From Memorial Sloan Kettering Cancer Center (R.J.M.) and Pfizer (S.H.), New York; Private Medical Institution Euromedservice (K.P.) and Nonstate Health Institution Road Clinical Hospital-Russian Railways (A.V.), St. Petersburg, and the Moscow Scientific Research Oncology Institute, Moscow (B.A.) - all in Russia; the Netherlands Cancer Institute, Amsterdam (J.H.); the Cleveland Clinic, Cleveland (B.R.); Institut Gustave Roussy, Villejuif (L.A.), and Centre Léon Bérard, University of Lyon, Lyon (S.N.) - both in France; the University of Texas M.D. Anderson Cancer Center, Houston (M.T.C.); University of Glasgow, Beatson West of Scotland Cancer Centre, Glasgow (B.V.), and Royal Marsden NHS Foundation Trust, London (J.L.) - both in the United Kingdom; British Columbia Cancer Agency, Vancouver (C.K.), and Lady Davis Institute and Jewish General Hospital, McGill University, Montreal (W.H.M.) - both in Canada; Osaka University Hospital, Osaka, Japan (M.U.); University of Ulsan College of Medicine, Asan Medical Center, Seoul, South Korea (J.L.L.); Macquarie University, Sydney (H.G.); Department of Medicine I, Clinical Division of Oncology and Comprehensive Cancer Center, Medical University of Vienna, Vienna (M.S.); Georgetown Lombardi Comprehensive Cancer Center, Washington, DC (M.B.A.); Department of Urology, University of Tübingen, Tübingen, Germany (J.B.); Pfizer, Cambridge (J.W., A.C.), and the Lank Center for Genitourinary Oncology at Dana-Farber Cancer Institute, and Brigham and Women's Hospital, Boston (T.K.C.) - both in Massachusetts; Pfizer (M.M., A.P.) and Pfizer Italia (C.F.), Milan; Pfizer, San Diego, CA (P.B.R.); and Pfizer, Groton, CT (B.H.).
N Engl J Med. 2019 Mar 21;380(12):1103-1115. doi: 10.1056/NEJMoa1816047. Epub 2019 Feb 16.
In a single-group, phase 1b trial, avelumab plus axitinib resulted in objective responses in patients with advanced renal-cell carcinoma. This phase 3 trial involving previously untreated patients with advanced renal-cell carcinoma compared avelumab plus axitinib with the standard-of-care sunitinib.
We randomly assigned patients in a 1:1 ratio to receive avelumab (10 mg per kilogram of body weight) intravenously every 2 weeks plus axitinib (5 mg) orally twice daily or sunitinib (50 mg) orally once daily for 4 weeks (6-week cycle). The two independent primary end points were progression-free survival and overall survival among patients with programmed death ligand 1 (PD-L1)-positive tumors. A key secondary end point was progression-free survival in the overall population; other end points included objective response and safety.
A total of 886 patients were assigned to receive avelumab plus axitinib (442 patients) or sunitinib (444 patients). Among the 560 patients with PD-L1-positive tumors (63.2%), the median progression-free survival was 13.8 months with avelumab plus axitinib, as compared with 7.2 months with sunitinib (hazard ratio for disease progression or death, 0.61; 95% confidence interval [CI], 0.47 to 0.79; P<0.001); in the overall population, the median progression-free survival was 13.8 months, as compared with 8.4 months (hazard ratio, 0.69; 95% CI, 0.56 to 0.84; P<0.001). Among the patients with PD-L1-positive tumors, the objective response rate was 55.2% with avelumab plus axitinib and 25.5% with sunitinib; at a median follow-up for overall survival of 11.6 months and 10.7 months in the two groups, 37 patients and 44 patients had died, respectively. Adverse events during treatment occurred in 99.5% of patients in the avelumab-plus-axitinib group and in 99.3% of patients in the sunitinib group; these events were grade 3 or higher in 71.2% and 71.5% of the patients in the respective groups.
Progression-free survival was significantly longer with avelumab plus axitinib than with sunitinib among patients who received these agents as first-line treatment for advanced renal-cell carcinoma. (Funded by Pfizer and Merck [Darmstadt, Germany]; JAVELIN Renal 101 ClinicalTrials.gov number, NCT02684006.).
在一项单组、1b 期试验中,avelumab 联合 axitinib 可使晚期肾细胞癌患者产生客观缓解。这项涉及未经治疗的晚期肾细胞癌患者的 3 期试验比较了avelumab 联合 axitinib 与标准治疗药物舒尼替尼。
我们以 1:1 的比例随机分配患者,接受avelumab(每公斤体重 10 毫克)每 2 周静脉注射一次,联合 axitinib(每天两次 5 毫克)口服,或舒尼替尼(每天一次 50 毫克)口服,每 4 周(6 周周期)一次。两个独立的主要终点是 PD-L1 阳性肿瘤患者的无进展生存期和总生存期。一个关键的次要终点是总体人群的无进展生存期;其他终点包括客观缓解率和安全性。
共有 886 名患者被分配接受avelumab 联合 axitinib(442 名)或舒尼替尼(444 名)治疗。在 560 名 PD-L1 阳性肿瘤患者(63.2%)中,avelumab 联合 axitinib 的中位无进展生存期为 13.8 个月,而舒尼替尼为 7.2 个月(疾病进展或死亡的风险比,0.61;95%置信区间[CI],0.47 至 0.79;P<0.001);在总体人群中,中位无进展生存期为 13.8 个月,而舒尼替尼为 8.4 个月(风险比,0.69;95%CI,0.56 至 0.84;P<0.001)。在 PD-L1 阳性肿瘤患者中,avelumab 联合 axitinib 的客观缓解率为 55.2%,舒尼替尼为 25.5%;在两组中位随访 11.6 个月和 10.7 个月时,分别有 37 名和 44 名患者死亡。avelumab 联合 axitinib 组和舒尼替尼组治疗期间发生的不良事件分别为 99.5%和 99.3%的患者;在两组中,分别有 71.2%和 71.5%的患者出现 3 级或以上的不良事件。
在接受avelumab 联合 axitinib 或舒尼替尼作为晚期肾细胞癌一线治疗的患者中,avelumab 联合 axitinib 可显著延长无进展生存期。(由辉瑞公司和默克公司[德国达姆施塔特]资助;JAVELIN Renal 101 临床试验.gov 编号,NCT02684006)。