First-Line Atezolizumab plus Chemotherapy in Extensive-Stage Small-Cell Lung Cancer

被引:2650
作者
Horn, L. [1 ]
Mansfield, A. S. [3 ]
Szczesna, A. [4 ]
Havel, L. [6 ]
Krzakowski, M. [5 ]
Hochmair, M. J. [7 ]
Huemer, F. [8 ]
Losonczy, G. [9 ]
Johnson, M. L. [2 ]
Nishio, M. [10 ]
Reck, M. [11 ]
Mok, T. [12 ]
Lam, S. [14 ]
Shames, D. S. [14 ]
Liu, J. [13 ]
Ding, B. [14 ]
Lopez-Chavez, A. [14 ]
Kabbinavar, F. [14 ]
Lin, W. [14 ]
Sandler, A. [14 ]
Liu, S. V. [15 ]
机构
[1] Vanderbilt Univ, Med Ctr, 2220 Pierce Ave,777 PRB, Nashville, TN 37232 USA
[2] Sarah Cannon Res Inst Tennessee Oncol, Nashville, TN USA
[3] Mayo Clin, Rochester, MN USA
[4] Mazowieckie Ctr Leczenia Chorob Pluc & Gruzlicy, Otwock, Poland
[5] Inst Marii Sklodowskiej Curie Warszawie, Ctr Onkol, Warsaw, Poland
[6] Pneumologicka Klin 1 LF UK, Thomayerova Nemocnice, Prague, Czech Republic
[7] Otto Wagner Spital, Dept Resp & Crit Care Med, Ludwig Boltzmann Inst COPD & Resp Epidemiol, Sozialmed Zentrum Baumgartner Hohe, Vienna, Austria
[8] Otto Wagner Spital, Dept Resp & Crit Care Med 2, Ludwig Boltzmann Inst COPD & Resp Epidemiol, Sozialmed Zentrum Baumgartner Hohe, Vienna, Austria
[9] Semmelweis Egyet AOK, Pulmonologiai Klin, Budapest, Hungary
[10] Japanese Fdn Canc Res, Canc Inst Hosp, Tokyo, Japan
[11] German Ctr Lung Res, LungenClin Grosshansdorf, Airway Res Ctr North, Grosshansdorf, Germany
[12] Chinese Univ Hong Kong, State Key Lab South China, Hong Kong, Hong Kong, Peoples R China
[13] Hoffmann La Roche, Shanghai, Peoples R China
[14] Genentech Inc, San Francisco, CA USA
[15] Georgetown Univ, Washington, DC USA
关键词
OPEN-LABEL; MULTICENTER; ASSOCIATION; IPILIMUMAB; EXPRESSION; DOCETAXEL; SURVIVAL; SAFETY; TRIAL;
D O I
10.1056/NEJMoa1809064
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Enhancing tumor-specific T-cell immunity by inhibiting programmed death ligand 1 (PD-L1)-programmed death 1 (PD-1) signaling has shown promise in the treatment of extensive-stage small-cell lung cancer. Combining checkpoint inhibition with cytotoxic chemotherapy may have a synergistic effect and improve efficacy. METHODS We conducted this double-blind, placebo-controlled, phase 3 trial to evaluate atezolizumab plus carboplatin and etoposide in patients with extensive-stage small-cell lung cancer who had not previously received treatment. Patients were randomly assigned in a 1:1 ratio to receive carboplatin and etoposide with either atezolizumab or placebo for four 21-day cycles (induction phase), followed by a maintenance phase during which they received either atezolizumab or placebo (according to the previous random assignment) until they had unacceptable toxic effects, disease progression according to Response Evaluation Criteria in Solid Tumors, version 1.1, or no additional clinical benefit. The two primary end points were investigator-assessed progression-free survival and overall survival in the intention-to-treat population. RESULTS A total of 201 patients were randomly assigned to the atezolizumab group, and 202 patients to the placebo group. At a median follow-up of 13.9 months, the median overall survival was 12.3 months in the atezolizumab group and 10.3 months in the placebo group (hazard ratio for death, 0.70; 95% confidence interval [CI], 0.54 to 0.91; P = 0.007). The median progression-free survival was 5.2 months and 4.3 months, respectively (hazard ratio for disease progression or death, 0.77; 95% CI, 0.62 to 0.96; P = 0.02). The safety profile of atezolizumab plus carboplatin and etoposide was consistent with the previously reported safety profile of the individual agents, with no new findings observed. CONCLUSIONS The addition of atezolizumab to chemotherapy in the first-line treatment of extensive-stage small-cell lung cancer resulted in significantly longer overall survival and progression-free survival than chemotherapy alone.
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收藏
页码:2220 / 2229
页数:10
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