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Nivolumab plus Cabozantinib versus Sunitinib for Advanced Renal-Cell Carcinoma

舒尼替尼 卡波扎尼布 医学 无容量 肾细胞癌 危险系数 内科学 临床终点 索拉非尼 肿瘤科 肾癌 无进展生存期 泌尿科 置信区间 伦瓦提尼 外科 胃肠病学 酪氨酸激酶抑制剂 癌症研究 阿西替尼 不利影响 随机对照试验 癌症 总体生存率 免疫疗法
作者
Toni K. Choueiri,Peter Schmid,Mauricio Burotto,Bernard Escudier,María Teresa Bourlon,Bogdan Żurawski,Victor Manuel Oyervides Juárez,James J. Hsieh,Umberto Basso,Amishi Yogesh Shah,Cristina Suárez,Alketa Hamzaj,Jeffrey C. Goh,Carlos H. Barrios,Martin Eduardo Richardet,Camillo Porta,Rubén Dario Kowalyszyn,Juan P. Feregrino,Jakub Żołnierek,David Pook,Elizabeth R. Kessler,Yoshihiko Tomita,Ryuichi Mizuno,Jens Bedke,Joshua Zhang,Matthew Maurer,Burçin Şimşek,Flavia Ejzykowicz,Gisela Schwab,Andrea B. Apolo,Robert J. Motzer
出处
期刊:The New England Journal of Medicine [New England Journal of Medicine]
卷期号:384 (9): 829-841 被引量:844
标识
DOI:10.1056/nejmoa2026982
摘要

The efficacy and safety of nivolumab plus cabozantinib as compared with those of sunitinib in the treatment of previously untreated advanced renal-cell carcinoma are not known.In this phase 3, randomized, open-label trial, we randomly assigned adults with previously untreated clear-cell, advanced renal-cell carcinoma to receive either nivolumab (240 mg every 2 weeks) plus cabozantinib (40 mg once daily) or sunitinib (50 mg once daily for 4 weeks of each 6-week cycle). The primary end point was progression-free survival, as determined by blinded independent central review. Secondary end points included overall survival, objective response as determined by independent review, and safety. Health-related quality of life was an exploratory end point.Overall, 651 patients were assigned to receive nivolumab plus cabozantinib (323 patients) or sunitinib (328 patients). At a median follow-up of 18.1 months for overall survival, the median progression-free survival was 16.6 months (95% confidence interval [CI], 12.5 to 24.9) with nivolumab plus cabozantinib and 8.3 months (95% CI, 7.0 to 9.7) with sunitinib (hazard ratio for disease progression or death, 0.51; 95% CI, 0.41 to 0.64; P<0.001). The probability of overall survival at 12 months was 85.7% (95% CI, 81.3 to 89.1) with nivolumab plus cabozantinib and 75.6% (95% CI, 70.5 to 80.0) with sunitinib (hazard ratio for death, 0.60; 98.89% CI, 0.40 to 0.89; P = 0.001). An objective response occurred in 55.7% of the patients receiving nivolumab plus cabozantinib and in 27.1% of those receiving sunitinib (P<0.001). Efficacy benefits with nivolumab plus cabozantinib were consistent across subgroups. Adverse events of any cause of grade 3 or higher occurred in 75.3% of the 320 patients receiving nivolumab plus cabozantinib and in 70.6% of the 320 patients receiving sunitinib. Overall, 19.7% of the patients in the combination group discontinued at least one of the trial drugs owing to adverse events, and 5.6% discontinued both. Patients reported better health-related quality of life with nivolumab plus cabozantinib than with sunitinib.Nivolumab plus cabozantinib had significant benefits over sunitinib with respect to progression-free survival, overall survival, and likelihood of response in patients with previously untreated advanced renal-cell carcinoma. (Funded by Bristol Myers Squibb and others; CheckMate 9ER ClinicalTrials.gov number, NCT03141177.).
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