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m (Replaced content with "==Carboplatin & Paclitaxel (CP) & Nivolumab {{#subobject:3a6hg7|Regimen=1}}== CP & Nivolumab: '''<u>C</u>'''arboplatin, '''<u>P</u>'''aclitaxel, Nivolumab <div class="tocc...")
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==Carboplatin & RT {{#subobject:ea866d|Regimen=1}}==
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==Carboplatin & Paclitaxel (CP) & Nivolumab {{#subobject:3a6hg7|Regimen=1}}==
Carboplatin & RT: Carboplatin & '''<u>R</u>'''adiation '''<u>T</u>'''herapy
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CP & Nivolumab: '''<u>C</u>'''arboplatin, '''<u>P</u>'''aclitaxel, Nivolumab
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen variant #1, weekly carboplatin {{#subobject:e0ewe0|Variant=1}}===
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===Regimen variant #1, 5/175/360 {{#subobject:59hhq7|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
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!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(23)00479-5 Monk et al. 2023 (CALLA)]
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|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9844511/ Forde et al. 2022 (CheckMate 816)]
|2019-02-15 to 2020-12-10
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{| class="wikitable" style="margin:auto; color:black; background-color:#d3d3d3"
|style="background-color:#1a9851"|Phase 3 (C)
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|[[File:HopeAI.png|link=https://hemonc.org|alt=Alt text|Title=text|frameless|150px|center]]
|1a. [[#Carboplatin.2C_Durvalumab.2C_RT_999|Carboplatin, Durvalumab, RT]]<br>1b. [[#Cisplatin.2C_Durvalumab.2C_RT_999|Cisplatin, Durvalumab, RT]]
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|-
| style="background-color:#ffffbf" |Did not meet primary endpoint of PFS
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|Click to learn more!
 +
|-
 +
|}
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|2017-2019
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| style="background-color:#1a9851" |Phase 3 (E-RT-esc)
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|1a. [[#Carboplatin_.26_Paclitaxel_.28CP.29|CP]]<br>1b. [[#Cisplatin_.26_Vinorelbine_.28CVb.29|CVb]]<br>1c. [[#Cisplatin_.26_Docetaxel_.28DC.29|DC]]
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| style="background-color:#1a9850" |Superior EFS (co-primary endpoint)<br>Median EFS: 31.6 vs 20.8 mo<br>(HR 0.63, 97.38% CI 0.43-0.91)<br><br>Superior pCR rate (co-primary endpoint)<br>pCR rate: 24% vs 2.2%<br>(OR 13.94, 99% CI 3.49-55.75)
 
|-
 
|-
 
|}
 
|}
<div class="toccolours" style="background-color:#b3e2cd">
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''Note: there were additional comparator options depending on histology; see the respective histology-specific pages for more details.''
====Chemotherapy====
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<div class="toccolours" style="background-color:#fdcdac">
*[[Carboplatin (Paraplatin)]] AUC 2 IV once per day on days 1, 8, 15, 22, 29
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====Biomarker eligibility criteria====
====Radiotherapy====
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*CheckMate 816: No sensitizing EGFR or ALK mutations
*Concurrent [[External_beam_radiotherapy|radiation therapy]], 1.8 Gy per fraction on days 1 to 5, 8 to 12, 15 to 19, 22 to 26, 29 to 33 (45 Gy total in 25 fractions)
 
'''5-week course'''
 
</div>
 
<div class="toccolours" style="background-color:#cbd5e8">
 
====Subsequent treatment====
 
*Brachytherapy
 
 
</div></div>
 
</div></div>

Latest revision as of 12:58, 18 July 2024

Carboplatin & Paclitaxel (CP) & Nivolumab

CP & Nivolumab: Carboplatin, Paclitaxel, Nivolumab

Regimen variant #1, 5/175/360

Study Dates of enrollment Evidence Comparator Comparative Efficacy
Forde et al. 2022 (CheckMate 816)
Alt text
Click to learn more!
2017-2019 Phase 3 (E-RT-esc) 1a. CP
1b. CVb
1c. DC
Superior EFS (co-primary endpoint)
Median EFS: 31.6 vs 20.8 mo
(HR 0.63, 97.38% CI 0.43-0.91)

Superior pCR rate (co-primary endpoint)
pCR rate: 24% vs 2.2%
(OR 13.94, 99% CI 3.49-55.75)

Note: there were additional comparator options depending on histology; see the respective histology-specific pages for more details.

Biomarker eligibility criteria

  • CheckMate 816: No sensitizing EGFR or ALK mutations