Neoadjuvant–Adjuvant or Adjuvant-Only Pembrolizumab in Advanced Melanoma

医学 彭布罗利珠单抗 辅助治疗 佐剂 新辅助治疗 外科 黑色素瘤 临床终点 人口 内科学 肿瘤科 随机对照试验 癌症 化疗 乳腺癌 免疫疗法 癌症研究 环境卫生
作者
Sapna Patel,Megan Othus,Yuanbin Chen,G. Paul Wright,Kathleen J. Yost,John Hyngstrom,Siwen Hu-Lieskovan,Christopher D. Lao,Leslie A. Fecher,Thach-Giao Truong,Jennifer L Eisenstein,Sunandana Chandra,Jeffrey A. Sosman,Kari Kendra,Richard C. Wu,Craig Devoe,Gary B. Deutsch,Aparna Hegde,Maya Khalil,Ankit Mangla,Amy M Reese,Merrick I. Ross,Andrew Poklepovic,Giao Q. Phan,Adedayo A. Onitilo,Demet G Yasar,Benjamin Powers,Gary C. Doolittle,Gino K. In,Niels Kokot,Geoffrey T. Gibney,Michael B. Atkins,Montaser Shaheen,James Warneke,Alexandra Ikeguchi,Jose E Najera,Bartosz Chmielowski,Joseph G. Crompton,Justin D. Floyd,Eddy C. Hsueh,Kim Margolin,Warren Chow,K Grossmann,Eliana Dietrich,Victor G. Prieto,Michael C. Lowe,Elizabeth I. Buchbinder,John M. Kirkwood,Larissa A. Korde,James Moon,Elad Sharon,Vernon K. Sondak,Antoni Ribas
出处
期刊:The New England Journal of Medicine [New England Journal of Medicine]
卷期号:388 (9): 813-823 被引量:36
标识
DOI:10.1056/nejmoa2211437
摘要

Whether pembrolizumab given both before surgery (neoadjuvant therapy) and after surgery (adjuvant therapy), as compared with pembrolizumab given as adjuvant therapy alone, would increase event-free survival among patients with resectable stage III or IV melanoma is unknown. Download a PDF of the Research Summary. In a phase 2 trial, we randomly assigned patients with clinically detectable, measurable stage IIIB to IVC melanoma that was amenable to surgical resection to three doses of neoadjuvant pembrolizumab, surgery, and 15 doses of adjuvant pembrolizumab (neoadjuvant–adjuvant group) or to surgery followed by pembrolizumab (200 mg intravenously every 3 weeks for a total of 18 doses) for approximately 1 year or until disease recurred or unacceptable toxic effects developed (adjuvant-only group). The primary end point was event-free survival in the intention-to-treat population. Events were defined as disease progression or toxic effects that precluded surgery; the inability to resect all gross disease; disease progression, surgical complications, or toxic effects of treatment that precluded the initiation of adjuvant therapy within 84 days after surgery; recurrence of melanoma after surgery; or death from any cause. Safety was also evaluated. At a median follow-up of 14.7 months, the neoadjuvant–adjuvant group (154 patients) had significantly longer event-free survival than the adjuvant-only group (159 patients) (P=0.004 by the log-rank test). In a landmark analysis, event-free survival at 2 years was 72% (95% confidence interval [CI], 64 to 80) in the neoadjuvant–adjuvant group and 49% (95% CI, 41 to 59) in the adjuvant-only group. The percentage of patients with treatment-related adverse events of grades 3 or higher during therapy was 12% in the neoadjuvant–adjuvant group and 14% in the adjuvant-only group. Among patients with resectable stage III or IV melanoma, event-free survival was significantly longer among those who received pembrolizumab both before and after surgery than among those who received adjuvant pembrolizumab alone. No new toxic effects were identified. (Funded by the National Cancer Institute and Merck Sharp and Dohme; S1801 ClinicalTrials.gov number, NCT03698019.) QUICK TAKE VIDEO SUMMARYNeoadjuvant Pembrolizumab for Advanced Melanoma 02:13
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