinum Regimens vs Doxorubicin Plus Cisplatin as Adjuvant Chemotherapy for Endometrial Cancer at a High Risk of Progression: A Randomized Clinical Trial. JAMA Oncol. 2019 Jun 1;5(6):833-840. Epub 2019 Mar 21. link to original article contains dosing details in manuscript link to PMC article PubMed UMIN000000522
  4. KEYNOTE-B21: NCT04634877

CIM

CIM: Cisplatin, Ifosfamide, Mesna

Regimen

Study Years of enrollment Evidence Comparator Comparative Efficacy
Wolfson et al. 2007 (GOG 150) 1993-2005 Phase 3 (E-switch-ooc) Whole abdominal irradiation Might have superior OS1
Median OS: 48 vs 24 mo
(HR 0.71, 95% CI 0.48-1.05)

1Median OS is not reported in the paper and is estimated from the K-M curve.

Preceding treatment

Chemotherapy

  • Cisplatin (Platinol) 20 mg/m2 IV once per day on days 1 to 4, given first, at an infusion rate of approximately 1 mg/min
  • Ifosfamide (Ifex) 1500 mg/m2 IV over 60 minutes once per day on days 1 to 4, given second, with mesna

Supportive therapy

  • Mesna (Mesnex) 120 mg/m2 IV over 15 minutes once on day 1, then 1500 mg/m2/day IV continuous infusion over 96 hours, given second, with Ifosfamide (Ifex)
  • Suggested hydration: 1 liter of NS or 1/2 NS over several hours once per day on days 1 to 4, prior to chemotherapy

21-day cycle for 3 cycles

References

  1. GOG 150: Wolfson AH, Brady MF, Rocereto T, Mannel RS, Lee YC, Futoran RJ, Cohn DE, Ioffe OB. A Gynecologic Oncology Group randomized phase III trial of whole abdominal irradiation (WAI) vs cisplatin-ifosfamide and mesna (CIM) as post-surgical therapy in stage I-IV carcinosarcoma (CS) of the uterus. Gynecol Oncol. 2007 Nov;107(2):177-85. Epub 2007 Sep 5. link to original article contains dosing details in manuscript link to PMC article PubMed NCT00002546

Cisplatin & Doxorubicin

CD: Cisplatin & Doxorubicin
AP: Adriamycin (Doxorubicin) & Platinol (Cisplatin)

Regimen variant #1, 50/45, capped BSA

Study Years of enrollment Evidence Comparator Comparative Efficacy
Homesley et al. 2008 (GOG 184) 2000-2004 Phase 3 (C) CDP Did not meet primary endpoint of RFS

Note: Treatment was to start within 8 weeks of completion of RT.

Preceding treatment

Chemotherapy

Supportive therapy

21-day cycle for 6 cycles


Regimen variant #2, 50/60 x 6

Study Years of enrollment Evidence Comparator Comparative Efficacy
Nomura et al. 2019 (JGOG2043) 2006-2011 Phase 3 (C) 1. Carboplatin & Paclitaxel
2. Cisplatin & Docetaxel
Did not meet primary endpoint of PFS

Preceding treatment

Chemotherapy

21-day cycle for 6 cycles


Regimen variant #3, 50/60 x 8

Study Years of enrollment Evidence Comparator Comparative Efficacy
Randall et al. 2006 (GOG 122) 1992-2000 Phase 3 (E-switch-ooc) Whole abdominal irradiation Superior OS
OS60: 55% vs 42%
(aHR 0.68, 95% CI 0.52-0.89)

Preceding treatment

Chemotherapy

Supportive therapy

21-day cycle for 8 cycles

References

  1. GOG 122: Randall ME, Filiaci VL, Muss H, Spirtos NM, Mannel RS, Fowler J, Thigpen JT, Benda JA; Gynecologic Oncology Group. Randomized phase III trial of whole-abdominal irradiation versus doxorubicin and cisplatin chemotherapy in advanced endometrial carcinoma: a Gynecologic Oncology Group study. J Clin Oncol. 2006 Jan 1;24(1):36-44. Epub 2005 Dec 5. link to original article contains dosing details in manuscript PubMed
  2. GOG 184: Homesley HD, Filiaci V, Gibbons SK, Long HJ, Cella D, Spirtos NM, Morris RT, DeGeest K, Lee R, Montag A. A randomized phase III trial in advanced endometrial carcinoma of surgery and volume directed radiation followed by cisplatin and doxorubicin with or without paclitaxel: A Gynecologic Oncology Group study. Gynecol Oncol. 2009 Mar;112(3):543-52. Epub 2008 Dec 23. link to original article contains dosing details in manuscript link to PMC article PubMed NCT00006011
    1. Update: Spirtos NM, Enserro D, Homesley HD, Gibbons SK, Cella D, Morris RT, DeGeest K, Lee RB, Miller DS. The addition of paclitaxel to doxorubicin and cisplatin and volume-directed radiation does not improve overall survival (OS) or long-term recurrence-free survival (RFS) in advanced endometrial cancer (EC): a randomized phase III NRG/Gynecologic Oncology Group (GOG) study. Gynecol Oncol. 2019 Jul;154(1):13-21. Epub 2019 Apr 30. link to original article link to PMC article PubMed
  3. JGOG2043: Nomura H, Aoki D, Michimae H, Mizuno M, Nakai H, Arai M, Sasagawa M, Ushijima K, Sugiyama T, Saito M, Tokunaga H, Matoda M, Nakanishi T, Watanabe Y, Takahashi F, Saito T, Yaegashi N; Japanese Gynecologic Oncology Group. Effect of Taxane Plus Platinum Regimens vs Doxorubicin Plus Cisplatin as Adjuvant Chemotherapy for Endometrial Cancer at a High Risk of Progression: A Randomized Clinical Trial. JAMA Oncol. 2019 Jun 1;5(6):833-840. Epub 2019 Mar 21. link to original article contains dosing details in manuscript link to PMC article PubMed UMIN000000522

Cisplatin & RT

Cisplatin & RT: Cisplatin & Radiation Therapy

Regimen

Study Years of enrollment Evidence Comparator Comparative Efficacy
de Boer et al. 2018 (PORTEC-3) 2006-2013 Phase 3 (E-esc) See link See link

Note: in PORTEC-3, radiation is to start within 4 to 6 weeks after surgery, and no later than 8 weeks; reported efficacy is based on the 2019 update.

Preceding treatment

Chemotherapy

21-day cycle for 2 cycles

Radiotherapy

5.5-week course

Subsequent treatment

References

  1. PORTEC-3: de Boer SM, Powell ME, Mileshkin L, Katsaros D, Bessette P, Haie-Meder C, Ottevanger PB, Ledermann JA, Khaw P, Colombo A, Fyles A, Baron MH, Jürgenliemk-Schulz IM, Kitchener HC, Nijman HW, Wilson G, Brooks S, Carinelli S, Provencher D, Hanzen C, Lutgens LCHW, Smit VTHBM, Singh N, Do V, D'Amico R, Nout RA, Feeney A, Verhoeven-Adema KW, Putter H, Creutzberg CL; PORTEC study group. Adjuvant chemoradiotherapy versus radiotherapy alone for women with high-risk endometrial cancer (PORTEC-3): final results of an international, open-label, multicentre, randomised, phase 3 trial. Lancet Oncol. 2018 Mar;19(3):295-309. Epub 2018 Feb 12. link to original article link to PMC article PubMed NCT00411138
    1. Update: de Boer SM, Powell ME, Mileshkin L, Katsaros D, Bessette P, Haie-Meder C, Ottevanger PB, Ledermann JA, Khaw P, D'Amico R, Fyles A, Baron MH, Jürgenliemk-Schulz IM, Kitchener HC, Nijman HW, Wilson G, Brooks S, Gribaudo S, Provencher D, Hanzen C, Kruitwagen RF, Smit VTHBM, Singh N, Do V, Lissoni A, Nout RA, Feeney A, Verhoeven-Adema KW, Putter H, Creutzberg CL; PORTEC Study Group. Adjuvant chemoradiotherapy versus radiotherapy alone in women with high-risk endometrial cancer (PORTEC-3): patterns of recurrence and post-hoc survival analysis of a randomised phase 3 trial. Lancet Oncol. 2019 Sep;20(9):1273-1285. Epub 2019 Jul 22. Erratum in: Lancet Oncol. 2019 Sep;20(9):e468. link to original article contains dosing details in manuscript PubMed

Radiation therapy

RT: Radiation Therapy

Regimen

Study Years of enrollment Evidence Comparator Comparative Efficacy
Keys et al. 2004 (GOG 99) 1987-1995 Phase 3 (E-esc) Observation Superior RFS
Maggi et al. 2006 1990-1997 Phase 3 (C) CAP Did not meet primary endpoints of PFS/OS
Susumu et al. 2007 (JGOG 2033) 1994-2000 Phase 3 (C) CAP Did not meet primary endpoint of OS60
Homesley et al. 2008 (GOG 184) 2000-2004 Non-randomized portion of RCT
de Boer et al. 2018 (PORTEC-3) 2006-2013 Phase 3 (C) Cisplatin & RT, then Carboplatin & Paclitaxel Seems to have inferior OS1

1Reported efficacy for PORTEC-3 is based on the 2019 update.
Note: in PORTEC-3, radiation is to start within 4 to 6 weeks after surgery, and no later than 8 weeks.

Preceding treatment

Radiotherapy

One course

Subsequent treatment

  • GOG 184: CD x 6 versus CDP x 6

References

  1. GOG 99: Keys HM, Roberts JA, Brunetto VL, Zaino RJ, Spirtos NM, Bloss JD, Pearlman A, Maiman MA, Bell JG; Gynecologic Oncology Group. A phase III trial of surgery with or without adjunctive external pelvic radiation therapy in intermediate risk endometrial adenocarcinoma: a Gynecologic Oncology Group study. Gynecol Oncol. 2004 Mar;92(3):744-51. Erratum in: Gynecol Oncol. 2004 Jul;94(1):241-2. link to original article PubMed
  2. Maggi R, Lissoni A, Spina F, Melpignano M, Zola P, Favalli G, Colombo A, Fossati R. Adjuvant chemotherapy vs radiotherapy in high-risk endometrial carcinoma: results of a randomised trial. Br J Cancer. 2006 Aug 7;95(3):266-71. Epub 2006 Jul 25. link to original article link to PMC article PubMed
  3. JGOG 2033: Susumu N, Sagae S, Udagawa Y, Niwa K, Kuramoto H, Satoh S, Kudo R; Japanese Gynecologic Oncology Group. Randomized phase III trial of pelvic radiotherapy versus cisplatin-based combined chemotherapy in patients with intermediate- and high-risk endometrial cancer: a Japanese Gynecologic Oncology Group study. Gynecol Oncol. 2008 Jan;108(1):226-33. Epub 2007 Nov 9. link to original article PubMed
  4. GOG 184: Homesley HD, Filiaci V, Gibbons SK, Long HJ, Cella D, Spirtos NM, Morris RT, DeGeest K, Lee R, Montag A. A randomized phase III trial in advanced endometrial carcinoma of surgery and volume directed radiation followed by cisplatin and doxorubicin with or without paclitaxel: A Gynecologic Oncology Group study. Gynecol Oncol. 2009 Mar;112(3):543-52. Epub 2008 Dec 23. link to original article contains dosing details in manuscript link to PMC article PubMed NCT00006011
    1. Update: Spirtos NM, Enserro D, Homesley HD, Gibbons SK, Cella D, Morris RT, DeGeest K, Lee RB, Miller DS. The addition of paclitaxel to doxorubicin and cisplatin and volume-directed radiation does not improve overall survival (OS) or long-term recurrence-free survival (RFS) in advanced endometrial cancer (EC): a randomized phase III NRG/Gynecologic Oncology Group (GOG) study. Gynecol Oncol. 2019 Jul;154(1):13-21. Epub 2019 Apr 30. link to original article link to PMC article PubMed
  5. PORTEC-3: de Boer SM, Powell ME, Mileshkin L, Katsaros D, Bessette P, Haie-Meder C, Ottevanger PB, Ledermann JA, Khaw P, Colombo A, Fyles A, Baron MH, Jürgenliemk-Schulz IM, Kitchener HC, Nijman HW, Wilson G, Brooks S, Carinelli S, Provencher D, Hanzen C, Lutgens LCHW, Smit VTHBM, Singh N, Do V, D'Amico R, Nout RA, Feeney A, Verhoeven-Adema KW, Putter H, Creutzberg CL; PORTEC study group. Adjuvant chemoradiotherapy versus radiotherapy alone for women with high-risk endometrial cancer (PORTEC-3): final results of an international, open-label, multicentre, randomised, phase 3 trial. Lancet Oncol. 2018 Mar;19(3):295-309. Epub 2018 Feb 12. link to original article link to PMC article PubMed NCT00411138
    1. Update: de Boer SM, Powell ME, Mileshkin L, Katsaros D, Bessette P, Haie-Meder C, Ottevanger PB, Ledermann JA, Khaw P, D'Amico R, Fyles A, Baron MH, Jürgenliemk-Schulz IM, Kitchener HC, Nijman HW, Wilson G, Brooks S, Gribaudo S, Provencher D, Hanzen C, Kruitwagen RF, Smit VTHBM, Singh N, Do V, Lissoni A, Nout RA, Feeney A, Verhoeven-Adema KW, Putter H, Creutzberg CL; PORTEC Study Group. Adjuvant chemoradiotherapy versus radiotherapy alone in women with high-risk endometrial cancer (PORTEC-3): patterns of recurrence and post-hoc survival analysis of a randomised phase 3 trial. Lancet Oncol. 2019 Sep;20(9):1273-1285. Epub 2019 Jul 22. Erratum in: Lancet Oncol. 2019 Sep;20(9):e468. link to original article PubMed

Whole abdominal radiation (WAI)

Regimen

Study Years of enrollment Evidence Comparator Comparative Efficacy
Randall et al. 2006 (GOG 122) 1992-2000 Phase 3 (E-switch-ooc) Cisplatin & Doxorubicin Inferior OS
Wolfson et al. 2007 (GOG 150) 1993-2005 Phase 3 (C) CIM Might have inferior OS

Not commonly used but was a comparator arm; here for reference purposes only.

Radiotherapy

References

  1. GOG 122: Randall ME, Filiaci VL, Muss H, Spirtos NM, Mannel RS, Fowler J, Thigpen JT, Benda JA; Gynecologic Oncology Group. Randomized phase III trial of whole-abdominal irradiation versus doxorubicin and cisplatin chemotherapy in advanced endometrial carcinoma: a Gynecologic Oncology Group study. J Clin Oncol. 2006 Jan 1;24(1):36-44. Epub 2005 Dec 5. link to original article contains dosing details in manuscript PubMed
  2. GOG 150: Wolfson AH, Brady MF, Rocereto T, Mannel RS, Lee YC, Futoran RJ, Cohn DE, Ioffe OB. A Gynecologic Oncology Group randomized phase III trial of whole abdominal irradiation (WAI) vs cisplatin-ifosfamide and mesna (CIM) as post-surgical therapy in stage I-IV carcinosarcoma (CS) of the uterus. Gynecol Oncol. 2007 Nov;107(2):177-85. Epub 2007 Sep 5. link to original article contains dosing details in manuscript link to PMC article PubMed NCT00002546

Non-endocrine therapy for advanced, recurrent, or metastatic disease

Bevacizumab monotherapy

Regimen

Study Evidence
Aghajanian et al. 2011 (GOG-0229E) Phase 2

Targeted therapy

21-day cycles

References

  1. GOG-0229E: Aghajanian C, Sill MW, Darcy KM, Greer B, McMeekin DS, Rose PG, Rotmensch J, Barnes MN, Hanjani P, Leslie KK; Gynecologic Oncology Group. Phase II trial of bevacizumab in recurrent or persistent endometrial cancer: a Gynecologic Oncology Group study. J Clin Oncol. 2011 Jun 1;29(16):2259-65. Epub 2011 May 2. link to original article contains dosing details in manuscript link to PMC article PubMed NCT00301964

Carboplatin monotherapy

Regimen variant #1, 300 mg/m2

Study Evidence Efficacy
van Wijk et al. 2003 Phase 2 ORR: 13% (95% CI 6-25%)

This dosing is intended for patients previously treated with chemotherapy.

Chemotherapy

28-day cycles


Regimen variant #2, 400 mg/m2

Study Evidence Efficacy
van Wijk et al. 2003 Phase 2 ORR: 13% (95% CI 6-25%)

Chemotherapy

28-day cycles

References

  1. van Wijk FH, Lhommé C, Bolis G, Scotto di Palumbo V, Tumolo S, Nooij M, Freire de Oliveira C, Vermorken JB; EORTC Gynaecological Cancer Group. Phase II study of carboplatin in patients with advanced or recurrent endometrial carcinoma: a trial of the EORTC Gynaecological Cancer Group. Eur J Cancer. 2003 Jan;39(1):78-85. link to original article contains dosing details in manuscript PubMed

Carboplatin & Paclitaxel (CP)

Regimen variant #1, 5/175, finite duration

Study Evidence
Pectasides et al. 2008 Phase 2

Chemotherapy

21-day cycle for 6 to 9 cycles


Regimen variant #2, 5/175, indefinite

Study Evidence
Hoskins et al. 2001 Phase 2
Sorbe et al. 2007 Phase 2

Note: this is the lower limit of carboplatin dosing allowed in Hoskins et al. 2001.

Chemotherapy

21-day cycles


Regimen variant #3, 6/175 x 7

ESMO-preferred (I-A, 2016)
Study Years of enrollment Evidence Comparator Comparative Efficacy
Miller et al. 2020 (GOG0209) 2003-2009 Phase 3 (E-de-esc) TAP Non-inferior OS
Median OS: 37 vs 41 mo
(HR 1.002, 90% CI 0.9-1.12)

Note: ESMO recommends 6 cycles, whereas the cited RCT uses 7 cycles.

Chemotherapy

21-day cycle for 7 cycles


Regimen variant #4, 6/175 x 6-10

Study Years of enrollment Evidence Comparator Comparative Efficacy
Powell et al. 2022 (GOG-0261) 2009-2014 Phase 3 (E-switch-ic) Ifosfamide & Paclitaxel Non-inferior OS
Median OS: 37 vs 29 mo
(HR 0.87, 90% CI 0.70-1.075)

Chemotherapy

21-day cycle for 6 to 10 cycles


Regimen variant #5, 7/175

Study Evidence
Hoskins et al. 2001 Phase 2

Note: this is the upper limit of carboplatin dosing allowed in Hoskins et al. 2001.

Chemotherapy

21-day cycles

References

  1. Hoskins PJ, Swenerton KD, Pike JA, Wong F, Lim P, Acquino-Parsons C, Lee N. Paclitaxel and carboplatin, alone or with irradiation, in advanced or recurrent endometrial cancer: a phase II study. J Clin Oncol. 2001 Oct 15;19(20):4048-53. link to original article contains dosing details in manuscript PubMed
  2. Sorbe B, Andersson H, Boman K, Rosenberg P, Kalling M. Treatment of primary advanced and recurrent endometrial carcinoma with a combination of carboplatin and paclitaxel-long-term follow-up. Int J Gynecol Cancer. 2008 Jul-Aug;18(4):803-8. Epub 2007 Oct 18. link to original article contains dosing details in manuscript PubMed
  3. Pectasides D, Xiros N, Papaxoinis G, Pectasides E, Sykiotis C, Koumarianou A, Psyrri A, Gaglia A, Kassanos D, Gouveris P, Panayiotidis J, Fountzilas G, Economopoulos T. Carboplatin and paclitaxel in advanced or metastatic endometrial cancer. Gynecol Oncol. 2008 May;109(2):250-4. Epub 2008 Mar 4. link to original article contains dosing details in manuscript PubMed content property of HemOnc.org
  4. Retrospective: Shechter-Maor G, Bruchim I, Ben-Harim Z, Altaras M, Fishman A. Combined chemotherapy regimen of carboplatin and paclitaxel as adjuvant treatment for papillary serous and clear cell endometrial cancer. Int J Gynecol Cancer. 2009 May;19(4):662-4. link to original article PubMed
  5. GOG0209: Miller DS, Filiaci VL, Mannel RS, Cohn DE, Matsumoto T, Tewari KS, DiSilvestro P, Pearl ML, Argenta PA, Powell MA, Zweizig SL, Warshal DP, Hanjani P, Carney ME, Huang H, Cella D, Zaino R, Fleming GF. Carboplatin and Paclitaxel for Advanced Endometrial Cancer: Final Overall Survival and Adverse Event Analysis of a Phase III Trial (NRG Oncology/GOG0209). J Clin Oncol. 2020 Nov 20;38(33):3841-3850. Epub 2020 Sep 29. link to original article contains dosing details in manuscript link to PMC article PubMed NCT00063999
  6. GOG-0261: Powell MA, Filiaci VL, Hensley ML, Huang HQ, Moore KN, Tewari KS, Copeland LJ, Secord AA, Mutch DG, Santin A, Warshal DP, Spirtos NM, DiSilvestro PA, Ioffe OB, Miller DS. Randomized Phase III Trial of Paclitaxel and Carboplatin Versus Paclitaxel and Ifosfamide in Patients With Carcinosarcoma of the Uterus or Ovary: An NRG Oncology Trial. J Clin Oncol. 2022 Mar 20;40(9):968-977. Epub 2022 Jan 10. link to original article contains dosing details in manuscript link to PMC article PubMed NCT00954174
  7. RUBY: NCT03981796

Carboplatin & Paclitaxel (CP) & Trastuzumab

CP+T: Carboplatin, Paclitaxel, Trastuzumab

Regimen

Study Years of enrollment Evidence Comparator Comparative Efficacy
Fader et al. 2018 2011-2017 Randomized Phase 2 (E-esc) CP Superior PFS1
Median PFS: 12.9 vs 8 mo
(HR 0.46, 90% CI 0.28-0.76)

1Reported efficacy is based on the 2020 update.

Biomarker eligibility criteria

  • HER2 overexpression

Chemotherapy

Targeted therapy

21-day cycles

References

  1. Fader AN, Roque DM, Siegel E, Buza N, Hui P, Abdelghany O, Chambers SK, Secord AA, Havrilesky L, O'Malley DM, Backes F, Nevadunsky N, Edraki B, Pikaart D, Lowery W, ElSahwi KS, Celano P, Bellone S, Azodi M, Litkouhi B, Ratner E, Silasi DA, Schwartz PE, Santin AD. Randomized Phase II Trial of Carboplatin-Paclitaxel Versus Carboplatin-Paclitaxel-Trastuzumab in Uterine Serous Carcinomas That Overexpress Human Epidermal Growth Factor Receptor 2/neu. J Clin Oncol. 2018 Jul 10;36(20):2044-2051. Epub 2018 Mar 27. link to original article contains dosing details in manuscript PubMed NCT01367002
    1. Update: Fader AN, Roque DM, Siegel E, Buza N, Hui P, Abdelghany O, Chambers S, Secord AA, Havrilesky L, O'Malley DM, Backes FJ, Nevadunsky N, Edraki B, Pikaart D, Lowery W, ElSahwi K, Celano P, Bellone S, Azodi M, Litkouhi B, Ratner E, Silasi DA, Schwartz PE, Santin AD. Randomized Phase II Trial of Carboplatin-Paclitaxel Compared with Carboplatin-Paclitaxel-Trastuzumab in Advanced (Stage III-IV) or Recurrent Uterine Serous Carcinomas that Overexpress Her2/Neu (NCT01367002): Updated Overall Survival Analysis. Clin Cancer Res. 2020 Aug 1;26(15):3928-3935. Epub 2020 Jun 29. link to original article link to PMC article PubMed

Carboplatin & Pegylated liposomal doxorubicin

Regimen

Study Evidence
Pignata et al. 2007 (END-1) Phase 2

Note: All patients received 3 cycles of therapy. If there was no unacceptable toxicity, patients with stable or responsive disease received an additional 3 cycles.

Chemotherapy

Supportive therapy

  • G-CSF by the following criteria:
    • Prophylaxis: not recommended
    • Grade 4 neutropenia: therapeutic and prophylactic use was allowed

28-day cycle for 3 to 6 cycles

References

  1. END-1: Pignata S, Scambia G, Pisano C, Breda E, Di Maio M, Greggi S, Ferrandina G, Lorusso D, Zagonel V, Febbraro A, Riva N, De Rosa V, Gallo C, Perrone F; Multicentre Italian Trials in Ovarian Cancer and Gynecologic Malignancies Group. A multicentre phase II study of carboplatin plus pegylated liposomal doxorubicin as first-line chemotherapy for patients with advanced or recurrent endometrial carcinoma: the END-1 study of the MITO (Multicentre Italian Trials in Ovarian Cancer and Gynecologic Malignancies) group. Br J Cancer. 2007 Jun 4;96(11):1639-43. Epub 2007 May 8. link to original article contains dosing details in manuscript link to PMC article PubMed

CIM

CIM: Cisplatin, Ifosfamide, Mesna

Regimen

Study Years of enrollment Evidence Comparator Comparative Efficacy
Sutton et al. 2000 (GOG 108) 1989-1996 Phase 3 (E-esc) Ifosfamide Seems to have superior PFS

Chemotherapy

Supportive therapy

References

  1. GOG 108: Sutton G, Brunetto VL, Kilgore L, Soper JT, McGehee R, Olt G, Lentz SS, Sorosky J, Hsiu JG. A phase III trial of ifosfamide with or without cisplatin in carcinosarcoma of the uterus: A Gynecologic Oncology Group study. Gynecol Oncol. 2000 Nov;79(2):147-53. link to original article PubMed

Cisplatin & Doxorubicin

AP: Adriamycin (Doxorubicin) & Platinol (Cisplatin)

Regimen variant #1, 50/45

Study Years of enrollment Evidence Comparator Comparative Efficacy
Fleming et al. 2004a (GOG 177) 1998-2000 Phase 3 (C) Cisplatin, Doxorubicin, Paclitaxel Seems to have inferior OS

Note: body surface area was capped at 2 m2. This dosage was for patients with previous pelvic radiation or who were greater than 65 years old.

Chemotherapy

21-day cycle for 7 cycles


Regimen variant #2, 50/60, capped BSA

Study Years of enrollment Evidence Comparator Comparative Efficacy
Fleming et al. 2004a (GOG 177) 1998-2000 Phase 3 (C) Cisplatin, Doxorubicin, Paclitaxel Seems to have inferior OS

Note: body surface area was capped at 2 m2.

Chemotherapy

21-day cycle for 7 cycles


Regimen variant #3, 50/60, no cap on BSA

Study Years of enrollment Evidence Comparator Comparative Efficacy
Fleming et al. 2004 (GOG 163) 1996-1998 Phase 3 (C) Doxorubicin & Paclitaxel Did not meet primary endpoint of ORR
Thigpen et al. 2004 (GOG 107) NR Phase 3 (E-esc) Doxorubicin Seems to have superior PFS

Chemotherapy

Supportive therapy

21-day cycle for up to 8 cycles


Regimen variant #4, 60/60

Study Years of enrollment Evidence Comparator Comparative Efficacy
Gallion et al. 2003 (GOG 139) 1993-1996 Phase 3 (C) Cisplatin & Doxorubicin; chronomodulated Did not meet primary endpoint of ORR

Chemotherapy

21-day cycle for up to 8 cycles

References

  1. GOG 139: Gallion HH, Brunetto VL, Cibull M, Lentz SS, Reid G, Soper JT, Burger RA, Andersen W; Gynecologic Oncology Group. Randomized phase III trial of standard timed doxorubicin plus cisplatin versus circadian timed doxorubicin plus cisplatin in stage III and IV or recurrent endometrial carcinoma: a Gynecologic Oncology Group study. J Clin Oncol. 2003 Oct 15;21(20):3808-13. link to original article contains dosing details in abstract PubMed
  2. GOG 177: Fleming GF, Brunetto VL, Cella D, Look KY, Reid GC, Munkarah AR, Kline R, Burger RA, Goodman A, Burks RT. Phase III trial of doxorubicin plus cisplatin with or without paclitaxel plus filgrastim in advanced endometrial carcinoma: a Gynecologic Oncology Group study. J Clin Oncol. 2004 Jun 1;22(11):2159-66. link to original article contains dosing details in manuscript PubMed NCT00003691
  3. GOG 163: Fleming GF, Filiaci VL, Bentley RC, Herzog T, Sorosky J, Vaccarello L, Gallion H. Phase III randomized trial of doxorubicin + cisplatin versus doxorubicin + 24-h paclitaxel + filgrastim in endometrial carcinoma: a Gynecologic Oncology Group study. Ann Oncol. 2004 Aug;15(8):1173-8. link to original article contains dosing details in abstract PubMed
  4. GOG 107: Thigpen JT, Brady MF, Homesley HD, Malfetano J, DuBeshter B, Burger RA, Liao S. Phase III trial of doxorubicin with or without cisplatin in advanced endometrial carcinoma: a Gynecologic Oncology Group study. J Clin Oncol. 2004 Oct 1;22(19):3902-8. link to original article contains dosing details in abstract PubMed

Cisplatin, Doxorubicin, Paclitaxel

TAP: Taxol (Paclitaxel), Adriamycin (Doxorubicin), Platinol (Cisplatin)
CDP: Cisplatin, Doxorubicin, Paclitaxel

Regimen

Study Years of enrollment Evidence Comparator Comparative Efficacy
Fleming et al. 2004 (GOG 177) 1998-2000 Phase 3 (E-esc) Cisplatin & Doxorubicin Seems to have superior OS
Median OS: 15.3 vs 12.3 mo
(HR 0.75, 95% CI 0.57-0.99)
Miller et al. 2020 (GOG0209) 2003-2009 Phase 3 (C) TC Non-inferior OS

Note: in GOG 177, body surface area was capped at 2 m2.

Chemotherapy

Supportive therapy

21-day cycle for 7 cycles

References

  1. GOG 177: Fleming GF, Brunetto VL, Cella D, Look KY, Reid GC, Munkarah AR, Kline R, Burger RA, Goodman A, Burks RT. Phase III trial of doxorubicin plus cisplatin with or without paclitaxel plus filgrastim in advanced endometrial carcinoma: a Gynecologic Oncology Group study. J Clin Oncol. 2004 Jun 1;22(11):2159-66. link to original article contains dosing details in manuscript PubMed NCT00003691
  2. GOG0209: Miller DS, Filiaci VL, Mannel RS, Cohn DE, Matsumoto T, Tewari KS, DiSilvestro P, Pearl ML, Argenta PA, Powell MA, Zweizig SL, Warshal DP, Hanjani P, Carney ME, Huang H, Cella D, Zaino R, Fleming GF. Carboplatin and Paclitaxel for Advanced Endometrial Cancer: Final Overall Survival and Adverse Event Analysis of a Phase III Trial (NRG Oncology/GOG0209). J Clin Oncol. 2020 Nov 20;38(33):3841-3850. Epub 2020 Sep 29. link to original article contains dosing details in manuscript link to PMC article PubMed NCT00063999

Cisplatin & Paclitaxel

Regimen

Study Evidence
Dimopoulos et al. 2000 Phase 2

Chemotherapy

Supportive therapy

21-day cycle for up to 6 cycles

References

  1. Dimopoulos MA, Papadimitriou CA, Georgoulias V, Moulopoulos LA, Aravantinos G, Gika D, Karpathios S, Stamatelopoulos S. Paclitaxel and cisplatin in advanced or recurrent carcinoma of the endometrium: long-term results of a phase II multicenter study. Gynecol Oncol. 2000 Jul;78(1):52-7. link to original article contains dosing details in manuscript PubMed

Dactinomycin monotherapy

Regimen

Study Evidence
Moore et al. 1999 Phase 2

Chemotherapy

28-day cycles

References

  1. Moore DH, Blessing JA, Dunton C, Buller RE, Reid GC; Gynecologic Oncology Group. Dactinomycin in the treatment of recurrent or persistent endometrial carcinoma: A Phase II study of the Gynecologic Oncology Group. Gynecol Oncol. 1999 Dec;75(3):473-5. link to original article contains dosing details in manuscript PubMed

Dostarlimab monotherapy

Regimen

FDA-recommended dose
Study Years of enrollment Evidence
Oaknin et al. 2020 (GARNET) 2017-2019 Phase 1, >20 pts in this cohort (RT)

Immunotherapy

  • Dostarlimab (Jemperli) as follows:
    • Cycles 1 to 4: 500 mg IV over 30 minutes once on day 1
    • Cycle 5 onwards: 1000 mg IV over 30 minutes once on day 1

21-day cycle for 4 cycles, then 42-day cycles

References

  1. GARNET: Oaknin A, Tinker AV, Gilbert L, Samouëlian V, Mathews C, Brown J, Barretina-Ginesta MP, Moreno V, Gravina A, Abdeddaim C, Banerjee S, Guo W, Danaee H, Im E, Sabatier R. Clinical Activity and Safety of the Anti-Programmed Death 1 Monoclonal Antibody Dostarlimab for Patients With Recurrent or Advanced Mismatch Repair-Deficient Endometrial Cancer: A Nonrandomized Phase 1 Clinical Trial. JAMA Oncol. 2020 Nov 1;6(11):1766-1772. Epub 2020 Oct 1. link to original article link to PMC article contains dosing details in manuscript PubMed NCT02715284
    1. Update: Oaknin A, Gilbert L, Tinker AV, Brown J, Mathews C, Press J, Sabatier R, O'Malley DM, Samouelian V, Boni V, Duska L, Ghamande S, Ghatage P, Kristeleit R, Leath C III, Guo W, Im E, Zildjian S, Han X, Duan T, Veneris J, Pothuri B. Safety and antitumor activity of dostarlimab in patients with advanced or recurrent DNA mismatch repair deficient/microsatellite instability-high (dMMR/MSI-H) or proficient/stable (MMRp/MSS) endometrial cancer: interim results from GARNET-a phase I, single-arm study. J Immunother Cancer. 2022 Jan;10(1):e003777. link to original article link to PMC article PubMed

Doxorubicin monotherapy

Regimen variant #1, 7 cycles

Study Years of enrollment Evidence Comparator Comparative Efficacy
Aapro et al. 2003 (EORTC 55872) 1988-1994 Phase 3 (C) Cisplatin & Doxorubicin Might have inferior OS

Note: to our knowledge, this regimen was not tested as an experimental arm in an RCT in this context, prior to becoming a standard comparator arm.

Chemotherapy

28-day cycle for up to 7 cycles


Regimen variant #2, 8 cycles

Study Years of enrollment Evidence Comparator Comparative Efficacy
Thigpen et al. 1979 NR Phase 2
Omura et al. 1983 (GOG 21) 1973-1979 Randomized (C) Dacarbazine & Doxorubicin Did not meet primary endpoint of ORR
Muss et al. 1985 (GOG 42) 1979-1982 Phase 3 (C) Cyclophosphamide & Doxorubicin (AC) Did not meet efficacy endpoints
Thigpen et al. 1994 (GOG 48) 1979-1985 Randomized (C) Cyclophosphamide & Doxorubicin (AC) Did not meet efficacy endpoints
Thigpen et al. 2004 (GOG 107) NR Phase 3 (C) Cisplatin & Doxorubicin Seems to have inferior PFS
Makker et al. 2022 (KEYNOTE-775) 2018-2020 Phase 3 (C) Lenvatinib & Pembrolizumab Inferior OS

Note: to our knowledge, this regimen was not tested as an experimental arm in an RCT in this context, prior to becoming a standard comparator arm.

Chemotherapy

21-day cycle for up to 8 cycles

References

  1. Thigpen JT, Buchsbaum HJ, Mangan C, Blessing JA; Gynecologic Oncology Group. Phase II trial of adriamycin in the treatment of advanced or recurrent endometrial carcinoma: a Gynecologic Oncology Group study. Cancer Treat Rep. 1979 Jan;63(1):21-7. PubMed
  2. GOG 21: Omura GA, Major FJ, Blessing JA, Sedlacek TV, Thigpen JT, Creasman WT, Zaino RJ. A randomized study of adriamycin with and without dimethyl triazenoimidazole carboxamide in advanced uterine sarcomas. Cancer. 1983 Aug 15;52(4):626-32. link to original article PubMed
  3. GOG 42: Muss HB, Bundy B, DiSaia PJ, Homesley HD, Fowler WC Jr, Creasman W, Yordan E. Treatment of recurrent or advanced uterine sarcoma: a randomized trial of doxorubicin versus doxorubicin and cyclophosphamide (a phase III trial of the Gynecologic Oncology Group). Cancer. 1985 Apr 15;55(8):1648-53. link to original article PubMed
  4. GOG 48: Thigpen JT, Blessing JA, DiSaia PJ, Yordan E, Carson LF, Evers C. A randomized comparison of doxorubicin alone versus doxorubicin plus cyclophosphamide in the management of advanced or recurrent endometrial carcinoma: a Gynecologic Oncology Group study. J Clin Oncol. 1994 Jul;12(7):1408-14. link to original article contains dosing details in abstract PubMed
  5. EORTC 55872: Aapro MS, van Wijk FH, Bolis G, Chevallier B, van der Burg ME, Poveda A, Freire de Oliveira C, Tumolo S, Scotto di Palumbo V, Piccart M, Franchi M, Zanaboni F, Lacave AJ, Fontanelli R, Favalli G, Zola P, Guastalla JP, Rosso R, Marth C, Nooij M, Presti M, Scarabelli C, Splinter TA, Ploch E, Beex LV, ten Bokkel Huinink W, Forni M, Melpignano M, Blake P, Kerbrat P, Mendiola C, Cervantes A, Goupil A, Harper PG, Madronal C, Namer M, Scarfone G, Stoot JE, Teodorovic I, Coens C, Vergote I, Vermorken JB; EORTC Gynaecological Cancer Group. Doxorubicin versus doxorubicin and cisplatin in endometrial carcinoma: definitive results of a randomised study (55872) by the EORTC Gynaecological Cancer Group. Ann Oncol. 2003 Mar;14(3):441-8. Erratum in: Ann Oncol. 2003 May;14(5):811. link to original article contains dosing details in manuscript PubMed
  6. GOG 107: Thigpen JT, Brady MF, Homesley HD, Malfetano J, DuBeshter B, Burger RA, Liao S. Phase III trial of doxorubicin with or without cisplatin in advanced endometrial carcinoma: a Gynecologic Oncology Group study. J Clin Oncol. 2004 Oct 1;22(19):3902-8. link to original article contains dosing details in abstract PubMed
  7. KEYNOTE-775: Makker V, Colombo N, Casado Herráez A, Santin AD, Colomba E, Miller DS, Fujiwara K, Pignata S, Baron-Hay S, Ray-Coquard I, Shapira-Frommer R, Ushijima K, Sakata J, Yonemori K, Kim YM, Guerra EM, Sanli UA, McCormack MM, Smith AD, Keefe S, Bird S, Dutta L, Orlowski RJ, Lorusso D; Study 309–KEYNOTE-775 Investigators. Lenvatinib plus Pembrolizumab for Advanced Endometrial Cancer. N Engl J Med. 2022 Feb 3;386(5):437-448. Epub 2022 Jan 19. link to original article contains dosing details in manuscript PubMed NCT03517449

Ifosfamide monotherapy

Regimen variant #1, 1200 mg/m2 (3 days/cycle)

Study Years of enrollment Evidence Comparator Comparative Efficacy
Homesley et al. 2007 (GOG 161) 1997-2004 Phase 3 (C) Ifosfamide & Paclitaxel Seems to have inferior OS

Note: GOG 161 specifies that PO Mesna (Mesnex) is to be taken in 3 divided doses, but only lists 2 time points for its use. The timing of the middle dose is estimated based on other references. This dosage is intended for patients with previous radiation.

Chemotherapy

Supportive therapy

  • Mesna (Mesnex) 2000 mg IV over 12 hours once per day on days 1 to 3, starting 15 minutes before Ifosfamide (Ifex) (total dose per cycle: 6000 mg/m2)
    • Alternate PO dosing: 1330 mg PO three times per day on days 1 to 3, taken 1 hour before, 4 hours after, and 8 hours after Ifosfamide (Ifex) (total dose per cycle: 11,970 mg)
  • Filgrastim (Neupogen) 5 mcg/kg SC once per day, starting on day 4, to continue until ANC is greater than or equal to 2000/uL

21-day cycle for 8 cycles


Regimen variant #2, 1500 mg/m2 (5 days/cycle)

Study Years of enrollment Evidence Comparator Comparative Efficacy
Sutton et al. 2000 (GOG 108) 1989-1996 Phase 3 (C) CIM Seems to have inferior PFS

Chemotherapy

Supportive therapy

21-day cycle for 8 cycles


Regimen variant #3, 1600 mg/m2 (3 days/cycle)

Study Years of enrollment Evidence Comparator Comparative Efficacy
Homesley et al. 2007 (GOG 161) 1997-2004 Phase 3 (C) Ifosfamide & Paclitaxel Seems to have inferior OS

Note: GOG 161 specifies that PO Mesna (Mesnex) is to be taken in 3 divided doses, but only lists 2 time points for its use. The timing of the middle dose is estimated based on other references.

Chemotherapy

  • Ifosfamide (Ifex) 1600 mg/m2 IV once per day on days 1 to 3
    • Dosage for patients with previous radiation: 1200 mg/m2 IV once per day on days 1 to 3

Supportive therapy

  • Mesna (Mesnex) 2000 mg IV over 12 hours once per day on days 1 to 3, starting 15 minutes before Ifosfamide (Ifex) (total dose per cycle: 6000 mg/m2)
    • Alternate PO dosing: 1330 mg PO three times per day on days 1 to 3, taken 1 hour before, 4 hours after, and 8 hours after Ifosfamide (Ifex) (total dose per cycle: 11,970 mg)
  • Filgrastim (Neupogen) 5 mcg/kg SC once per day, starting on day 4, to continue until ANC is greater than or equal to 2000/uL

21-day cycle for 8 cycles

References

  1. GOG 108: Sutton G, Brunetto VL, Kilgore L, Soper JT, McGehee R, Olt G, Lentz SS, Sorosky J, Hsiu JG. A phase III trial of ifosfamide with or without cisplatin in carcinosarcoma of the uterus: A Gynecologic Oncology Group study. Gynecol Oncol. 2000 Nov;79(2):147-53. link to original article contains dosing details in manuscript PubMed
  2. GOG 161: Homesley HD, Filiaci V, Markman M, Bitterman P, Eaton L, Kilgore LC, Monk BJ, Ueland FR; Gynecologic Oncology Group. Phase III trial of ifosfamide with or without paclitaxel in advanced uterine carcinosarcoma: a Gynecologic Oncology Group study. J Clin Oncol. 2007 Feb 10;25(5):526-31. link to original article contains dosing details in manuscript PubMed NCT00003128

Ifosfamide & Paclitaxel

PI: Paclitaxel & Ifosfamide

Regimen

Study Years of enrollment Evidence Comparator Comparative Efficacy
Homesley et al. 2007 (GOG 161) 1997-2004 Phase 3 (E-esc) Ifosfamide Seems to have superior OS
Median OS: 13.5 vs 8.4 mo
(HR 0.69, 95% CI 0.49-0.97)
Powell et al. 2022 (GOG-0261) 2009-2014 Phase 3 (C) Carboplatin & Paclitaxel Non-inferior OS

Note: GOG 161 specifies that PO Mesna (Mesnex) is to be taken in 3 divided doses, but only lists 2 time points for its use. The timing of the middle dose is estimated based on other references. Treatment was given for 8 cycles in GOG 161.

Chemotherapy

  • Ifosfamide (Ifex) by the following criteria:
    • No previous radiation: 1600 mg/m2 IV once per day on days 1 to 3
    • Previous radiation: 1200 mg/m2 IV once per day on days 1 to 3
  • Paclitaxel (Taxol) 135 mg/m2 IV over 3 hours once on day 1

Supportive therapy

Per GOG 161:

21-day cycle for 6 to 10 cycles

References

  1. GOG 161: Homesley HD, Filiaci V, Markman M, Bitterman P, Eaton L, Kilgore LC, Monk BJ, Ueland FR; Gynecologic Oncology Group. Phase III trial of ifosfamide with or without paclitaxel in advanced uterine carcinosarcoma: a Gynecologic Oncology Group study. J Clin Oncol. 2007 Feb 10;25(5):526-31. link to original article contains dosing details in manuscript PubMed NCT00003128
  2. GOG-0261: Powell MA, Filiaci VL, Hensley ML, Huang HQ, Moore KN, Tewari KS, Copeland LJ, Secord AA, Mutch DG, Santin A, Warshal DP, Spirtos NM, DiSilvestro PA, Ioffe OB, Miller DS. Randomized Phase III Trial of Paclitaxel and Carboplatin Versus Paclitaxel and Ifosfamide in Patients With Carcinosarcoma of the Uterus or Ovary: An NRG Oncology Trial. J Clin Oncol. 2022 Mar 20;40(9):968-977. Epub 2022 Jan 10. link to original article contains dosing details in manuscript link to PMC article PubMed NCT00954174

Lenvatinib & Pembrolizumab

Regimen

Study Years of enrollment Evidence Comparator Comparative Efficacy
Makker et al. 2019 (KEYNOTE-146) 2015-2017 Phase 2 (RT)
Makker et al. 2022 (KEYNOTE-775) 2018-2020 Phase 3 (E-RT-switch-ooc) 1. Doxorubicin
2. Paclitaxel
Superior OS1
Median OS: 18.3 vs 11.4 mo
(HR 0.62, 95% CI 0.51-0.75)

1Reported efficacy is for the overall population.

Targeted therapy

Immunotherapy

21-day cycles

References

  1. KEYNOTE-146: Makker V, Rasco D, Vogelzang NJ, Brose MS, Cohn AL, Mier J, Di Simone C, Hyman DM, Stepan DE, Dutcus CE, Schmidt EV, Guo M, Sachdev P, Shumaker R, Aghajanian C, Taylor M. Lenvatinib plus pembrolizumab in patients with advanced endometrial cancer: an interim analysis of a multicentre, open-label, single-arm, phase 2 trial. Lancet Oncol. 2019 May;20(5):711-718. Epub 2019 Mar 25. link to original article contains dosing details in abstract PubMed NCT02501096
    1. Update: Makker V, Taylor MH, Aghajanian C, Oaknin A, Mier J, Cohn AL, Romeo M, Bratos R, Brose MS, DiSimone C, Messing M, Stepan DE, Dutcus CE, Wu J, Schmidt EV, Orlowski R, Sachdev P, Shumaker R, Casado Herraez A. Lenvatinib Plus Pembrolizumab in Patients With Advanced Endometrial Cancer. J Clin Oncol. 2020 Sep 10;38(26):2981-2992. Epub 2020 Mar 13. link to original article link to PMC article PubMed
  2. KEYNOTE-775: Makker V, Colombo N, Casado Herráez A, Santin AD, Colomba E, Miller DS, Fujiwara K, Pignata S, Baron-Hay S, Ray-Coquard I, Shapira-Frommer R, Ushijima K, Sakata J, Yonemori K, Kim YM, Guerra EM, Sanli UA, McCormack MM, Smith AD, Keefe S, Bird S, Dutta L, Orlowski RJ, Lorusso D; Study 309–KEYNOTE-775 Investigators. Lenvatinib plus Pembrolizumab for Advanced Endometrial Cancer. N Engl J Med. 2022 Feb 3;386(5):437-448. Epub 2022 Jan 19. link to original article contains dosing details in manuscript PubMed NCT03517449

Paclitaxel monotherapy

Regimen variant #1, 80 mg/m2

Study Years of enrollment Evidence Comparator Comparative Efficacy
Makker et al. 2022 (KEYNOTE-775) 2018-2020 Phase 3 (C) Lenvatinib & Pembrolizumab Inferior OS

Note: to our knowledge, this regimen was not tested as an experimental arm in an RCT in this context, prior to becoming a standard comparator arm.

Chemotherapy

28-day cycles


Regimen variant #2, 175 mg/m2

Study Years of enrollment Evidence Comparator Comparative Efficacy
Lissoni et al. 1996 1993-1995 Phase 2
Lincoln et al. 2003 1994-1996 Phase 2
McMeekin et al. 2015 (IXAMPLE2) 2009-2012 Phase 3 (C) Ixabepilone Seems to have superior OS

Note: in Lincoln et al. 2003, this was the dosage for patients with previous pelvic radiation.

Chemotherapy

Supportive therapy

21-day cycles


Regimen variant #3, 200 mg/m2

Study Years of enrollment Evidence
Ball et al. 1996 NR in abstract Phase 2
Lincoln et al. 2003 1994-1996 Phase 2

Note: in Ball et al. 1996, this was the dosage for patients with previous pelvic radiation.

Chemotherapy

  • Paclitaxel (Taxol) 200 mg/m2 IV over 3 hours once on day 1
    • Ball et al. 1996 gave as a 24 hour continuous infusion
    • Dose can be changed to 135 or 110 mg/m2 depending on toxicity

Supportive therapy

21-day cycles


Regimen variant #4, 250 mg/m2

Study Evidence
Ball et al. 1996 Phase 2

Chemotherapy

  • Paclitaxel (Taxol) 250 mg/m2 IV continuous infusion over 24 hours, started on day 1
    • Dosage for patients with previous pelvic radiation: 200 mg/m2 IV continuous infusion over 24 hours, started on day 1
    • Dose can be changed to 200, 170, 135, 110 mg/m2 depending on toxicity

Supportive therapy

21-day cycles

References

  1. Ball HG, Blessing JA, Lentz SS, Mutch DG; Gynecologic Oncology Group. A phase II trial of paclitaxel in patients with advanced or recurrent adenocarcinoma of the endometrium: a Gynecologic Oncology Group study. Gynecol Oncol. 1996 Aug;62(2):278-81. link to original article contains dosing details in manuscript PubMed
  2. Lissoni A, Zanetta G, Losa G, Gabriele A, Parma G, Mangioni C. Phase II study of paclitaxel as salvage treatment in advanced endometrial cancer. Ann Oncol. 1996 Oct;7(8):861-3. link to original article contains dosing details in manuscript PubMed
  3. Lincoln S, Blessing JA, Lee RB, Rocereto TF; Gynecologic Oncology Group. Activity of paclitaxel as second-line chemotherapy in endometrial carcinoma: a Gynecologic Oncology Group study. Gynecol Oncol. 2003 Mar;88(3):277-81. link to original article contains dosing details in manuscript PubMed
  4. IXAMPLE2: McMeekin S, Dizon D, Barter J, Scambia G, Manzyuk L, Lisyanskaya A, Oaknin A, Ringuette S, Mukhopadhyay P, Rosenberg J, Vergote I. Phase III randomized trial of second-line ixabepilone versus paclitaxel or doxorubicin in women with advanced endometrial cancer. Gynecol Oncol. 2015 Jul;138(1):18-23. Epub 2015 Apr 26. link to original article contains dosing details in abstract PubMed NCT00883116
  5. KEYNOTE-775: Makker V, Colombo N, Casado Herráez A, Santin AD, Colomba E, Miller DS, Fujiwara K, Pignata S, Baron-Hay S, Ray-Coquard I, Shapira-Frommer R, Ushijima K, Sakata J, Yonemori K, Kim YM, Guerra EM, Sanli UA, McCormack MM, Smith AD, Keefe S, Bird S, Dutta L, Orlowski RJ, Lorusso D; Study 309–KEYNOTE-775 Investigators. Lenvatinib plus Pembrolizumab for Advanced Endometrial Cancer. N Engl J Med. 2022 Feb 3;386(5):437-448. Epub 2022 Jan 19. link to original article contains dosing details in manuscript PubMed NCT03517449

Pembrolizumab monotherapy

Regimen variant #1, bi-weekly

Study Years of enrollment Evidence
Le et al. 2015 (KEYNOTE-016) 2013-2016 Phase 2, <20 pts of this subtype
Ott et al. 2017b (KEYNOTE-028) NR Phase 1b

Note: KEYNOTE-016 was an expansion to a CRC-specific trial.

Immunotherapy

14-day cycle for up to 52 cycles (2 years)


Regimen variant #2, q3wk

Study Years of enrollment Evidence
O'Malley et al. 2022 (KEYNOTE-158) 2016-2020 Phase 2 (RT)

Biomarker eligibility criteria

  • Cohort K: MSI-H/dMMR endometrial cancer

Immunotherapy

21-day cycle for up to 35 cycles (2 years)

References

  1. KEYNOTE-028: Ott PA, Bang YJ, Berton-Rigaud D, Elez E, Pishvaian MJ, Rugo HS, Puzanov I, Mehnert JM, Aung KL, Lopez J, Carrigan M, Saraf S, Chen M, Soria JC. Safety and antitumor activity of pembrolizumab in advanced programmed death ligand 1-positive endometrial cancer: results from the KEYNOTE-028 study. J Clin Oncol. 2017 Aug 1;35(22):2535-2541. Epub 2017 May 10. link to original article contains dosing details in abstract PubMed NCT02054806
  2. KEYNOTE-016: Le DT, Uram JN, Wang H, Bartlett BR, Kemberling H, Eyring AD, Skora AD, Luber BS, Azad NS, Laheru D, Biedrzycki B, Donehower RC, Zaheer A, Fisher GA, Crocenzi TS, Lee JJ, Duffy SM, Goldberg RM, de la Chapelle A, Koshiji M, Bhaijee F, Huebner T, Hruban RH, Wood LD, Cuka N, Pardoll DM, Papadopoulos N, Kinzler KW, Zhou S, Cornish TC, Taube JM, Anders RA, Eshleman JR, Vogelstein B, Diaz LA Jr. PD-1 blockade in tumors with mismatch-repair deficiency. N Engl J Med. 2015 Jun 25;372(26):2509-20. Epub 2015 May 30. link to original article contains dosing details in abstract link to PMC article PubMed NCT01876511
    1. Update: Le DT, Durham JN, Smith KN, Wang H, Bartlett BR, Aulakh LK, Lu S, Kemberling H, Wilt C, Luber BS, Wong F, Azad NS, Rucki AA, Laheru D, Donehower R, Zaheer A, Fisher GA, Crocenzi TS, Lee JJ, Greten TF, Duffy AG, Ciombor KK, Eyring AD, Lam BH, Joe A, Kang SP, Holdhoff M, Danilova L, Cope L, Meyer C, Zhou S, Goldberg RM, Armstrong DK, Bever KM, Fader AN, Taube J, Housseau F, Spetzler D, Xiao N, Pardoll DM, Papadopoulos N, Kinzler KW, Eshleman JR, Vogelstein B, Anders RA, Diaz LA Jr. Mismatch repair deficiency predicts response of solid tumors to PD-1 blockade. Science. 2017 Jul 28;357(6349):409-413. Epub 2017 Jun 8. link to original article link to PMC article contains dosing details in supplement PubMed
  3. KEYNOTE-158: O'Malley DM, Bariani GM, Cassier PA, Marabelle A, Hansen AR, De Jesus Acosta A, Miller WH Jr, Safra T, Italiano A, Mileshkin L, Xu L, Jin F, Norwood K, Maio M. Pembrolizumab in Patients With Microsatellite Instability-High Advanced Endometrial Cancer: Results From the KEYNOTE-158 Study. J Clin Oncol. 2022 Mar 1;40(7):752-761. Epub 2022 Jan 6. link to original article link to PMC article contains dosing details in abstract PubMed NCT02628067

Temsirolimus monotherapy

Regimen

Study Evidence
Oza et al. 2011 (NCIC IND.160) Phase 2

Targeted therapy

28-day cycles

References

  1. NCIC IND.160: Oza AM, Elit L, Tsao MS, Kamel-Reid S, Biagi J, Provencher DM, Gotlieb WH, Hoskins PJ, Ghatage P, Tonkin KS, Mackay HJ, Mazurka J, Sederias J, Ivy P, Dancey JE, Eisenhauer EA; NCIC Clinical Trials Group. Phase II study of temsirolimus in women with recurrent or metastatic endometrial cancer: a trial of the NCIC Clinical Trials Group. J Clin Oncol. 2011 Aug 20;29(24):3278-85. Epub 2011 Jul 25. link to original article contains dosing details in manuscript link to PMC article PubMed NCT00072176

Topotecan monotherapy

Regimen

Study Evidence
Wadler et al. 2003 (ECOG E3E93) Phase 2

Chemotherapy

  • Topotecan (Hycamtin) 1.5 mg/m2 IV once per day on days 1 to 5
    • Dosage for patients with previous pelvic radiation: 1.2 mg/m2, which can be increased to the 1.5 mg/m2 dose in later cycles if there are no toxicities higher than grade 1

21-day cycles

References

  1. ECOG E3E93: Wadler S, Levy DE, Lincoln ST, Soori GS, Schink JC, Goldberg G. Topotecan is an active agent in the first-line treatment of metastatic or recurrent endometrial carcinoma: Eastern Cooperative Oncology Group Study E3E93. J Clin Oncol. 2003 Jun 1;21(11):2110-4. link to original article contains dosing details in manuscript PubMed

Endocrine therapy for advanced, recurrent, or metastatic disease

Anastrozole monotherapy

Regimen

Study Evidence
Rose et al. 2000 Phase 2

Endocrine therapy

Continued indefinitely

References

  1. Rose PG, Brunetto VL, VanLe L, Bell J, Walker JL, Lee RB; Gynecologic Oncology Group. A phase II trial of anastrozole in advanced recurrent or persistent endometrial carcinoma: a Gynecologic Oncology Group study. Gynecol Oncol. 2000 Aug;78(2):212-6. link to original article contains dosing details in manuscript PubMed

Medroxyprogesterone monotherapy

Regimen

Study Years of enrollment Evidence Comparator Comparative Efficacy
Kelley & Baker 1961 1950-1959 Non-randomized
Thigpen et al. 1999 1985-1989 Phase 3 (C) Medroxyprogesterone; high-dose Did not meet primary endpoint of ORR

Note: to our knowledge, this regimen was not tested as an experimental arm in an RCT in this context, prior to becoming a standard comparator arm. Kelley & Baker 1961 examined a variety of progestins and is included for historic interest.

Endocrine therapy

Continued indefinitely

References

  1. Kelley RM, Baker WH. Progestational agents in the treatment of carcinoma of the endometrium. N Engl J Med. 1961 Feb 2;264:216-22. link to original article PubMed
  2. Thigpen JT, Brady MF, Alvarez RD, Adelson MD, Homesley HD, Manetta A, Soper JT, Given FT; Gynecologic Oncology Group. Oral medroxyprogesterone acetate in the treatment of advanced or recurrent endometrial carcinoma: a dose-response study by the Gynecologic Oncology Group. J Clin Oncol. 1999 Jun;17(6):1736-44. link to original article contains dosing details in manuscript PubMed

Medroxyprogesterone & Tamoxifen

Regimen

Study Evidence
Whitney et al. 2004 Phase 2

Endocrine therapy

Continued indefinitely

References

  1. Whitney CW, Brunetto VL, Zaino RJ, Lentz SS, Sorosky J, Armstrong DK, Lee RB; Gynecologic Oncology Group. Phase II study of medroxyprogesterone acetate plus tamoxifen in advanced endometrial carcinoma: a Gynecologic Oncology Group study. Gynecol Oncol. 2004 Jan;92(1):4-9. link to original article contains dosing details in manuscript PubMed

Megestrol monotherapy

Regimen

Study Years of enrollment Evidence Comparator Comparative Efficacy
Kelley & Baker 1961 1950-1959 Non-randomized
Pandya et al. 2001 (ECOG E4882) 1982-1984 Randomized Phase 2 (C) Megestrol & Tamoxifen Did not meet efficacy endpoints

Note: to our knowledge, this regimen was not tested as an experimental arm in an RCT in this context, prior to becoming a standard comparator arm. Kelley & Baker 1961 examined a variety of progestins and is included for historic interest.

Endocrine therapy

Continued indefinitely

References

  1. Kelley RM, Baker WH. Progestational agents in the treatment of carcinoma of the endometrium. N Engl J Med. 1961 Feb 2;264:216-22. link to original article PubMed
  2. ECOG E4882: Pandya KJ, Yeap BY, Weiner LM, Krook JE, Erban JK, Schinella RA, Davis TE. Megestrol and tamoxifen in patients with advanced endometrial cancer: an Eastern Cooperative Oncology Group Study (E4882). Am J Clin Oncol. 2001 Feb;24(1):43-6. link to original article contains dosing details in manuscript PubMed

Megestrol & Tamoxifen

Regimen

Study Years of enrollment Evidence Comparator Comparative Efficacy
Pandya et al. 2001 (ECOG E4882) 1982-1984 Randomized Phase 2 (E-switch-ic) Megestrol Did not meet primary efficacy endpoints
Fiorica et al. 2004 1994-1995 Phase 2

Endocrine therapy, part 1

21-day cycles, alternating with tamoxifen

Endocrine therapy, part 2

21-day cycles, alternating with megestrol

References

  1. ECOG E4882: Pandya KJ, Yeap BY, Weiner LM, Krook JE, Erban JK, Schinella RA, Davis TE. Megestrol and tamoxifen in patients with advanced endometrial cancer: an Eastern Cooperative Oncology Group Study (E4882). Am J Clin Oncol. 2001 Feb;24(1):43-6. link to original article contains dosing details in manuscript PubMed
  2. Fiorica JV, Brunetto VL, Hanjani P, Lentz SS, Mannel R, Andersen W; Gynecologic Oncology Group. Phase II trial of alternating courses of megestrol acetate and tamoxifen in advanced endometrial carcinoma: a Gynecologic Oncology Group study. Gynecol Oncol. 2004 Jan;92(1):10-4. link to original article contains dosing details in manuscript PubMed

Tamoxifen monotherapy

Regimen

Study Evidence
Quinn et al. 1989 Phase 2
Thigpen et al. 2001 (GOG-81F) Phase 2

Endocrine therapy

Continued indefinitely

References

  1. Quinn MA, Campbell JJ. Tamoxifen therapy in advanced/recurrent endometrial carcinoma. Gynecol Oncol. 1989 Jan;32(1):1-3. link to original article PubMed
  2. GOG-81F: Thigpen T, Brady MF, Homesley HD, Soper JT, Bell J. Tamoxifen in the treatment of advanced or recurrent endometrial carcinoma: a Gynecologic Oncology Group study. J Clin Oncol. 2001 Jan 15;19(2):364-7. link to original article contains dosing details in manuscript PubMed