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Adjuvant Pembrolizumab after Nephrectomy in Renal-Cell Carcinoma

医学 危险系数 彭布罗利珠单抗 肾细胞癌 肾切除术 安慰剂 临床终点 中期分析 外科 辅助治疗 不利影响 随机化 内科学 置信区间 泌尿科 免疫疗法 随机对照试验 癌症 病理 替代医学
作者
Toni K. Choueiri,Piotr Tomczak,Se Hoon Park,Balaji Venugopal,Thomas Ferguson,Yen‐Hwa Chang,Jaroslav Hájek,Stefan N. Symeonides,Jae‐Lyun Lee,Naveed Sarwar,Antoine Thiery-Vuillemin,Marine Gross‐Goupil,Mauricio Mahave,Naomi B. Haas,Piotr Sawrycki,Howard Gurney,Christine Chevreau,Bohuslav Melichar,Evgeniy Kopyltsov,Ajjai Alva,John M. Burke,Gurjyot K. Doshi,Delphine Topart,Stéphane Oudard,Hans J. Hammers,Hiroshi Kitamura,Jens Bedke,Rodolfo F. Perini,Pingye Zhang,Kazuo Imai,Jaqueline Willemann-Rogerio,David I. Quinn,Thomas Powles
出处
期刊:The New England Journal of Medicine [New England Journal of Medicine]
卷期号:385 (8): 683-694 被引量:463
标识
DOI:10.1056/nejmoa2106391
摘要

Patients with renal-cell carcinoma who undergo nephrectomy have no options for adjuvant therapy to reduce the risk of recurrence that have high levels of supporting evidence.In a double-blind, phase 3 trial, we randomly assigned, in a 1:1 ratio, patients with clear-cell renal-cell carcinoma who were at high risk for recurrence after nephrectomy, with or without metastasectomy, to receive either adjuvant pembrolizumab (at a dose of 200 mg) or placebo intravenously once every 3 weeks for up to 17 cycles (approximately 1 year). The primary end point was disease-free survival according to the investigator's assessment. Overall survival was a key secondary end point. Safety was a secondary end point.A total of 496 patients were randomly assigned to receive pembrolizumab, and 498 to receive placebo. At the prespecified interim analysis, the median time from randomization to the data-cutoff date was 24.1 months. Pembrolizumab therapy was associated with significantly longer disease-free survival than placebo (disease-free survival at 24 months, 77.3% vs. 68.1%; hazard ratio for recurrence or death, 0.68; 95% confidence interval [CI], 0.53 to 0.87; P = 0.002 [two-sided]). The estimated percentage of patients who remained alive at 24 months was 96.6% in the pembrolizumab group and 93.5% in the placebo group (hazard ratio for death, 0.54; 95% CI, 0.30 to 0.96). Grade 3 or higher adverse events of any cause occurred in 32.4% of the patients who received pembrolizumab and in 17.7% of those who received placebo. No deaths related to pembrolizumab therapy occurred.Pembrolizumab treatment led to a significant improvement in disease-free survival as compared with placebo after surgery among patients with kidney cancer who were at high risk for recurrence. (Funded by Merck Sharp and Dohme, a subsidiary of Merck; KEYNOTE-564 ClinicalTrials.gov number, NCT03142334.).
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