Osimertinib after Chemoradiotherapy in Stage III EGFR-Mutated NSCLC

被引:12
|
作者
Lu, Shun [1 ]
Kato, Terufumi [6 ]
Dong, Xiaorong [2 ]
Ahn, Myung-Ju [9 ]
Quang, Le-Van [10 ]
Soparattanapaisarn, Nopadol [12 ]
Inoue, Takako
Wang, Chih-Liang [16 ]
Huang, Meijuan [3 ,4 ]
Yang, James Chih-Hsin [17 ,18 ]
Cobo, Manuel [19 ]
Oezgueroglu, Mustafa [20 ]
Casarini, Ignacio [21 ]
Khiem, Dang-Van [11 ]
Sriuranpong, Virote [13 ,14 ]
Cronemberger, Eduardo [22 ]
Takahashi, Toshiaki [7 ,8 ]
Runglodvatana, Yotsawaj [15 ]
Chen, Ming [5 ]
Huang, Xiangning [23 ]
Grainger, Ellie [23 ]
Ghiorghiu, Dana [24 ]
van der Gronde, Toon [25 ]
Ramalingam, Suresh S. [26 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Chest Hosp, Sch Med, Dept Med Oncol, 241 Huai Hai Rd West, Shanghai, Peoples R China
[2] Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Canc Ctr, Wuhan, Peoples R China
[3] Sichuan Univ, West China Hosp, Canc Ctr, Div Thorac Tumor Multimodal Treatment, Chengdu, Peoples R China
[4] Sichuan Univ, West China Hosp, Canc Ctr, Dept Med Oncol, Chengdu, Peoples R China
[5] Univ Chinese Acad Sci, Chinese Acad Sci, Zhejiang Canc Hosp, Inst Basic Med & Canc,Canc Hosp,Dept Radiotherapy, Hangzhou, Peoples R China
[6] Kanagawa Canc Ctr, Dept Thorac Oncol, Yokohama, Japan
[7] Osaka Int Canc Inst, Dept Thorac Oncol, Osaka, Japan
[8] Shizuoka Canc Ctr, Div Thorac Oncol, Shizuoka, Japan
[9] Sungkyunkwan Univ, Samsung Med Ctr, Dept Hematol Oncol, Sch Med, Seoul, South Korea
[10] Hanoi Med Univ, Dept Oncol, Hanoi, Vietnam
[11] Vietnam Natl Lung Hosp, Dept Oncol, Hanoi, Vietnam
[12] Mahidol Univ, Siriraj Hosp, Fac Med, Bangkok, Thailand
[13] Chulalongkorn Univ, Fac Med, Div Med Oncol, Bangkok, Thailand
[14] King Chulalongkorn Mem Hosp, Bangkok, Thailand
[15] Navamindradhiraj Univ, Vajira Hosp, Fac Med, Bangkok, Thailand
[16] Med Coll Chang Gung Univ, Linkou Chang Gung Mem Hosp, Dept Thorac Med, Div Pulm Oncol & Intervent Bronchoscopy, Taoyuan, Taiwan
[17] Natl Taiwan Univ Hosp, Dept Oncol, Taipei, Taiwan
[18] Natl Taiwan Univ, Canc Ctr, Taipei, Taiwan
[19] Hosp Univ Reg & Virgen Victoria, Unidad Gest Clin Interctr Oncol Med, Inst Invest Biomed Malaga, Malaga, Spain
[20] Istanbul Univ Cerrahpasa, Cerrahpasa Fac Med, Dept Internal Med, Div Med Oncol,Clin Trial Unit, Istanbul, Turkiye
[21] Hosp Bernardo Houssay, Serv Oncol, Mar Del Plata, Buenos Aires, Argentina
[22] Ctr Reg Integrado Oncol, Ctr Pesquisa Clin, Fortaleza, Brazil
[23] AstraZeneca, Biometrics, Late Stage Dev, Oncol Res & Dev, Cambridge, England
[24] AstraZeneca, Late Stage Dev, Oncol Res & Dev, Baar, Switzerland
[25] AstraZeneca, Late Stage Dev, Oncol Res & Dev, New York, NY USA
[26] Emory Univ, Winship Canc Inst, Dept Hematol & Med Oncol, Sch Med, 1365 Clifton Rd NE,C-4014E, Atlanta, GA 30322 USA
关键词
CELL LUNG-CANCER; DURVALUMAB; CHEMORADIATION; DISEASE; TRIAL;
D O I
10.1056/NEJMoa2402614
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Osimertinib is a recommended treatment for advanced non-small-cell lung cancer (NSCLC) with an epidermal growth factor receptor (EGFR) mutation and as adjuvant treatment for resected EGFR-mutated NSCLC. EGFR-tyrosine kinase inhibitors have shown preliminary efficacy in unresectable stage III EGFR-mutated NSCLC. Methods In this phase 3, double-blind, placebo-controlled trial, we randomly assigned patients with unresectable EGFR-mutated stage III NSCLC without progression during or after chemoradiotherapy to receive osimertinib or placebo until disease progression occurred (as assessed by blinded independent central review) or the regimen was discontinued. The primary end point was progression-free survival as assessed by blinded independent central review. Results A total of 216 patients who had undergone chemoradiotherapy were randomly assigned to receive osimertinib (143 patients) or placebo (73 patients). Osimertinib resulted in a significant progression-free survival benefit as compared with placebo: the median progression-free survival was 39.1 months with osimertinib versus 5.6 months with placebo, with a hazard ratio for disease progression or death of 0.16 (95% confidence interval [CI], 0.10 to 0.24; P<0.001). The percentage of patients who were alive and progression free at 12 months was 74% (95% CI, 65 to 80) with osimertinib and 22% (95% CI, 13 to 32) with placebo. Interim overall survival data (maturity, 20%) showed 36-month overall survival among 84% of patients with osimertinib (95% CI, 75 to 89) and 74% with placebo (95% CI, 57 to 85), with a hazard ratio for death of 0.81 (95% CI, 0.42 to 1.56; P=0.53). The incidence of adverse events of grade 3 or higher was 35% in the osimertinib group and 12% in the placebo group; radiation pneumonitis (majority grade, 1 to 2) was reported in 48% and 38%, respectively. No new safety concerns emerged. Conclusions Treatment with osimertinib resulted in significantly longer progression-free survival than placebo in patients with unresectable stage III EGFR-mutated NSCLC. (Funded by AstraZeneca; LAURA ClinicalTrials.gov number, NCT03521154.)
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页数:13
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