Pembrolizumab versus placebo as adjuvant therapy in resected stage IIB or IIC melanoma: Long-term follow-up, crossover, and rechallenge with pembrolizumab in the phase III KEYNOTE-716 study

IF 7.6 1区 医学 Q1 ONCOLOGY
Jason J. Luke , Paolo A. Ascierto , Muhammad A. Khattak , Piotr Rutkowski , Michele Del Vecchio , Francesco Spagnolo , Jacek Mackiewicz , Luis de la Cruz Merino , Vanna Chiarion-Sileni , John M. Kirkwood , Caroline Robert , Dirk Schadendorf , Federica de Galitiis , Matteo S. Carlino , Reinhard Dummer , Peter Mohr , Amos Odeleye-Ajakaye , Mizuho Fukunaga-Kalabis , Clemens Krepler , Alexander M.M. Eggermont , Georgina V. Long
{"title":"Pembrolizumab versus placebo as adjuvant therapy in resected stage IIB or IIC melanoma: Long-term follow-up, crossover, and rechallenge with pembrolizumab in the phase III KEYNOTE-716 study","authors":"Jason J. Luke ,&nbsp;Paolo A. Ascierto ,&nbsp;Muhammad A. Khattak ,&nbsp;Piotr Rutkowski ,&nbsp;Michele Del Vecchio ,&nbsp;Francesco Spagnolo ,&nbsp;Jacek Mackiewicz ,&nbsp;Luis de la Cruz Merino ,&nbsp;Vanna Chiarion-Sileni ,&nbsp;John M. Kirkwood ,&nbsp;Caroline Robert ,&nbsp;Dirk Schadendorf ,&nbsp;Federica de Galitiis ,&nbsp;Matteo S. Carlino ,&nbsp;Reinhard Dummer ,&nbsp;Peter Mohr ,&nbsp;Amos Odeleye-Ajakaye ,&nbsp;Mizuho Fukunaga-Kalabis ,&nbsp;Clemens Krepler ,&nbsp;Alexander M.M. Eggermont ,&nbsp;Georgina V. Long","doi":"10.1016/j.ejca.2025.115381","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>Adjuvant pembrolizumab prolonged recurrence-free survival (RFS) and distant metastasis-free survival (DMFS) in patients with resected stage IIB/IIC melanoma in KEYNOTE-716. Results of a post hoc 4-year analysis are reported, including progression/recurrence-free survival 2 (PRFS2).</div></div><div><h3>Methods</h3><div>Patients were randomly assigned 1:1 to pembrolizumab 200 mg or placebo intravenously every 3 weeks (part 1). RFS was the primary end point; DMFS was secondary. Patients with recurrence following placebo or 17 cycles of pembrolizumab could cross over to or be rechallenged with pembrolizumab (part 2).</div></div><div><h3>Results</h3><div>Median follow-up (n = 976) was 52.8 months (range, 39.4–64.8). RFS (HR, 0.62 [95 % CI, 0.50–0.78]) and DMFS (HR, 0.59 [0.45–0.77]) favored pembrolizumab. At 48 months, RFS rates were 71.3 % for pembrolizumab and 58.3 % for placebo, and DMFS rates were 81.0 % and 70.1 %, respectively. The HR for PRFS2 was 0.75 (95 % CI, 0.56–1.01); 48-month PRFS2 rates were 82.5 % for pembrolizumab and 76.7 % for placebo. In the crossover population, median follow-up was 36.9 months; median RFS was not reached (NR; 95 % CI, 16.8-NR; 48-month RFS, 50.6 %) in patients with resectable disease (n = 41) and median progression-free survival was 22.0 months (4.5-NR) in patients with unresectable disease (n = 30). Among patients rechallenged, median follow-up was 21.9 months; none with resectable disease had recurrence (n = 6) and 1 with unresectable disease had best response of stable disease (n = 3). No new safety signals were observed.</div></div><div><h3>Conclusions</h3><div>With &gt; 4 years follow-up, pembrolizumab continued to prolong RFS and DMFS and had antitumor activity in patients who crossed over to pembrolizumab.</div><div>Trial registration: NCT03553836</div></div>","PeriodicalId":11980,"journal":{"name":"European Journal of Cancer","volume":"220 ","pages":"Article 115381"},"PeriodicalIF":7.6000,"publicationDate":"2025-03-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Cancer","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0959804925001625","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background

Adjuvant pembrolizumab prolonged recurrence-free survival (RFS) and distant metastasis-free survival (DMFS) in patients with resected stage IIB/IIC melanoma in KEYNOTE-716. Results of a post hoc 4-year analysis are reported, including progression/recurrence-free survival 2 (PRFS2).

Methods

Patients were randomly assigned 1:1 to pembrolizumab 200 mg or placebo intravenously every 3 weeks (part 1). RFS was the primary end point; DMFS was secondary. Patients with recurrence following placebo or 17 cycles of pembrolizumab could cross over to or be rechallenged with pembrolizumab (part 2).

Results

Median follow-up (n = 976) was 52.8 months (range, 39.4–64.8). RFS (HR, 0.62 [95 % CI, 0.50–0.78]) and DMFS (HR, 0.59 [0.45–0.77]) favored pembrolizumab. At 48 months, RFS rates were 71.3 % for pembrolizumab and 58.3 % for placebo, and DMFS rates were 81.0 % and 70.1 %, respectively. The HR for PRFS2 was 0.75 (95 % CI, 0.56–1.01); 48-month PRFS2 rates were 82.5 % for pembrolizumab and 76.7 % for placebo. In the crossover population, median follow-up was 36.9 months; median RFS was not reached (NR; 95 % CI, 16.8-NR; 48-month RFS, 50.6 %) in patients with resectable disease (n = 41) and median progression-free survival was 22.0 months (4.5-NR) in patients with unresectable disease (n = 30). Among patients rechallenged, median follow-up was 21.9 months; none with resectable disease had recurrence (n = 6) and 1 with unresectable disease had best response of stable disease (n = 3). No new safety signals were observed.

Conclusions

With > 4 years follow-up, pembrolizumab continued to prolong RFS and DMFS and had antitumor activity in patients who crossed over to pembrolizumab.
Trial registration: NCT03553836
Pembrolizumab与安慰剂作为切除的IIB或IIC期黑色素瘤的辅助治疗:在III期KEYNOTE-716研究中,Pembrolizumab的长期随访,交叉和再挑战
KEYNOTE-716中,pembrolizumab佐剂延长了IIB/IIC期黑色素瘤切除患者的无复发生存期(RFS)和无远处转移生存期(DMFS)。报告了一项为期4年的事后分析结果,包括无进展/复发生存期2 (PRFS2)。方法将患者按1:1的比例随机分配至每3周静脉注射一次派姆单抗200 mg或安慰剂组(第一部分)。DMFS是次要的。在安慰剂或17个周期的派姆单抗治疗后复发的患者可以交叉使用或再次使用派姆单抗(第2部分)。结果中位随访(n = 976)为52.8个月(范围,39.4-64.8)。RFS (HR, 0.62[95 % CI, 0.50-0.78])和DMFS (HR, 0.59[0.45-0.77])有利于派姆单抗。在48个月时,派姆单抗的RFS率为71.3 %,安慰剂为58.3 %,DMFS率分别为81.0 %和70.1 %。PRFS2的HR为0.75(95 % CI, 0.56-1.01);派姆单抗组48个月PRFS2率为82.5 %,安慰剂组为76.7 %。在交叉人群中,中位随访时间为36.9个月;中位RFS未达到(NR;95 % ci, 16.8-nr;可切除疾病患者的48个月RFS(50.6 %)(n = 41),不可切除疾病患者的中位无进展生存期为22.0个月(4.5 nr) (n = 30)。重新挑战的患者中位随访时间为21.9个月;可切除的疾病无复发(n = 6),不可切除的疾病1例病情稳定,疗效最佳(n = 3)。没有观察到新的安全信号。结论>; 随访4年,派姆单抗继续延长RFS和DMFS,并且在交叉使用派姆单抗的患者中具有抗肿瘤活性。试验注册:NCT03553836
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
European Journal of Cancer
European Journal of Cancer 医学-肿瘤学
CiteScore
11.50
自引率
4.80%
发文量
953
审稿时长
23 days
期刊介绍: The European Journal of Cancer (EJC) serves as a comprehensive platform integrating preclinical, digital, translational, and clinical research across the spectrum of cancer. From epidemiology, carcinogenesis, and biology to groundbreaking innovations in cancer treatment and patient care, the journal covers a wide array of topics. We publish original research, reviews, previews, editorial comments, and correspondence, fostering dialogue and advancement in the fight against cancer. Join us in our mission to drive progress and improve outcomes in cancer research and patient care.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信