First-Line Selpercatinib or Chemotherapy and Pembrolizumab in RET Fusion-Positive NSCLC

被引:96
作者
Zhou, Caicun [1 ]
Solomon, Benjamin [5 ]
Loong, Herbert H. [3 ]
Park, Keunchil [6 ]
Perol, Maurice [7 ]
Arriola, Edurne [8 ]
Novello, Silvia [9 ]
Han, Baohui [2 ]
Zhou, Jianying [4 ]
Ardizzoni, Andrea [10 ]
Mak, M. Perez [11 ,12 ]
Santini, Fernando C. [13 ]
Elamin, Yasir Y. [14 ]
Drilon, Alexander [15 ,16 ]
Wolf, Juergen [17 ]
Payakachat, Nalin [19 ]
Uh, Minji K. [19 ]
Rajakumar, Deborah [19 ]
Han, Hongmei [18 ]
Puri, Tarun [19 ]
Soldatenkova, Victoria [19 ]
Lin, A. Bence [19 ]
Lin, Boris K. [19 ]
Goto, Koichi [20 ]
机构
[1] Tongji Univ, Shanghai Pulm Hosp, Sch Med, Shanghai, Peoples R China
[2] Shanghai Jiao Tong Univ, Shanghai Chest Hosp, Sch Med, Dept Resp & Crit Care Med, Shanghai, Peoples R China
[3] Chinese Univ Hong Kong, Hong Kong, Peoples R China
[4] Zhejiang Univ, Affiliated Hosp 1, Sch Med, Hangzhou, Peoples R China
[5] Peter MacCallum Canc Inst, Melbourne, Vic, Australia
[6] Sungkyunkwan Univ, Samsung Med Ctr, Sch Med, Seoul, South Korea
[7] Ctr Leon Berard, Lyon, France
[8] Hosp Del Mar, Barcelona, Spain
[9] Univ Turin, Azienda Osped Univ San Luigi Orbassano, Dept Oncol, Turin, Italy
[10] IRCCS Azienda Osped Univ Bologna, Bologna, Italy
[11] Univ Sao Paulo, Inst Canc Estado Sao Paulo, Med Sch, Sao Paulo, Brazil
[12] Inst Ensino & Pesquisa, Sao Paulo, Brazil
[13] Hosp Sirio Libanes, Oncol Ctr, Sao Paulo, Brazil
[14] Univ Texas MD Anderson Canc Ctr, Houston, TX USA
[15] Mem Sloan Kettering Canc Ctr, New York, NY USA
[16] Weill Cornell Med Coll, New York, NY USA
[17] Univ Hosp Cologne, Ctr Integrated Oncol, Cologne, Germany
[18] Loxo Lilly, Indianapolis, IN USA
[19] Eli Lilly, Indianapolis, IN USA
[20] Natl Canc Ctr Hosp East, Kashiwa, Japan
关键词
CELL LUNG-CANCER; SYMPTOM BURDEN; SOLID TUMORS; EFFICACY; LIBRETTO-001; PLATINUM; OUTCOMES;
D O I
10.1056/NEJMoa2309457
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BackgroundSelpercatinib, a highly selective potent and brain-penetrant RET inhibitor, was shown to have efficacy in patients with advanced RET fusion-positive non-small-cell lung cancer (NSCLC) in a nonrandomized phase 1-2 study.MethodsIn a randomized phase 3 trial, we evaluated the efficacy and safety of first-line selpercatinib as compared with control treatment that consisted of platinum-based chemotherapy with or without pembrolizumab at the investigator's discretion. The primary end point was progression-free survival assessed by blinded independent central review in both the intention-to-treat-pembrolizumab population (i.e., patients whose physicians had planned to treat them with pembrolizumab in the event that they were assigned to the control group) and the overall intention-to-treat population. Crossover from the control group to the selpercatinib group was allowed if disease progression as assessed by blinded independent central review occurred during receipt of control treatment.ResultsIn total, 212 patients underwent randomization in the intention-to-treat-pembrolizumab population. At the time of the preplanned interim efficacy analysis, median progression-free survival was 24.8 months (95% confidence interval [CI], 16.9 to not estimable) with selpercatinib and 11.2 months (95% CI, 8.8 to 16.8) with control treatment (hazard ratio for progression or death, 0.46; 95% CI, 0.31 to 0.70; P<0.001). The percentage of patients with an objective response was 84% (95% CI, 76 to 90) with selpercatinib and 65% (95% CI, 54 to 75) with control treatment. The cause-specific hazard ratio for the time to progression affecting the central nervous system was 0.28 (95% CI, 0.12 to 0.68). Efficacy results in the overall intention-to-treat population (261 patients) were similar to those in the intention-to-treat-pembrolizumab population. The adverse events that occurred with selpercatinib and control treatment were consistent with those previously reported.ConclusionsTreatment with selpercatinib led to significantly longer progression-free survival than platinum-based chemotherapy with or without pembrolizumab among patients with advanced RET fusion-positive NSCLC. (Funded by Eli Lilly and others; ClinicalTrials.gov number, NCT04194944.)
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页码:1839 / 1850
页数:12
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