Pembrolizumab plus Axitinib versus Sunitinib for Advanced Renal-Cell Carcinoma

被引:2554
作者
Rini, Brian I. [1 ]
Plimack, Elizabeth R. [2 ]
Stus, Viktor [3 ]
Gafanov, Rustem [7 ]
Hawkins, Robert [10 ]
Nosov, Dmitry [8 ]
Pouliot, Frederic [14 ,15 ]
Alekseev, Boris [9 ]
Soulieres, Denis [16 ]
Melichar, Bohuslav [17 ]
Vynnychenko, Ihor [5 ]
Kryzhanivska, Anna [6 ]
Bondarenko, Igor [4 ]
Azevedo, Sergio J. [18 ]
Borchiellini, Delphine [19 ]
Szczylik, Cezary [21 ]
Markus, Maurice [22 ]
McDermott, Raymond S. [23 ,24 ]
Bedke, Jens [25 ]
Tartas, Sophie [20 ]
Chang, Yen-Hwa [26 ]
Tamada, Satoshi [27 ]
Shou, Qiong [28 ]
Perini, Rodolfo F. [29 ]
Chen, Mei [29 ]
Atkins, Michael B. [30 ]
Powles, Thomas [11 ,12 ,13 ]
机构
[1] Cleveland Clin, Taussig Canc Inst, 9500 Euclid Ave,Desk CA60, Cleveland, OH 44195 USA
[2] Fox Chase Canc Ctr, 7701 Burholme Ave, Philadelphia, PA 19111 USA
[3] Minist Hlth Ukraine, Dnipropetrovsk Med Acad, Dnipro, Ukraine
[4] Dnipropetrovsk Med Acad, Dnipro, Ukraine
[5] Sumy State Univ, Sumy Reg Oncol Ctr, Sumy, Ukraine
[6] Ivano Frankivsk Natl Med Univ, Ivano Frankivsk, Ukraine
[7] Russian Sci Ctr Roentgen Radiol, Moscow, Russia
[8] Cent Clin Hosp, Outpatient Clin, Moscow, Russia
[9] Hertzen Moscow Canc Res Inst, Moscow, Russia
[10] Christie NHS Fdn Trust, Manchester, Lancs, England
[11] Barts Hlth NHS Trust, Barts Canc Inst, London, England
[12] Royal Free NHS Trust, Barts Canc Inst, London, England
[13] Queen Mary Univ London, London, England
[14] Ctr Hosp Univ CHU Quebec, Quebec City, PQ, Canada
[15] Univ Laval, Quebec City, PQ, Canada
[16] CHU Montreal, Montreal, PQ, Canada
[17] Palacky Univ, Med Sch & Teaching Hosp, Olomouc, Czech Republic
[18] Hosp Clin Porto Alegre, Porto Alegre, RS, Brazil
[19] Univ Cote Azur, Ctr Antoine Lacassagne, Nice, France
[20] Hop Univ Lyon, Lyon, France
[21] Mil Inst Med, Warsaw, Poland
[22] Rocky Mt Canc Ctr, Colorado Springs, CO USA
[23] Adelaide & Meath Hosp, Dublin, Ireland
[24] Univ Coll Dublin, Dublin, Ireland
[25] Eberhard Karls Univ Tubingen, Dept Urol, Tubingen, Germany
[26] Taipei Vet Gen Hosp, Taipei, Taiwan
[27] Osaka City Univ Hosp, Osaka, Japan
[28] MSD China, Beijing, Peoples R China
[29] Merck, Kenilworth, NJ USA
[30] Georgetown Lombardi Comprehens Canc Ctr, Washington, DC USA
关键词
BLIND PHASE-III; OPEN-LABEL; SURVIVAL; SORAFENIB; PAZOPANIB; THERAPY;
D O I
10.1056/NEJMoa1816714
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background The combination of pembrolizumab and axitinib showed antitumor activity in a phase 1b trial involving patients with previously untreated advanced renal-cell carcinoma. Whether pembrolizumab plus axitinib would result in better outcomes than sunitinib in such patients was unclear. Methods In an open-label, phase 3 trial, we randomly assigned 861 patients with previously untreated advanced clear-cell renal-cell carcinoma to receive pembrolizumab (200 mg) intravenously once every 3 weeks plus axitinib (5 mg) orally twice daily (432 patients) or sunitinib (50 mg) orally once daily for the first 4 weeks of each 6-week cycle (429 patients). The primary end points were overall survival and progression-free survival in the intention-to-treat population. The key secondary end point was the objective response rate. All reported results are from the protocol-specified first interim analysis. Results After a median follow-up of 12.8 months, the estimated percentage of patients who were alive at 12 months was 89.9% in the pembrolizumab-axitinib group and 78.3% in the sunitinib group (hazard ratio for death, 0.53; 95% confidence interval [CI], 0.38 to 0.74; P<0.0001). Median progression-free survival was 15.1 months in the pembrolizumab-axitinib group and 11.1 months in the sunitinib group (hazard ratio for disease progression or death, 0.69; 95% CI, 0.57 to 0.84; P<0.001). The objective response rate was 59.3% (95% CI, 54.5 to 63.9) in the pembrolizumab-axitinib group and 35.7% (95% CI, 31.1 to 40.4) in the sunitinib group (P<0.001). The benefit of pembrolizumab plus axitinib was observed across the International Metastatic Renal Cell Carcinoma Database Consortium risk groups (i.e., favorable, intermediate, and poor risk) and regardless of programmed death ligand 1 expression. Grade 3 or higher adverse events of any cause occurred in 75.8% of patients in the pembrolizumab-axitinib group and in 70.6% in the sunitinib group. Conclusions Among patients with previously untreated advanced renal-cell carcinoma, treatment with pembrolizumab plus axitinib resulted in significantly longer overall survival and progression-free survival, as well as a higher objective response rate, than treatment with sunitinib.
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收藏
页码:1116 / 1127
页数:12
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