Long-Term Overall Survival From KEYNOTE-021 Cohort G: Pemetrexed and Carboplatin With or Without Pembrolizumab as First-Line Therapy for Advanced Nonsquamous NSCLC

被引:115
作者
Awad, Mark M. [1 ]
Gadgeel, Shirish M. [2 ]
Borghaei, Hossein [3 ]
Patnaik, Amita [4 ]
Yang, James Chih-Hsin [5 ,6 ]
Powell, Steven F. [7 ]
Gentzler, Ryan D. [8 ]
Martins, Renato G. [9 ]
Stevenson, James P. [10 ]
Altan, Mehmet [11 ]
Jalal, Shadia I. [12 ]
Panwalkar, Amit [13 ]
Gubens, Matthew [14 ]
Sequist, Lecia V. [15 ]
Saraf, Sanatan [16 ]
Zhao, Bin [16 ]
Piperdi, Bilal [16 ]
Langer, Corey J. [17 ]
机构
[1] Dana Farber Canc Inst, Lowe Ctr Thorac Oncol, Med Oncol, 450 Brookline Ave,Dana 1240G, Boston, MA 02115 USA
[2] Wayne State Univ, Karmanos Canc Inst, Thorac Oncol, Detroit, MI USA
[3] Fox Chase Canc Ctr, Hematol & Oncol, 7701 Burholme Ave, Philadelphia, PA 19111 USA
[4] START Ctr Canc Care, Clin Res, San Antonio, TX USA
[5] Natl Taiwan Univ Hosp, Dept Oncol, Taipei, Taiwan
[6] Natl Taiwan Univ, Ctr Canc, Taipei, Taiwan
[7] Sanford Hlth, Oncol, Sioux Falls, SD USA
[8] Univ Virginia, Ctr Canc, Hematol Oncol, Charlottesville, VA 22908 USA
[9] Univ Washington, Dept Med, Seattle, WA USA
[10] Cleveland Clin, Taussig Canc Inst, Cleveland, OH 44106 USA
[11] Univ Texas MD Anderson Canc Ctr, Thorac Head & Neck Oncol, Houston, TX 77030 USA
[12] Indiana Univ Sch Med, Indianapolis, IN 46202 USA
[13] Sanford Roger Maris Canc Ctr, Hematol Oncol, Fargo, ND USA
[14] Univ Calif San Francisco, Med Oncol, San Francisco, CA 94143 USA
[15] Massachusetts Gen Hosp, Hematol Oncol, Boston, MA 02114 USA
[16] Merck & Co Inc, Kenilworth, NJ USA
[17] Univ Penn, Dept Med, Abramson Canc Ctr, Philadelphia, PA 19104 USA
关键词
Pembrolizumab; Chemotherapy; Advanced non-squamous non-small-cell lung cancer; Long-term survival; First-line therapy;
D O I
10.1016/j.jtho.2020.09.015
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: In cohort G of KEYNOTE-021 (NCT02039674), first-line pembrolizumab plus pemetrexed-carboplatin significantly improved the objective response rate and progression-free survival versus chemotherapy alone with manageable toxicity in advanced nonsquamous NSCLC. We report the long-term outcomes from this study. Methods: Patients with previously untreated advanced nonsquamous NSCLC without sensitizing EGFR or ALK alterations were randomly assigned 1:1 to receive open-label pemetrexed 500 mg/m(2) plus carboplatin at area under the concentration-time curve of 5 mg/mL/min (four cycles) with or without pembrolizumab 200 mg (up to 2 years), with optional pemetrexed maintenance, each administered every 3 weeks. Eligible patients could crossover from the chemotherapy arm to pembrolizumab monotherapy after progression. Responses were assessed per the Response Evaluation Criteria in Solid Tumors version 1.1. Results: After the median time of 49.4 months from randomization to data cutoff, objective response rate (58% versus 33%) and progression-free survival (median: 24.5 versus 9.9 mo; hazard ratio: 0.54; 95% confidence interval: 0.35.0.83) remained improved with pembrolizumab combination (n = 60) versus chemotherapy (n = 63), regardless of programmed death ligand 1 status. Median overall survival was 34.5 versus 21.1 months (hazard ratio: 0.71; 95% confidence interval: 0.45.1.12), despite a 70% crossover rate from chemotherapy alone to anti-programmed death (ligand) 1 therapy. Among the 12 patients who completed 2 years of pembrolizumab, 92% were alive at data cutoff; the estimated 3-year duration of response rate was 100%. Grade 3 to 5 treatment-related adverse events occurred in 39% of patients receiving pembrolizumab combination and 31% receiving chemotherapy. Conclusions: First-line pembrolizumab plus pemetrexed-carboplatin continued to show improved response and survival versus chemotherapy alone in advanced nonsquamous NSCLC, with durable clinical benefit in patients who completed 2 years of therapy. No new safety signals were observed with longer follow-up. (C) 2020 International Association for the Study of Lung Cancer. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:162 / 168
页数:7
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