Four-year survival with nivolumab in patients with previously treated advanced non-small-cell lung cancer: a pooled analysis

被引:265
作者
Antonia, Scott J. [1 ]
Borghaei, Hossein [2 ]
Ramalingam, Suresh S. [3 ]
Horn, Leora [4 ]
De Castro Carpeno, Javier [5 ]
Pluzanski, Adam [6 ]
Burgio, Marco A. [7 ]
Garassino, Marina [8 ]
Chow, Laura Q. M. [9 ]
Gettinger, Scott [10 ]
Crino, Lucio [7 ]
Planchard, David [11 ]
Butts, Charles [12 ]
Drilon, Alexander [13 ]
Wojcik-Tomaszewska, Joanna [14 ]
Otterson, Gregory A. [15 ]
Agrawal, Shruti [16 ]
Li, Ang [16 ]
Penrod, John R. [16 ]
Brahmer, Julie [17 ]
机构
[1] H Lee Moffitt Canc Ctr & Res Inst, Tampa, FL USA
[2] Fox Chase Canc Ctr, 7701 Burholme Ave, Philadelphia, PA 19111 USA
[3] Emory Univ, Winship Canc Inst, Atlanta, GA 30322 USA
[4] Vanderbilt Univ, Med Ctr, Nashville, TN USA
[5] Ctr Integral Oncol Clara Campal, Madrid, Spain
[6] Inst Marii Sklodowskiej Curie, Klin Nowotworow Pluca Klatki Piersiowej, Ctr Onkol, Warsaw, Poland
[7] Ist Sci Romagnolo Studio & Cura Tumori IRST IRCSS, Med Oncol Unit, Meldola, Italy
[8] Fdn IRCCS Ist Nazl Tumori, Dept Med Oncol, Milan, Italy
[9] Univ Washington, Dept Med, Div Med Oncol, Seattle, WA USA
[10] Yale Canc Ctr, New Haven, CT USA
[11] Inst Gustave Roussy, Dept Med Oncol, Thorac Grp, Villejuif, France
[12] CrossCanc Inst, Dept Oncol, Div Med Oncol, Edmonton, AB, Canada
[13] Mem Sloan Kettering Canc Ctr, 1275 York Ave, New York, NY 10021 USA
[14] Wojewodzkie Ctr Onkol, Gdansk, Poland
[15] Ohio State Univ, Columbus, OH 43210 USA
[16] Bristol Myers Squibb, Princeton, NJ USA
[17] Sidney Kimmel Comprehens Canc Ctr Johns Hopkins, Baltimore, MD USA
关键词
PHASE-III TRIALS; OPEN-LABEL; DOCETAXEL; SAFETY; ANTIBODY;
D O I
10.1016/S1470-2045(19)30407-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Phase 3 clinical data has shown higher proportions of patients with objective response, longer response duration, and longer overall survival with nivolumab versus docetaxel in patients with previously treated advanced non-small-cell lung cancer (NSCLC). We aimed to evaluate the long-term benefit of nivolumab and the effect of response and disease control on subsequent survival. Methods We pooled data from four clinical studies of nivolumab in patients with previously treated NSCLC (CheckMate 017, 057, 063, and 003) to evaluate survival outcomes. Trials of nivolumab in the second-line or later setting with at least 4 years follow-up were induded. Comparisons of nivolumab versus docetaxel included all randomised patients from the phase 3 ChedcMate 017 and 057 studies. We did landmark analyses by response status at 6 months to determine post-landmark survival outcomes. We excluded patients who did not have a radiographic tumour assessment at 6 months. Safety analyses included all patients who received at least one dose of nivolumab. Findings Across all four studies, 4-year overall survival with nivolumab was 14% (95% CI 11-17) for all patients (n=664), 19% (15-24) for those with at least 1% PD-Li expression, and 11% (7-16) for those with less than 1% PD-Ll expression. In CheckMate 017 and 057, 4-year overall survival was 14% (95% CI 11-18) in patients treated with nivolumab, compared with 5% (3-7) in patients treated with docetaxel. Survival subsequent to response at 6 months on nivoltimab or docetaxel was longer than after progressive disease at 6 months, with hazard ratios for overall survival of 0.18 (95% 0.12-0.27) for nivolumab and 0.43 (0- 29-0- 65) for docetaxel; for stable disease versus progressive disease, hazard ratios were 0.52 (0.37-0-71) for nivolumab and 0.80 (0- 61-1- 04) for docetaxel. Long-term data did not show any new safety signals. Interpretation Patients with advanced NSCLC treated with nivolumab achieved a greater duration of response compared with patients treated with docetaxel, which was associated with a long-term survival advantage. Copyright (C) 2019 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1395 / 1408
页数:14
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