Difference between revisions of "Endometrial cancer"

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'''Use of this site is subject to you reading and agreeing with the terms set forth in the [[HemOnc.org_-_A_Hematology_Oncology_Wiki:General_disclaimer|disclaimer]].'''
 
'''Use of this site is subject to you reading and agreeing with the terms set forth in the [[HemOnc.org_-_A_Hematology_Oncology_Wiki:General_disclaimer|disclaimer]].'''
  
Is there a regimen missing from this list? Would you like to share a different dosage/schedule or an additional reference for a regimen? Have you noticed an error? Do you have an idea that will help the site grow to better meet your needs and the needs of many others? You are [[How_to_contribute|invited to contribute to the site]].
+
Is there a regimen missing from this list? Would you like to share a different dosage/schedule or an additional reference for a regimen? Have you noticed an error? Do you have an idea that will help the site grow to better meet your needs and the needs of many others? You are [[How_to_contribute|invited to contribute to the site]].
  
 
{| class="wikitable" style="float:right; margin-right: 5px;"
 
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|<div style="background-color: #66FF66; border: 1px solid #808000; padding: 5px; {{border-radius|16px}}" align="right"><font size="4"><b>{{#ask: [[-Has subobject::{{FULLPAGENAME}}]] |?Regimen |limit=10000|format=sum}} regimens on this page</b></font></div>
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|<div style="background-color: #66FF66; border: 1px solid #808000; padding: 5px; {{border-radius|16px}}" align="right"><font size="4"><b>{{#ask: [[-Has subobject::{{FULLPAGENAME}}]] |?Regimen |limit=10000|format=sum}} regimens on this page</b></font></div>
<div style="background-color: #66CCFF; border: 1px solid #808000; padding: 5px; {{border-radius|16px}}"><font size="4"><b>{{#ask: [[-Has subobject::{{FULLPAGENAME}}]] |?Variant |limit=10000|format=sum}} variants on this page</b></font></div>
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<div style="background-color: #66CCFF; border: 1px solid #808000; padding: 5px; {{border-radius|16px}}"><font size="4"><b>{{#ask: [[-Has subobject::{{FULLPAGENAME}}]] |?Variant |limit=10000|format=sum}} variants on this page</b></font></div>
 
|}
 
|}
 
{{TOC limit|limit=3}}
 
{{TOC limit|limit=3}}
  
=Hormone therapy for endometrioid histologies=
+
=Endocrine therapy for endometrioid histologies=
 
==Anastrozole (Arimidex) {{#subobject:534a|Regimen=1}}==
 
==Anastrozole (Arimidex) {{#subobject:534a|Regimen=1}}==
 
{| class="wikitable" style="float:right; margin-left: 5px;"
 
{| class="wikitable" style="float:right; margin-left: 5px;"
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|[[#toc|back to top]]
 
|[[#toc|back to top]]
 
|}
 
|}
Level of Evidence:
+
===Regimen {{#subobject:8c4e67|Variant=1}}===
<span  
+
{| border="1" style="text-align:center;" !align="left"
 +
|'''Study'''
 +
|[[Levels_of_Evidence#Evidence|'''Evidence''']]
 +
|-
 +
|[http://www.gynecologiconcology-online.net/article/S0090-8258(00)95865-7/abstract Rose et al. 2000]
 +
|<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;
 
padding:3px 6px 3px 6px;
 
padding:3px 6px 3px 6px;
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border-width:2px;
 
border-width:2px;
 
border-style:solid;">Phase II</span>
 
border-style:solid;">Phase II</span>
 
+
|-
 +
|}
 +
====Endocrine therapy====
 
*[[Anastrozole (Arimidex)]] 1 mg PO once per day
 
*[[Anastrozole (Arimidex)]] 1 mg PO once per day
  
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===References===
 
===References===
# Rose PG, Brunetto VL, VanLe L, Bell J, Walker JL, Lee RB. 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.sciencedirect.com/science/article/pii/S0090825800958657 link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/10926805 PubMed]
+
# Rose PG, Brunetto VL, VanLe L, Bell J, Walker JL, Lee RB. 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/abstract link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/10926805 PubMed]
  
 
==Medroxyprogesterone acetate (MPA) {{#subobject:6c7bb9|Regimen=1}}==
 
==Medroxyprogesterone acetate (MPA) {{#subobject:6c7bb9|Regimen=1}}==
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|-
 
|-
 
|}
 
|}
 
+
====Endocrine therapy====
 
*[[Medroxyprogesterone acetate (MPA)]] 200 mg PO once per day
 
*[[Medroxyprogesterone acetate (MPA)]] 200 mg PO once per day
  
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|}
 
|}
 
===Regimen {{#subobject:334b8c|Variant=1}}===
 
===Regimen {{#subobject:334b8c|Variant=1}}===
Level of Evidence:
+
{| border="1" style="text-align:center;" !align="left"
<span  
+
|'''Study'''
 +
|[[Levels_of_Evidence#Evidence|'''Evidence''']]
 +
|-
 +
|[http://www.gynecologiconcology-online.net/article/S0090-8258(03)00651-6/abstract Whitney et al. 2004]
 +
|<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;
 
padding:3px 6px 3px 6px;
 
padding:3px 6px 3px 6px;
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border-width:2px;
 
border-width:2px;
 
border-style:solid;">Phase II</span>
 
border-style:solid;">Phase II</span>
 
+
|-
 +
|}
 +
====Endocrine therapy====
 
*[[Medroxyprogesterone acetate (MPA)]] 100 mg PO BID on even-numbered weeks (for example, week 2, 4, 6, etc.)
 
*[[Medroxyprogesterone acetate (MPA)]] 100 mg PO BID on even-numbered weeks (for example, week 2, 4, 6, etc.)
 
*[[Tamoxifen (Nolvadex)]] 20 mg PO BID
 
*[[Tamoxifen (Nolvadex)]] 20 mg PO BID
  
'''given until progression of disease or unacceptable toxicity'''
+
'''Given until progression of disease or unacceptable toxicity'''
  
 
===References===
 
===References===
# Whitney CW, Brunetto VL, Zaino RJ, Lentz SS, Sorosky J, Armstrong DK, Lee RB; Gynecologic Oncology Group study. 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.sciencedirect.com/science/article/pii/S0090825803006516 link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/14751130 PubMed]
+
# Whitney CW, Brunetto VL, Zaino RJ, Lentz SS, Sorosky J, Armstrong DK, Lee RB; Gynecologic Oncology Group study. 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/abstract link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/14751130 PubMed]
  
 
==Megestrol acetate (Megace) {{#subobject:4b50ea|Regimen=1}}==
 
==Megestrol acetate (Megace) {{#subobject:4b50ea|Regimen=1}}==
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|-
 
|-
 
|}
 
|}
 
+
====Endocrine therapy====
 
*[[Megestrol acetate (Megace)]] 80 mg PO BID
 
*[[Megestrol acetate (Megace)]] 80 mg PO BID
  
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|-
 
|-
 
|}
 
|}
 
+
====Endocrine therapy====
 
*[[Megestrol acetate (Megace)]] 80 mg PO BID x 3 weeks, alternating with tamoxifen
 
*[[Megestrol acetate (Megace)]] 80 mg PO BID x 3 weeks, alternating with tamoxifen
 
*[[Tamoxifen (Nolvadex)]] 20 mg PO BID x 3 weeks, alternating with megestrol
 
*[[Tamoxifen (Nolvadex)]] 20 mg PO BID x 3 weeks, alternating with megestrol
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|}
 
|}
 
===Regimen {{#subobject:af71e3|Variant=1}}===
 
===Regimen {{#subobject:af71e3|Variant=1}}===
Level of Evidence:
+
{| border="1" style="text-align:center;" !align="left"
<span  
+
|'''Study'''
 +
|[[Levels_of_Evidence#Evidence|'''Evidence''']]
 +
|-
 +
|[http://www.sciencedirect.com/science/article/pii/0090825889908391 Quinn et al. 1989]
 +
|<span
 +
style="background:#EEEE00;
 +
padding:3px 6px 3px 6px;
 +
border-color:black;
 +
border-width:2px;
 +
border-style:solid;">Phase II</span>
 +
|-
 +
|[http://jco.ascopubs.org/content/19/2/364.long Thigpen et al. 2001]
 +
|<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;
 
padding:3px 6px 3px 6px;
 
padding:3px 6px 3px 6px;
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border-width:2px;
 
border-width:2px;
 
border-style:solid;">Phase II</span>
 
border-style:solid;">Phase II</span>
 
+
|-
 +
|}
 +
====Endocrine therapy====
 
*[[Tamoxifen (Nolvadex)]] 20 mg PO BID
 
*[[Tamoxifen (Nolvadex)]] 20 mg PO BID
  
'''given until progression of disease or unacceptable toxicity'''
+
'''Given until progression of disease or unacceptable toxicity'''
  
 
===References===
 
===References===
# Quinn MA, Campbell JJ. Tamoxifen therapy in advanced/recurrent endometrial carcinoma. Gynecol Oncol. 1989 Jan;32(1):1-3. [http://www.ncbi.nlm.nih.gov/pubmed/2909443 PubMed]
+
# Quinn MA, Campbell JJ. Tamoxifen therapy in advanced/recurrent endometrial carcinoma. Gynecol Oncol. 1989 Jan;32(1):1-3. [http://www.sciencedirect.com/science/article/pii/0090825889908391 link to SD article] [http://www.ncbi.nlm.nih.gov/pubmed/2909443 PubMed]
 
# 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. [http://jco.ascopubs.org/content/19/2/364.long link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/11208827 PubMed]
 
# 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. [http://jco.ascopubs.org/content/19/2/364.long link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/11208827 PubMed]
  
 
=Adjuvant radiation & chemotherapy=
 
=Adjuvant radiation & chemotherapy=
==Cisplatin, Doxorubicin, RT {{#subobject:4d10f0|Regimen=1}}==
+
==RT -> Cisplatin & Doxorubicin {{#subobject:4d10f0|Regimen=1}}==
 
{| class="wikitable" style="float:right; margin-left: 5px;"
 
{| class="wikitable" style="float:right; margin-left: 5px;"
 
|-
 
|-
 
|[[#toc|back to top]]
 
|[[#toc|back to top]]
 
|}
 
|}
 
 
RT: '''<u>R</u>'''adiation '''<u>T</u>'''herapy
 
RT: '''<u>R</u>'''adiation '''<u>T</u>'''herapy
  
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|-
 
|-
 
|}
 
|}
 
+
''Note: for chemotherapy, body surface area capped at 2.0 m<sup>2</sup>. Radiation is to begin within 8 weeks after surgery.''
====Adjuvant radiation====
+
====Radiotherapy====
 
*Radiation therapy to the pelvis, 1.8 Gy x 28 fractions (total dose: 50.4 Gy)
 
*Radiation therapy to the pelvis, 1.8 Gy x 28 fractions (total dose: 50.4 Gy)
 
**Patients with positive para-aortic lymph nodes received 1.5 to 1.8 Gy x 24 to 29 fractions (total dose: 43.5 Gy)
 
**Patients with positive para-aortic lymph nodes received 1.5 to 1.8 Gy x 24 to 29 fractions (total dose: 43.5 Gy)
  
'''6-week course, begins within 8 weeks after surgery'''
+
'''6-week course, followed within 8 weeks by:'''
  
 
====Chemotherapy====
 
====Chemotherapy====
*[[Cisplatin (Platinol)]] 50 mg/m2 IV once on day 1, given second
+
*[[Cisplatin (Platinol)]] 50 mg/m<sup>2</sup> IV once on day 1, '''given second'''
*[[Doxorubicin (Adriamycin)]] 45 mg/m2 IV once on day 1, given first
+
*[[Doxorubicin (Adriamycin)]] 45 mg/m<sup>2</sup> IV once on day 1, '''given first'''
*Body surface area capped at 2.0 m2
 
  
Supportive medications:
+
====Supportive medications====
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once daily on days 2-11, or until ANC increases to 10,000; or [[Pegfilgrastim (Neulasta)]]
+
*G-CSF, either of the following:
 +
**[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day on days 2 to 11, or until ANC increases to 10,000
 +
**[[Pegfilgrastim (Neulasta)]] 6 mg SC once on day 2
 
*[[Dexamethasone (Decadron)]] 10 mg IV once prior to chemotherapy
 
*[[Dexamethasone (Decadron)]] 10 mg IV once prior to chemotherapy
 
*[[antiemesis|5-HT3 antagonist]]
 
*[[antiemesis|5-HT3 antagonist]]
  
'''21-day cycle x 6 cycles, to start within 8 weeks after adjuvant radiation is complete'''
+
'''21-day cycle for 6 cycles'''
  
 
===References===
 
===References===
 
# 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/abstract link to original article] [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4459781/ link to PMC article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/19108877 PubMed]
 
# 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/abstract link to original article] [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4459781/ link to PMC article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/19108877 PubMed]
  
==Cisplatin, Doxorubicin, Paclitaxel, RT {{#subobject:24a846|Regimen=1}}==
+
==RT -> Cisplatin, Doxorubicin, Paclitaxel {{#subobject:24a846|Regimen=1}}==
 
{| class="wikitable" style="float:right; margin-left: 5px;"
 
{| class="wikitable" style="float:right; margin-left: 5px;"
 
|-
 
|-
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|-
 
|-
 
|}
 
|}
 
+
''Note: for chemotherapy, body surface area capped at 2.0 m<sup>2</sup>. Radiation is to start within 8 weeks after surgery.''
====Adjuvant radiation====
+
====Radiotherapy====
 
*Radiation therapy to the pelvis, 1.8 Gy x 28 fractions (total dose: 50.4 Gy)
 
*Radiation therapy to the pelvis, 1.8 Gy x 28 fractions (total dose: 50.4 Gy)
 
**Patients with positive para-aortic lymph nodes received 1.5 to 1.8 Gy x 24 to 29 fractions (total dose: 43.5 Gy)
 
**Patients with positive para-aortic lymph nodes received 1.5 to 1.8 Gy x 24 to 29 fractions (total dose: 43.5 Gy)
  
'''6-week course, begins within 8 weeks after surgery'''
+
'''6-week course, followed within 8 weeks by:'''
  
 
====Chemotherapy====
 
====Chemotherapy====
*[[Cisplatin (Platinol)]] 50 mg/m2 IV once on day 1, given second
+
*[[Cisplatin (Platinol)]] 50 mg/m<sup>2</sup> IV once on day 1, '''given second'''
*[[Doxorubicin (Adriamycin)]] 45 mg/m2 IV once on day 1, given first
+
*[[Doxorubicin (Adriamycin)]] 45 mg/m<sup>2</sup> IV once on day 1, '''given first'''
*[[Paclitaxel (Taxol)]] 160 mg/m2 IV over 3 hours once on day 2
+
*[[Paclitaxel (Taxol)]] 160 mg/m<sup>2</sup> IV over 3 hours once on day 2
*Body surface area capped at 2.0 m2
 
  
Supportive medications:
+
====Supportive medications====
 
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day on days 3 to 12, or until ANC increases to 10,000
 
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day on days 3 to 12, or until ANC increases to 10,000
 
*[[Dexamethasone (Decadron)]] 10 mg IV once prior to day 1 chemotherapy; [[Dexamethasone (Decadron)]] 20 mg once 5 to 12 hours prior to paclitaxel on day 2
 
*[[Dexamethasone (Decadron)]] 10 mg IV once prior to day 1 chemotherapy; [[Dexamethasone (Decadron)]] 20 mg once 5 to 12 hours prior to paclitaxel on day 2
 
*[[antiemesis|5-HT3 antagonist]]
 
*[[antiemesis|5-HT3 antagonist]]
  
'''21-day cycle x 6 cycles, to start within 8 weeks after adjuvant radiation is complete'''
+
'''21-day cycle for 6 cycles'''
  
 
===References===
 
===References===
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|[[#toc|back to top]]
 
|[[#toc|back to top]]
 
|}
 
|}
===Regimen, Aghajanian et al. 2011 {{#subobject:8159f4|Variant=1}}===
+
===Regimen {{#subobject:8159f4|Variant=1}}===
Level of Evidence:
+
{| border="1" style="text-align:center;" !align="left"
<span  
+
|'''Study'''
 +
|[[Levels_of_Evidence#Evidence|'''Evidence''']]
 +
|-
 +
|[http://jco.ascopubs.org/content/29/16/2259.long Aghajanian et al. 2011]
 +
|<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;
 
padding:3px 6px 3px 6px;
 
padding:3px 6px 3px 6px;
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border-width:2px;
 
border-width:2px;
 
border-style:solid;">Phase II</span>
 
border-style:solid;">Phase II</span>
 
+
|-
 +
|}
 +
====Chemotherapy====
 
*[[Bevacizumab (Avastin)]] 15 mg/kg IV once on day 1
 
*[[Bevacizumab (Avastin)]] 15 mg/kg IV once on day 1
  
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===References===
 
===References===
# Aghajanian C, Sill MW, Darcy KM, Greer B, McMeekin DS, Rose PG, Rotmensch J, Barnes MN, Hanjani P, Leslie KK. 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. doi: 10.1200/JCO.2010.32.6397. Epub 2011 May 2. [http://jco.ascopubs.org/content/29/16/2259.long link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/21537039 PubMed]
+
<!-- Presented in part at the 45th Annual Meeting of the American Society of Clinical Oncology, May 29-June 2, 2009, Orlando, FL. -->
 +
# Aghajanian C, Sill MW, Darcy KM, Greer B, McMeekin DS, Rose PG, Rotmensch J, Barnes MN, Hanjani P, Leslie KK. 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. [http://jco.ascopubs.org/content/29/16/2259.long link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/21537039 PubMed]
  
 
==Carboplatin (Paraplatin) {{#subobject:f9b8ad|Regimen=1}}==
 
==Carboplatin (Paraplatin) {{#subobject:f9b8ad|Regimen=1}}==
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|}
 
|}
 
===Regimen {{#subobject:6a2df1|Variant=1}}===
 
===Regimen {{#subobject:6a2df1|Variant=1}}===
Level of Evidence:
+
{| border="1" style="text-align:center;" !align="left"
<span  
+
|'''Study'''
 +
|[[Levels_of_Evidence#Evidence|'''Evidence''']]
 +
|-
 +
|[http://www.ejcancer.info/article/S0959-8049%2802%2900504-X/abstract van Wijk et al. 2003]
 +
|<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;
 
padding:3px 6px 3px 6px;
 
padding:3px 6px 3px 6px;
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border-width:2px;
 
border-width:2px;
 
border-style:solid;">Phase II</span>
 
border-style:solid;">Phase II</span>
 
+
|-
*[[Carboplatin (Paraplatin)]] 400 mg/m2 IV over 30 minutes once on day 1
+
|}
**Dosage for patients with previously treated with chemotherapy is [[Carboplatin (Paraplatin)]] 300 mg/m2 IV over 30 minutes once on day 1
+
====Chemotherapy====
 +
*[[Carboplatin (Paraplatin)]] 400 mg/m<sup>2</sup> IV over 30 minutes once on day 1
 +
**Dosage for patients with previously treated with chemotherapy is [[Carboplatin (Paraplatin)]] 300 mg/m<sup>2</sup> IV over 30 minutes once on day 1
  
 
'''28-day cycles'''
 
'''28-day cycles'''
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|[[#toc|back to top]]
 
|[[#toc|back to top]]
 
|}
 
|}
===Regimen, Pignata et al. 2007 (END-1) {{#subobject:d48f39|Variant=1}}===
+
===Regimen {{#subobject:d48f39|Variant=1}}===
Level of Evidence:
+
{| border="1" style="text-align:center;" !align="left"
<span  
+
|'''Study'''
 +
|[[Levels_of_Evidence#Evidence|'''Evidence''']]
 +
|-
 +
|[http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2359926/ Pignata et al. 2007 (END-1)]
 +
|<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;
 
padding:3px 6px 3px 6px;
 
padding:3px 6px 3px 6px;
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border-width:2px;
 
border-width:2px;
 
border-style:solid;">Phase II</span>
 
border-style:solid;">Phase II</span>
 +
|-
 +
|}
 +
====Chemotherapy====
 +
*[[Carboplatin (Paraplatin)]] AUC 5 IV over 30 minutes once on day 1, '''given first'''
 +
*[[Doxorubicin liposomal (Doxil)]] 40 mg/m<sup>2</sup> IV over 60 minutes once on day 1, '''given second'''
  
*[[Carboplatin (Paraplatin)]] AUC 5 IV over 30 minutes once on day 1, given first
+
====Supportive medications====
*[[Doxorubicin liposomal (Doxil)]] 40 mg/m2 IV over 60 minutes once on day 1, given second
+
*"No prophylactic use of [[Filgrastim (Neupogen)|G-CSF]] was recommended. In case of grade 4 neutropaenia, even without fever, therapeutic and prophylactic use of G-CSF was allowed."
  
'''28-day cycles x 3 to 6 cycles;''' all patients received 3 cycles of therapy.  If there was no unacceptable toxicity, patients with stable or responsive disease received an additional 3 cycles.
+
'''28-day cycle for 3 to 6 cycles'''  
  
Supportive medications:
+
''All patients received 3 cycles of therapy. If there was no unacceptable toxicity, patients with stable or responsive disease received an additional 3 cycles.''
*"No prophylactic use of [[Filgrastim (Neupogen)|G-CSF]] was recommended. In case of grade 4 neutropaenia, even without fever, therapeutic and prophylactic use of G-CSF was allowed."
 
  
 
===References===
 
===References===
# 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. [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2359926/ link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/17486128 PubMed]
+
# 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. [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2359926/ link to PMC article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/17486128 PubMed]
  
 
==Carboplatin & Paclitaxel {{#subobject:b0e21f|Regimen=1}}==
 
==Carboplatin & Paclitaxel {{#subobject:b0e21f|Regimen=1}}==
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|[[#toc|back to top]]
 
|[[#toc|back to top]]
 
|}
 
|}
===Regimen #1, Pectasides et al. 2008 {{#subobject:7ab5c0|Variant=1}}===
+
===Regimen #1 {{#subobject:7ab5c0|Variant=1}}===
Level of Evidence:
+
{| border="1" style="text-align:center;" !align="left"
<span  
+
|'''Study'''
 +
|[[Levels_of_Evidence#Evidence|'''Evidence''']]
 +
|-
 +
|[http://www.gynecologiconcology-online.net/article/S0090-8258(08)00083-8/abstract Pectasides et al. 2008]
 +
|<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;
 
padding:3px 6px 3px 6px;
 
padding:3px 6px 3px 6px;
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border-width:2px;
 
border-width:2px;
 
border-style:solid;">Phase II</span>
 
border-style:solid;">Phase II</span>
 +
|-
 +
|}
 +
====Chemotherapy====
 +
*[[Carboplatin (Paraplatin)]] AUC 5 IV over 1 hour once on day 1, '''given second'''
 +
*[[Paclitaxel (Taxol)]] 175 mg/m<sup>2</sup> IV over 3 hours once on day 1, '''given first'''
  
*[[Carboplatin (Paraplatin)]] AUC 5 IV over 1 hour once on day 1, given second
+
'''21-day cycle for 6 to 9 cycles'''
*[[Paclitaxel (Taxol)]] 175 mg/m2 IV over 3 hours once on day 1, given first
 
  
'''21-day cycles x 6 to 9 cycles'''
+
===Regimen #2 {{#subobject:3a58ce|Variant=1}}===
 
+
{| border="1" style="text-align:center;" !align="left"
===Regimen #2, Hoskins et al. 2001 & Shechter-Maor et al. 2008 {{#subobject:3a58ce|Variant=1}}===
+
|'''Study'''
Level of Evidence:
+
|[[Levels_of_Evidence#Evidence|'''Evidence''']]
<span  
+
|-
 +
|[http://jco.ascopubs.org/content/19/20/4048.long Hoskins et al. 2001]
 +
|<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;
 
padding:3px 6px 3px 6px;
 
padding:3px 6px 3px 6px;
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border-width:2px;
 
border-width:2px;
 
border-style:solid;">Phase II</span>
 
border-style:solid;">Phase II</span>
 
+
|-
*[[Carboplatin (Paraplatin)]] AUC 5 to 7 IV once on day 1, given second
+
|}
*[[Paclitaxel (Taxol)]] 175 mg/m2 IV over 3 hours once on day 1, given first
+
====Chemotherapy====
 +
*[[Carboplatin (Paraplatin)]] AUC 5 to 7 IV 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'''
 
'''21-day cycles'''
  
===Regimen #3, Sorbe et al. 2008 {{#subobject:100919|Variant=1}}===
+
===Regimen #3 {{#subobject:100919|Variant=1}}===
Level of Evidence:
+
{| border="1" style="text-align:center;" !align="left"
<span  
+
|'''Study'''
 +
|[[Levels_of_Evidence#Evidence|'''Evidence''']]
 +
|-
 +
|[http://journals.lww.com/ijgc/Fulltext/2008/07000/Treatment_of_primary_advanced_and_recurrent.30.aspx Sorbe et al. 2008]
 +
|<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;
 
padding:3px 6px 3px 6px;
 
padding:3px 6px 3px 6px;
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border-width:2px;
 
border-width:2px;
 
border-style:solid;">Phase II</span>
 
border-style:solid;">Phase II</span>
 
+
|-
*[[Carboplatin (Paraplatin)]] AUC 5 IV once on day 1
+
|}
*[[Paclitaxel (Taxol)]] 175 mg/m2 IV once on day 1
+
====Chemotherapy====
 +
*[[Carboplatin (Paraplatin)]] AUC 5 IV over 1 hour once on day 1
 +
*[[Paclitaxel (Taxol)]] 175 mg/m<sup>2</sup> IV over 3 hours once on day 1
  
 
'''21-day cycles'''
 
'''21-day cycles'''
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===References===
 
===References===
 
# 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. [http://jco.ascopubs.org/content/19/20/4048.long link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/11600606 PubMed]
 
# 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. [http://jco.ascopubs.org/content/19/20/4048.long link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/11600606 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.sciencedirect.com/science/article/pii/S0090825808000838 link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/18299146 PubMed] content property of [http://hemonc.org HemOnc.org]
+
# 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/abstract link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/18299146 PubMed] content property of [http://hemonc.org HemOnc.org]
# 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. [http://www.ncbi.nlm.nih.gov/pubmed/17944917 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. [http://journals.lww.com/ijgc/Fulltext/2008/07000/Treatment_of_primary_advanced_and_recurrent.30.aspx link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/17944917 PubMed]
 
# '''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. [http://journals.lww.com/ijgc/pages/articleviewer.aspx?year=2009&issue=05000&article=00029&type=abstract link to original article] [http://www.ncbi.nlm.nih.gov/pubmed/19509567 PubMed]
 
# '''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. [http://journals.lww.com/ijgc/pages/articleviewer.aspx?year=2009&issue=05000&article=00029&type=abstract link to original article] [http://www.ncbi.nlm.nih.gov/pubmed/19509567 PubMed]
  
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|-
 
|-
 
|}
 
|}
 +
''Note: body surface area capped at 2.0 m<sup>2</sup>.''
 +
====Chemotherapy====
 +
*[[Cisplatin (Platinol)]] 50 mg/m<sup>2</sup> IV over 1 hour once on day 1, '''given second'''
 +
*[[Doxorubicin (Adriamycin)]] 60 mg/m<sup>2</sup> IV once on day 1, '''given first'''
 +
**Dosage for patients with previous pelvic radiation or who were >65 years old is [[Doxorubicin (Adriamycin)]] 45 mg/m<sup>2</sup> IV once on day 1
  
*[[Cisplatin (Platinol)]] 50 mg/m2 IV over 1 hour once on day 1, '''given second'''
+
'''21-day cycle for 7 cycles'''
*[[Doxorubicin (Adriamycin)]] 60 mg/m2 IV once on day 1, '''given first'''
 
**Dosage for patients with previous pelvic radiation or who were >65 years old is [[Doxorubicin (Adriamycin)]] 45 mg/m2 IV once on day 1
 
*Body surface area capped at 2.0 m2
 
 
 
'''21-day cycle x 7 cycles'''
 
  
 
===Regimen #2 {{#subobject:5baa3b|Variant=1}}===
 
===Regimen #2 {{#subobject:5baa3b|Variant=1}}===
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|-
 
|-
 
|}
 
|}
 
+
====Chemotherapy====
*[[Cisplatin (Platinol)]] 50 mg/m2 IV once on day 1 of cycles 1 to 8
+
*[[Cisplatin (Platinol)]] 50 mg/m<sup>2</sup> IV once on day 1 of cycles 1 to 8
*[[Doxorubicin (Adriamycin)]] 60 mg/m2 IV once on day 1 of cycles 1 to 7
+
*[[Doxorubicin (Adriamycin)]] 60 mg/m<sup>2</sup> IV once on day 1 of cycles 1 to 7
  
 
Supportive hydration:
 
Supportive hydration:
 
*Normal saline at 500 mL/H for 2 hours prior to and after cisplatin
 
*Normal saline at 500 mL/H for 2 hours prior to and after cisplatin
  
'''21-day cycle x 8 cycles'''
+
'''21-day cycle for 8 cycles'''
  
 
===References===
 
===References===
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|-
 
|-
 
|}
 
|}
 +
''Note: body surface area capped at 2.0 m<sup>2</sup>.''
 +
====Chemotherapy====
 +
*[[Cisplatin (Platinol)]] 50 mg/m<sup>2</sup> IV over 1 hour once on day 1, '''given second'''
 +
*[[Doxorubicin (Adriamycin)]] 45 mg/m<sup>2</sup> IV once on day 1, '''given first'''
 +
*[[Paclitaxel (Taxol)]] 160 mg/m<sup>2</sup> IV over 3 hours once on day 2
  
*[[Cisplatin (Platinol)]] 50 mg/m2 IV over 1 hour once on day 1, '''given second'''
+
====Supportive medications====
*[[Doxorubicin (Adriamycin)]] 45 mg/m2 IV once on day 1, '''given first'''
 
*[[Paclitaxel (Taxol)]] 160 mg/m2 IV over 3 hours once on day 2
 
*Body surface area capped at 2.0 m2
 
 
 
Supportive medications:
 
 
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day on days 3 to 12
 
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day on days 3 to 12
  
'''21-day cycle x 7 cycles'''
+
'''21-day cycle for 7 cycles'''
  
 
===References===
 
===References===
Line 495: Line 560:
 
|-
 
|-
 
|}
 
|}
 +
====Chemotherapy====
 +
*[[Cisplatin (Platinol)]] 20 mg/m<sup>2</sup> IV at an infusion rate of approximately 1 mg/min once per day on days 1 to 4, '''given first'''
 +
*[[Ifosfamide (Ifex)]] 1500 mg/m<sup>2</sup> IV over 1 hour once per day on days 1 to 4, '''given second together with [[Mesna (Mesnex)]]'''
  
*[[Cisplatin (Platinol)]] 20 mg/m2 IV at an infusion rate of approximately 1 mg/min once per day on days 1 to 4, '''given first'''
+
====Supportive medications====
*[[Ifosfamide (Ifex)]] 1500 mg/m2 IV over 1 hour once per day on days 1 to 4, '''given second together with mesna'''
+
*[[Mesna (Mesnex)]] 120 mg/m<sup>2</sup> IV bolus over 15 minutes once on day 1, then 1500 mg/m<sup>2</sup>/day IV continuous infusion over 96 hours on days 1 to 4, '''given second together with [[Ifosfamide (Ifex)]]'''
*[[Mesna (Mesnex)]] 120 mg/m2 IV bolus over 15 minutes once on day 1, then 1500 mg/m2/day IV continuous infusion over 96 hours on days 1 to 4, '''given second together with ifosfamide'''
 
 
 
Supportive medications:
 
 
*Suggested hydration: 1 liter of NS or 1/2 NS given over several hours prior to chemotherapy
 
*Suggested hydration: 1 liter of NS or 1/2 NS given over several hours prior to chemotherapy
  
'''21-day cycle x 3 cycles'''
+
'''21-day cycle for 3 cycles'''
  
 
===References===
 
===References===
Line 514: Line 579:
 
|}
 
|}
 
===Regimen {{#subobject:b3c8fd|Variant=1}}===
 
===Regimen {{#subobject:b3c8fd|Variant=1}}===
Level of Evidence:
+
{| border="1" style="text-align:center;" !align="left"
<span  
+
|'''Study'''
 +
|[[Levels_of_Evidence#Evidence|'''Evidence''']]
 +
|-
 +
|[http://www.gynecologiconcology-online.net/article/S0090-8258(00)95827-X/abstract Dimopoulos et al. 2000]
 +
|<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;
 
padding:3px 6px 3px 6px;
 
padding:3px 6px 3px 6px;
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border-width:2px;
 
border-width:2px;
 
border-style:solid;">Phase II</span>
 
border-style:solid;">Phase II</span>
 +
|-
 +
|}
 +
====Chemotherapy====
 +
*[[Cisplatin (Platinol)]] 75 mg/m<sup>2</sup> IV over 2 hours once on day 1, '''given second'''
 +
*[[Paclitaxel (Taxol)]] 175 mg/m<sup>2</sup> IV over 3 hours once on day 1, '''given first'''
  
*[[Cisplatin (Platinol)]] 75 mg/m2 IV over 2 hours once on day 1, given second
+
====Supportive medications====
*[[Paclitaxel (Taxol)]] 175 mg/m2 IV over 3 hours once on day 1, given first
+
*[[Dexamethasone (Decadron)]] 20 mg PO/IV given twice, 12 and 6 hours prior to [[Paclitaxel (Taxol)]]
 
+
*Diphenhydramine (Benadryl) 25 mg IV once 30 minutes prior to [[Paclitaxel (Taxol)]]
'''21-day cycles x up to 6 cycles'''
+
*Ranitidine (Zantac) 50 mg IV once 30 minutes prior to [[Paclitaxel (Taxol)]]
 
+
*900 mL normal saline mixed with 100 mL mannitol given over 1 hour prior to [[Cisplatin (Platinol)]]
Supportive medications:
+
*2 liters NS with potassium & magnesium after [[Cisplatin (Platinol)]]
*[[Dexamethasone (Decadron)]] 20 mg PO/IV given twice, 12 and 6 hours prior to paclitaxel
 
*Diphenhydramine (Benadryl) 25 mg IV once 30 minutes prior to paclitaxel
 
*Ranitidine (Zantac) 50 mg IV once 30 minutes prior to paclitaxel
 
*900 mL normal saline mixed with 100 mL mannitol given over 1 hour prior to cisplatin
 
*2 liters NS with potassium & magnesium after cisplatin
 
 
*"Appropriate [[antiemesis|antiemetics]]"
 
*"Appropriate [[antiemesis|antiemetics]]"
 
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day, starting on day 5 and continuing until WBC >10,000
 
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day, starting on day 5 and continuing until WBC >10,000
 +
 +
'''21-day cycle for up to 6 cycles'''
  
 
===References===
 
===References===
# 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.sciencedirect.com/science/article/pii/S009082580095827X link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/10873410 PubMed]
+
# 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/abstract link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/10873410 PubMed]
  
 
==Dactinomycin (Cosmegen) {{#subobject:97a01a|Regimen=1}}==
 
==Dactinomycin (Cosmegen) {{#subobject:97a01a|Regimen=1}}==
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|}
 
|}
 
===Regimen {{#subobject:2019ab|Variant=1}}===
 
===Regimen {{#subobject:2019ab|Variant=1}}===
Level of Evidence:
+
{| border="1" style="text-align:center;" !align="left"
<span  
+
|'''Study'''
 +
|[[Levels_of_Evidence#Evidence|'''Evidence''']]
 +
|-
 +
|[http://www.gynecologiconcology-online.net/article/S0090-8258(99)95652-4/abstract Moore et al. 1999]
 +
|<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;
 
padding:3px 6px 3px 6px;
 
padding:3px 6px 3px 6px;
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border-width:2px;
 
border-width:2px;
 
border-style:solid;">Phase II</span>
 
border-style:solid;">Phase II</span>
 
+
|-
*[[Dactinomycin (Cosmegen)]] 2 mg/m2 IV over 15 minutes once on day 1
+
|}
 +
====Chemotherapy====
 +
*[[Dactinomycin (Cosmegen)]] 2 mg/m<sup>2</sup> IV over 15 minutes once on day 1
  
 
'''28-day cycles'''
 
'''28-day cycles'''
  
 
===References===
 
===References===
# Moore DH, Blessing JA, Dunton C, Buller RE, Reid GC. 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.sciencedirect.com/science/article/pii/S0090825899956524 link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/10600310 PubMed]
+
# Moore DH, Blessing JA, Dunton C, Buller RE, Reid GC. 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/abstract link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/10600310 PubMed]
  
 
==Ifosfamide {{#subobject:b078a0|Regimen=1}}==
 
==Ifosfamide {{#subobject:b078a0|Regimen=1}}==
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|}
 
|}
  
''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.''
+
''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.''
*[[Ifosfamide (Ifex)]] 1600 mg/m2 IV once per day on days 1 to 3
+
====Chemotherapy====
**Dosage for patients with previous radiation is [[Ifosfamide (Ifex)]] 1200 mg/m2 IV once per day on days 1 to 3  
+
*[[Ifosfamide (Ifex)]] 1600 mg/m<sup>2</sup> IV once per day on days 1 to 3
 +
**Dosage for patients with previous radiation is [[Ifosfamide (Ifex)]] 1200 mg/m<sup>2</sup> IV once per day on days 1 to 3  
  
Supportive medications:
+
====Supportive medications====
 
*[[Mesna (Mesnex)]] 2000 mg IV over 12 hours once per day on days 1 to 3, starting 15 minutes before [[Ifosfamide (Ifex)]]
 
*[[Mesna (Mesnex)]] 2000 mg IV over 12 hours once per day on days 1 to 3, starting 15 minutes before [[Ifosfamide (Ifex)]]
 
**Alternate PO dosing: [[Mesna (Mesnex)]] 1330 mg PO taken three times per day, 1 hour before, 4 hours after, and 8 hours after [[Ifosfamide (Ifex)]] (4000 mg total dose per day), on days 1 to 3
 
**Alternate PO dosing: [[Mesna (Mesnex)]] 1330 mg PO taken three times per day, 1 hour before, 4 hours after, and 8 hours after [[Ifosfamide (Ifex)]] (4000 mg total dose per day), on days 1 to 3
 
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day starting on day 4, to continue until ANC is greater than or equal to 2000
 
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day starting on day 4, to continue until ANC is greater than or equal to 2000
  
'''21-day cycle x 8 cycles'''
+
'''21-day cycle for 8 cycles'''
  
 
===References===
 
===References===
Line 618: Line 696:
 
|}
 
|}
  
''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.''
+
''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.''
*[[Ifosfamide (Ifex)]] 1600 mg/m2 IV once per day on days 1 to 3
+
====Chemotherapy====
**Dosage for patients with previous radiation is [[Ifosfamide (Ifex)]] 1200 mg/m2 IV once per day on days 1 to 3  
+
*[[Ifosfamide (Ifex)]] 1600 mg/m<sup>2</sup> IV once per day on days 1 to 3
*[[Paclitaxel (Taxol)]] 135 mg/m2 IV over 3 hours once on day 1
+
**Dosage for patients with previous radiation is [[Ifosfamide (Ifex)]] 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 medications:
+
====Supportive medications====
 
*[[Mesna (Mesnex)]] 2000 mg IV over 12 hours once per day on days 1 to 3, starting 15 minutes before [[Ifosfamide (Ifex)]]
 
*[[Mesna (Mesnex)]] 2000 mg IV over 12 hours once per day on days 1 to 3, starting 15 minutes before [[Ifosfamide (Ifex)]]
 
**Alternate PO dosing: [[Mesna (Mesnex)]] 1330 mg PO taken three times per day, 1 hour before, 4 hours after, and 8 hours after [[Ifosfamide (Ifex)]] (4000 mg total dose per day), on days 1 to 3
 
**Alternate PO dosing: [[Mesna (Mesnex)]] 1330 mg PO taken three times per day, 1 hour before, 4 hours after, and 8 hours after [[Ifosfamide (Ifex)]] (4000 mg total dose per day), on days 1 to 3
Line 631: Line 710:
 
*[[Cimetidine (Tagamet)]] 300 mg IV or [[Ranitidine (Zantac)]] 50 mg IV once 30 minutes prior to [[Paclitaxel (Taxol)]]
 
*[[Cimetidine (Tagamet)]] 300 mg IV or [[Ranitidine (Zantac)]] 50 mg IV once 30 minutes prior to [[Paclitaxel (Taxol)]]
  
'''21-day cycle x 8 cycles'''
+
'''21-day cycle for 8 cycles'''
  
 
===References===
 
===References===
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|[[#toc|back to top]]
 
|[[#toc|back to top]]
 
|}
 
|}
===Regimen #1, Lincoln et al. 2003 {{#subobject:a2c4fa|Variant=1}}===
+
===Regimen #1 {{#subobject:a2c4fa|Variant=1}}===
Level of Evidence:
+
{| border="1" style="text-align:center;" !align="left"
<span  
+
|'''Study'''
 +
|[[Levels_of_Evidence#Evidence|'''Evidence''']]
 +
|-
 +
|[http://www.gynecologiconcology-online.net/article/S0090-8258(02)00068-9/abstract Lincoln et al. 2003]
 +
|<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;
 
padding:3px 6px 3px 6px;
 
padding:3px 6px 3px 6px;
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border-width:2px;
 
border-width:2px;
 
border-style:solid;">Phase II</span>
 
border-style:solid;">Phase II</span>
 +
|-
 +
|}
 +
====Chemotherapy====
 +
*[[Paclitaxel (Taxol)]] 200 mg/m<sup>2</sup> IV over 3 hours once on day 1
 +
**Dosage for patients with previous pelvic radiation is [[Paclitaxel (Taxol)]] 175 mg/m<sup>2</sup> IV over 3 hours once on day 1
 +
**Dose of [[Paclitaxel (Taxol)]] can be changed to 135 or 110 mg/m<sup>2</sup> depending on toxicity
  
*[[Paclitaxel (Taxol)]] 200 mg/m2 IV over 3 hours once on day 1
+
====Supportive medications====
**Dosage for patients with previous pelvic radiation is [[Paclitaxel (Taxol)]] 175 mg/m2 IV over 3 hours once on day 1
 
**Dose of [[Paclitaxel (Taxol)]] can be changed to 135 or 110 mg/m2 depending on toxicity
 
 
 
'''21-day cycles'''
 
 
 
Supportive medications:
 
 
*[[Dexamethasone (Decadron)]] 20 mg PO/IV given twice, 12 and 6 hours prior to paclitaxel
 
*[[Dexamethasone (Decadron)]] 20 mg PO/IV given twice, 12 and 6 hours prior to paclitaxel
 
*Diphenhydramine (Benadryl) 50 mg PO/IV once 30 minutes prior to paclitaxel
 
*Diphenhydramine (Benadryl) 50 mg PO/IV once 30 minutes prior to paclitaxel
 
*Cimetidine (Tagamet) 300 mg IV once 30 minutes prior to paclitaxel
 
*Cimetidine (Tagamet) 300 mg IV once 30 minutes prior to paclitaxel
  
===Regimen #2, Lissoni et al. 1996 {{#subobject:f1656b|Variant=1}}===
+
'''21-day cycles'''
Level of Evidence:
+
 
<span  
+
===Regimen #2 {{#subobject:f1656b|Variant=1}}===
 +
{| border="1" style="text-align:center;" !align="left"
 +
|'''Study'''
 +
|[[Levels_of_Evidence#Evidence|'''Evidence''']]
 +
|-
 +
|[http://annonc.oxfordjournals.org/content/7/8/861.long Lissoni et al. 1996]
 +
|<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;
 
padding:3px 6px 3px 6px;
 
padding:3px 6px 3px 6px;
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border-width:2px;
 
border-width:2px;
 
border-style:solid;">Phase II</span>
 
border-style:solid;">Phase II</span>
 +
|-
 +
|}
 +
====Chemotherapy====
 +
*[[Paclitaxel (Taxol)]] 175 mg/m<sup>2</sup> IV over 3 hours once on day 1
  
*[[Paclitaxel (Taxol)]] 175 mg/m2 IV over 3 hours once on day 1
+
====Supportive medications====
 
 
'''21-day cycles'''
 
 
 
Supportive medications:
 
 
*Hydrocortisone (Cortef) 250 mg IV once 1 hour prior to paclitaxel
 
*Hydrocortisone (Cortef) 250 mg IV once 1 hour prior to paclitaxel
 
*Chlorphenamine/chlorpheniramine (H1 blocker) 10 mg IM once 1 hour prior to paclitaxel
 
*Chlorphenamine/chlorpheniramine (H1 blocker) 10 mg IM once 1 hour prior to paclitaxel
 
*Cimetidine (Tagamet) 300 mg IV once 1 hour prior to paclitaxel
 
*Cimetidine (Tagamet) 300 mg IV once 1 hour prior to paclitaxel
  
===Regimen #3, Ball et al. 1996 {{#subobject:68d2e|Variant=1}}===
+
'''21-day cycles'''
Level of Evidence:
+
 
<span  
+
===Regimen #3 {{#subobject:68d2e|Variant=1}}===
 +
{| border="1" style="text-align:center;" !align="left"
 +
|'''Study'''
 +
|[[Levels_of_Evidence#Evidence|'''Evidence''']]
 +
|-
 +
|[http://www.gynecologiconcology-online.net/article/S0090-8258(96)90227-9/abstract Ball et al. 1996]
 +
|<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;
 
padding:3px 6px 3px 6px;
 
padding:3px 6px 3px 6px;
Line 687: Line 782:
 
border-width:2px;
 
border-width:2px;
 
border-style:solid;">Phase II</span>
 
border-style:solid;">Phase II</span>
 +
|-
 +
|}
 +
====Chemotherapy====
 +
*[[Paclitaxel (Taxol)]] 250 mg/m<sup>2</sup> IV continuous infusion over 24 hours once on day 1
 +
**Dosage for patients with previous pelvic radiation is 200 mg/m<sup>2</sup> IV continuous infusion over 24 hours once on day 1
 +
**Dose can be changed to 200, 170, 135, 110 mg/m<sup>2</sup> depending on toxicity
  
*[[Paclitaxel (Taxol)]] 250 mg/m2 IV continuous infusion over 24 hours once on day 1
+
====Supportive medications====
**Dosage for patients with previous pelvic radiation is [[Paclitaxel (Taxol)]] 200 mg/m2 IV continuous infusion over 24 hours once on day 1
 
**Dose of [[Paclitaxel (Taxol)]] can be changed to 200, 170, 135, 110 mg/m2 depending on toxicity
 
 
 
'''21-day cycles'''
 
 
 
Supportive medications:
 
 
*[[Dexamethasone (Decadron)]] 20 mg PO/IV given twice, 12 and 6 hours prior to paclitaxel
 
*[[Dexamethasone (Decadron)]] 20 mg PO/IV given twice, 12 and 6 hours prior to paclitaxel
 
*Diphenhydramine (Benadryl) 50 mg PO/IV once 30 minutes prior to paclitaxel
 
*Diphenhydramine (Benadryl) 50 mg PO/IV once 30 minutes prior to paclitaxel
 
*Cimetidine (Tagamet) 300 mg IV once 30 minutes prior to paclitaxel
 
*Cimetidine (Tagamet) 300 mg IV once 30 minutes prior to paclitaxel
 
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day starting on day 3, 24 hours after chemotherapy, continued for at least 12 days or until two successive total leukocyte counts are 10,000 or greater, whichever comes last
 
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day starting on day 3, 24 hours after chemotherapy, continued for at least 12 days or until two successive total leukocyte counts are 10,000 or greater, whichever comes last
 +
 +
'''21-day cycles'''
  
 
===References===
 
===References===
# Ball HG, Blessing JA, Lentz SS, Mutch DG. 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.sciencedirect.com/science/article/pii/S0090825896902279 link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/8751561 PubMed]
+
# Ball HG, Blessing JA, Lentz SS, Mutch DG. 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/abstract link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/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. [http://annonc.oxfordjournals.org/content/7/8/861.long link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/8922203 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. [http://annonc.oxfordjournals.org/content/7/8/861.long link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/8922203 PubMed]
# Lincoln S, Blessing JA, Lee RB, Rocereto TF. 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.sciencedirect.com/science/article/pii/S0090825802000689 link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/12648575 PubMed]
+
# Lincoln S, Blessing JA, Lee RB, Rocereto TF. 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/abstract link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/12648575 PubMed]
  
 
==Temsirolimus (Torisel) {{#subobject:c19c6|Regimen=1}}==
 
==Temsirolimus (Torisel) {{#subobject:c19c6|Regimen=1}}==
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|[[#toc|back to top]]
 
|[[#toc|back to top]]
 
|}
 
|}
===Regimen, Oza et al. 2011 {{#subobject:53c722|Variant=1}}===
+
===Regimen {{#subobject:53c722|Variant=1}}===
Level of Evidence:
+
{| border="1" style="text-align:center;" !align="left"
<span  
+
|'''Study'''
 +
|[[Levels_of_Evidence#Evidence|'''Evidence''']]
 +
|-
 +
|[http://jco.ascopubs.org/content/29/24/3278.long Oza et al. 2011]
 +
|<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;
 
padding:3px 6px 3px 6px;
 
padding:3px 6px 3px 6px;
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border-width:2px;
 
border-width:2px;
 
border-style:solid;">Phase II</span>
 
border-style:solid;">Phase II</span>
 
+
|-
 +
|}
 +
====Chemotherapy====
 
*[[Temsirolimus (Torisel)]] 25 mg IV over 30 minutes once per day on days 1, 8, 15, 22
 
*[[Temsirolimus (Torisel)]] 25 mg IV over 30 minutes once per day on days 1, 8, 15, 22
  
Line 724: Line 827:
  
 
===References===
 
===References===
# 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. 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. doi: 10.1200/JCO.2010.34.1578. Epub 2011 Jul 25. [http://jco.ascopubs.org/content/29/24/3278.long link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/21788564 PubMed]
+
# 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. 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. [http://jco.ascopubs.org/content/29/24/3278.long link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/21788564 PubMed]
  
 
==Topotecan (Hycamtin) {{#subobject:9a02a0|Regimen=1}}==
 
==Topotecan (Hycamtin) {{#subobject:9a02a0|Regimen=1}}==
Line 732: Line 835:
 
|}
 
|}
 
===Regimen {{#subobject:1c2f98|Variant=1}}===
 
===Regimen {{#subobject:1c2f98|Variant=1}}===
Level of Evidence:
+
{| border="1" style="text-align:center;" !align="left"
<span  
+
|'''Study'''
 +
|[[Levels_of_Evidence#Evidence|'''Evidence''']]
 +
|-
 +
|[http://jco.ascopubs.org/content/21/11/2110.long Wadler et al. 2003 (ECOG E3E93)]
 +
|<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;
 
padding:3px 6px 3px 6px;
 
padding:3px 6px 3px 6px;
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border-width:2px;
 
border-width:2px;
 
border-style:solid;">Phase II</span>
 
border-style:solid;">Phase II</span>
 
+
|-
*[[Topotecan (Hycamtin)]] 1.5 mg/m2 IV once per day on days 1 to 5
+
|}
**Dosage for patients with previous pelvic radiation is [[Topotecan (Hycamtin)]] 1.2 mg/m2, which can be increase to the 1.5 mg/m2 dose in later cycles if there are no toxicities higher than grade 1
+
====Chemotherapy====
 +
*[[Topotecan (Hycamtin)]] 1.5 mg/m<sup>2</sup> IV once per day on days 1 to 5
 +
**Dosage for patients with previous pelvic radiation is 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
  
 
'''21-day cycles'''
 
'''21-day cycles'''
Line 768: Line 877:
 
border-style:solid;">Phase III</span>
 
border-style:solid;">Phase III</span>
 
|[[Uterine_cancer#Cisplatin_.26_Doxorubicin|Cisplatin & Doxorubicin]]
 
|[[Uterine_cancer#Cisplatin_.26_Doxorubicin|Cisplatin & Doxorubicin]]
|-
 
!colspan="4" align="center"|
 
 
|-
 
|-
 
|[http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2752331 Wolfson et al. 2007 (GOG 150)]
 
|[http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2752331 Wolfson et al. 2007 (GOG 150)]

Revision as of 21:07, 21 August 2016

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Is there a regimen missing from this list? Would you like to share a different dosage/schedule or an additional reference for a regimen? Have you noticed an error? Do you have an idea that will help the site grow to better meet your needs and the needs of many others? You are invited to contribute to the site.

35 regimens on this page
55 variants on this page


Endocrine therapy for endometrioid histologies

Anastrozole (Arimidex)

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Regimen

Study Evidence
Rose et al. 2000 Phase II

Endocrine therapy

given until progression of disease or unacceptable toxicity

References

  1. Rose PG, Brunetto VL, VanLe L, Bell J, Walker JL, Lee RB. 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 verified protocol PubMed

Medroxyprogesterone acetate (MPA)

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Regimen

Study Evidence Comparator
Thigpen et al. 1999 Phase III High-dose medroxyprogesterone acetate

Endocrine therapy

Given until progression of disease or unacceptable toxicity

References

  1. Thigpen JT, Brady MF, Alvarez RD, Adelson MD, Homesley HD, Manetta A, Soper JT, Given FT. 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 verified protocol PubMed

Medroxyprogesterone acetate & Tamoxifen

back to top

Regimen

Study Evidence
Whitney et al. 2004 Phase II

Endocrine therapy

Given until progression of disease or unacceptable toxicity

References

  1. Whitney CW, Brunetto VL, Zaino RJ, Lentz SS, Sorosky J, Armstrong DK, Lee RB; Gynecologic Oncology Group study. 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 verified protocol PubMed

Megestrol acetate (Megace)

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Regimen

Study Evidence Comparator
Pandya et al. 2001 (E4882) Randomized Phase II Megestrol acetate & Tamoxifen

Endocrine therapy

Given until progression of disease or unacceptable toxicity

References

  1. 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 verified protocol PubMed

Megestrol acetate & Tamoxifen

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Regimen

Study Evidence Comparator
Pandya et al. 2001 (E4882) Randomized Phase II Megestrol acetate

Endocrine therapy

3-week courses of Megestrol acetate (Megace), alternating back and forth with 3-week courses of Tamoxifen (Nolvadex); given until progression of disease or unacceptable toxicity

References

  1. 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 verified protocol PubMed
  2. Fiorica JV, Brunetto VL, Hanjani P, Lentz SS, Mannel R, Andersen W; Gynecologic Oncology Group study. 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 verified protocol PubMed

Tamoxifen (Nolvadex)

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Regimen

Study Evidence
Quinn et al. 1989 Phase II
Thigpen et al. 2001 Phase II

Endocrine therapy

Given until progression of disease or unacceptable toxicity

References

  1. Quinn MA, Campbell JJ. Tamoxifen therapy in advanced/recurrent endometrial carcinoma. Gynecol Oncol. 1989 Jan;32(1):1-3. link to SD article PubMed
  2. 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 verified protocol PubMed

Adjuvant radiation & chemotherapy

RT -> Cisplatin & Doxorubicin

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RT: Radiation Therapy

Regimen

Study Evidence Comparator
Homesley et al. 2008 (GOG 184) Phase III Cisplatin, Doxorubicin, Paclitaxel, RT

Note: for chemotherapy, body surface area capped at 2.0 m2. Radiation is to begin within 8 weeks after surgery.

Radiotherapy

  • Radiation therapy to the pelvis, 1.8 Gy x 28 fractions (total dose: 50.4 Gy)
    • Patients with positive para-aortic lymph nodes received 1.5 to 1.8 Gy x 24 to 29 fractions (total dose: 43.5 Gy)

6-week course, followed within 8 weeks by:

Chemotherapy

Supportive medications

21-day cycle for 6 cycles

References

  1. 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 link to PMC article contains verified protocol PubMed

RT -> Cisplatin, Doxorubicin, Paclitaxel

back to top

RT: Radiation Therapy

Regimen

Study Evidence Comparator
Homesley et al. 2008 (GOG 184) Phase III Cisplatin, Doxorubicin, RT

Note: for chemotherapy, body surface area capped at 2.0 m2. Radiation is to start within 8 weeks after surgery.

Radiotherapy

  • Radiation therapy to the pelvis, 1.8 Gy x 28 fractions (total dose: 50.4 Gy)
    • Patients with positive para-aortic lymph nodes received 1.5 to 1.8 Gy x 24 to 29 fractions (total dose: 43.5 Gy)

6-week course, followed within 8 weeks by:

Chemotherapy

Supportive medications

21-day cycle for 6 cycles

References

  1. 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 link to PMC article contains verified protocol PubMed

Advanced, recurrent, or metastatic disease

Bevacizumab (Avastin)

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Regimen

Study Evidence
Aghajanian et al. 2011 Phase II

Chemotherapy

21-day cycles, given until progression of disease or unacceptable toxicity

References

  1. Aghajanian C, Sill MW, Darcy KM, Greer B, McMeekin DS, Rose PG, Rotmensch J, Barnes MN, Hanjani P, Leslie KK. 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 verified protocol PubMed

Carboplatin (Paraplatin)

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Regimen

Study Evidence
van Wijk et al. 2003 Phase II

Chemotherapy

28-day cycles

References

  1. van Wijk FH, Lhommé C, Bolis G, Scotto di Palumbo V, Tumolo S, Nooij M, de Oliveira CF, Vermorken JB; European Organization for Research and Treatment of Cancer. 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 verified protocol PubMed

Carboplatin & Doxorubicin liposomal

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Regimen

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

Chemotherapy

Supportive medications

  • "No prophylactic use of G-CSF was recommended. In case of grade 4 neutropaenia, even without fever, therapeutic and prophylactic use of G-CSF was allowed."

28-day cycle for 3 to 6 cycles

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

References

  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 PMC article contains verified protocol PubMed

Carboplatin & Paclitaxel

back to top

Regimen #1

Study Evidence
Pectasides et al. 2008 Phase II

Chemotherapy

21-day cycle for 6 to 9 cycles

Regimen #2

Study Evidence
Hoskins et al. 2001 Phase II

Chemotherapy

21-day cycles

Regimen #3

Study Evidence
Sorbe et al. 2008 Phase II

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 verified protocol PubMed
  2. 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 verified protocol PubMed content property of HemOnc.org
  3. 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 verified protocol PubMed
  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

Cisplatin & Doxorubicin

back to top

Regimen #1

Study Evidence Comparator
Fleming et al. 2004 (GOG 177) Phase III Cisplatin, Doxorubicin, Paclitaxel

Note: body surface area capped at 2.0 m2.

Chemotherapy

21-day cycle for 7 cycles

Regimen #2

Study Evidence Comparator
Randall et al. 2006 (GOG 122) Phase III Whole abdominal irradiation

Chemotherapy

Supportive hydration:

  • Normal saline at 500 mL/H for 2 hours prior to and after cisplatin

21-day cycle for 8 cycles

References

  1. 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 verified protocol PubMed
  2. Randall ME, Filiaci VL, Muss H, Spirtos NM, Mannel RS, Fowler J, Thigpen JT, Benda JA; Gynecologic Oncology Group Study. 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 verified protocol PubMed

Cisplatin, Doxorubicin, Paclitaxel

back to top

Regimen

Study Evidence Comparator
Fleming et al. 2004 (GOG 177) Phase III Cisplatin & Doxorubicin

Note: body surface area capped at 2.0 m2.

Chemotherapy

Supportive medications

21-day cycle for 7 cycles

References

  1. 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 verified protocol PubMed

Cisplatin, Ifosfamide, Mesna (CIM)

back to top

CIM: Cisplatin, Ifosfamide, Mesna

Regimen

Study Evidence Comparator
Wolfson et al. 2007 (GOG 150) Phase III Whole abdominal irradiation

Chemotherapy

Supportive medications

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

21-day cycle for 3 cycles

References

  1. 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 PMC article contains verified protocol PubMed

Cisplatin & Paclitaxel

back to top

Regimen

Study Evidence
Dimopoulos et al. 2000 Phase II

Chemotherapy

Supportive medications

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 verified protocol PubMed

Dactinomycin (Cosmegen)

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Regimen

Study Evidence
Moore et al. 1999 Phase II

Chemotherapy

28-day cycles

References

  1. Moore DH, Blessing JA, Dunton C, Buller RE, Reid GC. 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 verified protocol PubMed

Ifosfamide

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Regimen

Study Evidence Comparator
Homesley et al. 2007 (GOG 161) Phase III Ifosfamide & Paclitaxel

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

Supportive medications

  • Mesna (Mesnex) 2000 mg IV over 12 hours once per day on days 1 to 3, starting 15 minutes before Ifosfamide (Ifex)
    • Alternate PO dosing: Mesna (Mesnex) 1330 mg PO taken three times per day, 1 hour before, 4 hours after, and 8 hours after Ifosfamide (Ifex) (4000 mg total dose per day), on days 1 to 3
  • Filgrastim (Neupogen) 5 mcg/kg SC once per day starting on day 4, to continue until ANC is greater than or equal to 2000

21-day cycle for 8 cycles

References

  1. 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 verified protocol PubMed

Ifosfamide & Paclitaxel

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Regimen

Study Evidence Comparator
Homesley et al. 2007 (GOG 161) Phase III Ifosfamide

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

Supportive medications

21-day cycle for 8 cycles

References

  1. 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 verified protocol PubMed

Paclitaxel (Taxol)

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Regimen #1

Study Evidence
Lincoln et al. 2003 Phase II

Chemotherapy

Supportive medications

  • Dexamethasone (Decadron) 20 mg PO/IV given twice, 12 and 6 hours prior to paclitaxel
  • Diphenhydramine (Benadryl) 50 mg PO/IV once 30 minutes prior to paclitaxel
  • Cimetidine (Tagamet) 300 mg IV once 30 minutes prior to paclitaxel

21-day cycles

Regimen #2

Study Evidence
Lissoni et al. 1996 Phase II

Chemotherapy

Supportive medications

  • Hydrocortisone (Cortef) 250 mg IV once 1 hour prior to paclitaxel
  • Chlorphenamine/chlorpheniramine (H1 blocker) 10 mg IM once 1 hour prior to paclitaxel
  • Cimetidine (Tagamet) 300 mg IV once 1 hour prior to paclitaxel

21-day cycles

Regimen #3

Study Evidence
Ball et al. 1996 Phase II

Chemotherapy

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

Supportive medications

  • Dexamethasone (Decadron) 20 mg PO/IV given twice, 12 and 6 hours prior to paclitaxel
  • Diphenhydramine (Benadryl) 50 mg PO/IV once 30 minutes prior to paclitaxel
  • Cimetidine (Tagamet) 300 mg IV once 30 minutes prior to paclitaxel
  • Filgrastim (Neupogen) 5 mcg/kg SC once per day starting on day 3, 24 hours after chemotherapy, continued for at least 12 days or until two successive total leukocyte counts are 10,000 or greater, whichever comes last

21-day cycles

References

  1. Ball HG, Blessing JA, Lentz SS, Mutch DG. 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 verified protocol 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 verified protocol PubMed
  3. Lincoln S, Blessing JA, Lee RB, Rocereto TF. 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 verified protocol PubMed

Temsirolimus (Torisel)

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Regimen

Study Evidence
Oza et al. 2011 Phase II

Chemotherapy

28-day cycles, given until progression of disease, unacceptable toxicity, or patient decision

References

  1. 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. 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 verified protocol PubMed

Topotecan (Hycamtin)

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Regimen

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

Chemotherapy

  • Topotecan (Hycamtin) 1.5 mg/m2 IV once per day on days 1 to 5
    • Dosage for patients with previous pelvic radiation is 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. 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 verified protocol PubMed

Whole abdominal radiation (WAI)

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Regimen

Study Evidence Comparator
Randall et al. 2006 (GOG 122) Phase III Cisplatin & Doxorubicin
Wolfson et al. 2007 (GOG 150) Phase III CIM

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

References

  1. Randall ME, Filiaci VL, Muss H, Spirtos NM, Mannel RS, Fowler J, Thigpen JT, Benda JA; Gynecologic Oncology Group Study. 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 verified protocol PubMed
  2. 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 PMC article contains verified protocol PubMed