Pembrolizumab versus paclitaxel for previously treated, advanced gastric or gastro-oesophageal junction cancer (KEYNOTE-061): a randomised, open-label, controlled, phase 3 trial

被引:994
作者
Shitara, Kohei [1 ]
Ozguroglu, Mustafa [2 ]
Bang, Yung-Jue [3 ]
Di Bartolomeo, Maria [4 ]
Mandala, Mario [5 ]
Ryu, Min-Hee [6 ]
Fornaro, Lorenzo [7 ]
Olesinski, Tomasz [8 ]
Caglevic, Christian [9 ]
Chung, Hyun C. [10 ]
Muro, Kei [11 ]
Goekkurt, Eray [12 ,13 ]
Mansoor, Wasat [14 ]
McDermott, Raymond S. [15 ]
Shacham-Shmueli, Einat [16 ]
Chen, Xinqun [17 ]
Mayo, Carlos [17 ]
Kang, S. Peter [17 ]
Ohtsu, Atsushi [1 ]
Fuchs, Charles S. [18 ]
机构
[1] Natl Canc Ctr Hosp East, Kashiwa, Chiba 2770882, Japan
[2] Istanbul Univ, Cerrahpasa Sch Med, Istanbul, Turkey
[3] Seoul Natl Univ, Coll Med, Seoul, South Korea
[4] Fdn IRCCS Ist Nazl Tumori, Milan, Italy
[5] Papa Giovanni XXIII Hosp, Bergamo, Italy
[6] Univ Ulsan, Coll Med, Asan Med Ctr, Seoul, South Korea
[7] Azienda Osped Univ Pisana, Pisa, Italy
[8] Maria Sklodowska Curie Mem Canc Ctr, Warsaw, Poland
[9] Fdn Arturo Lopez Perez Clin Alemana Santiago, Santiago, Chile
[10] Yonsei Univ, Coll Med, Yonsei Canc Ctr, Seoul, South Korea
[11] Aichi Canc Ctr Hosp, Nagoya, Aichi, Japan
[12] HOPE, Hamburg, Germany
[13] Univ Canc Ctr Hamburg, Hamburg, Germany
[14] Christie Hosp NHS Fdn Trust, Manchester, Lancs, England
[15] Adelaide & Meath Hosp, Dublin, Ireland
[16] Sheba Med Ctr, Ramat Gan, Israel
[17] Merck & Co Inc, Kenilworth, NJ USA
[18] Smilow Canc Hosp, Yale Canc Ctr, New Haven, CT USA
关键词
SOLID TUMORS; DOUBLE-BLIND; NIVOLUMAB; MULTICENTER;
D O I
10.1016/S0140-6736(18)31257-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Patients with advanced gastric or gastro-oesophageal junction cancer that progresses on chemotherapy have poor outcomes. We compared pembrolizumab with paclitaxel in patients with advanced gastric or gastrooesophageal junction cancer that progressed on first-line chemotherapy with a platinum and fluoropyrimidine. Methods This randomised, open-label, phase 3 study was done at 148 medical centres in 30 countries. Eligible patients were randomised (1: 1) in blocks of four per stratum with an interactive voice-response and integrated web-response system to receive either pembrolizumab 200 mg every 3 weeks for up to 2 years or standard-dose paclitaxel. Primary endpoints were overall survival and progression-free survival in patients with a programmed cell death ligand 1 (PD-L1) combined positive score (CPS) of 1 or higher. Safety was assessed in all patients, irrespective of CPS. The significance threshold for overall survival was p=0.0135 (one-sided). This trial is registered at ClinicalTrials.gov, number NCT02370498. Findings Between June 4, 2015, and July 26, 2016, 592 patients were enrolled. Of the 395 patients who had a PD-L1 CPS of 1 or higher, 196 patients were assigned to receive pembrolizumab and 199 patients were assigned to receive paclitaxel. As of Oct 26, 2017, 326 patients in the population with CPS of 1 or higher had died (151 [77%] of 196 patients in the pembrolizumab group and 175 [88%] of 199 patients in the paclitaxel group). Median overall survival was 9.1 months (95% CI 6.2-10.7) with pembrolizumab and 8.3 months (7.6-9.0) with paclitaxel (hazard ratio [HR] 0.82, 95% CI 0.66-1.03; one-sided p=0.0421). Median progression-free survival was 1.5 months (95% CI 1.4-2.0) with pembrolizumab and 4.1 months (3.1-4.2) with paclitaxel (HR 1.27, 95% CI 1.03-1.57). In the total population, grade 3-5 treatment-related adverse events occurred in 42 (14%) of the 294 patients treated with pembrolizumab and 96 (35%) of the 276 patients treated with paclitaxel. Interpretation Pembrolizumab did not significantly improve overall survival compared with paclitaxel as second-line therapy for advanced gastric or gastro-oesophageal junction cancer with PD-L1 CPS of 1 or higher. Pembrolizumab had a better safety profile than paclitaxel. Additional trials of pembrolizumab in gastric and gastro-oesophageal cancer are ongoing. Copyright (c) 2018 Elsevier Ltd. All rights reserved.
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页码:123 / 133
页数:11
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