Adjuvant Osimertinib for Resected EGFR-Mutated Stage IB-IIIA Non-Small-Cell Lung Cancer: Updated Results From the Phase III Randomized ADAURA Trial

被引:225
作者
Herbst, Roy S. [1 ,2 ,12 ]
Wu, Yi-Long [3 ]
John, Thomas [4 ]
Grohe, Christian [5 ]
Majem, Margarita [6 ]
Wang, Jie [7 ]
Kato, Terufumi [8 ]
Goldman, Jonathan W. [9 ]
Laktionov, Konstantin [10 ]
Kim, Sang-We [11 ]
Yu, Chong-Jen
Vu, Huu Vinh
Lu, Shun
Lee, Kye Young
Mukhametshina, Guzel
Akewanlop, Charuwan
de Marinis, Filippo
Bonanno, Laura
Domine, Manuel
Shepherd, Frances A.
Urban, Damien
Huang, Xiangning
Bolanos, Ana
Stachowiak, Marta
Tsuboi, Masahiro
机构
[1] Yale Sch Med, Med Oncol, New Haven, CT USA
[2] Yale Canc Ctr, New Haven, CT USA
[3] Guangdong Prov Peoples Hosp & Guangdong Acad Med, Guangdong Lung Canc Inst, Guangzhou, Peoples R China
[4] Austin Hlth, Dept Med Oncol, Melbourne, Australia
[5] Klin Pneumol Evangel Lungenklin Berlin Buch, Berlin, Germany
[6] Hosp Santa Creu I St Pau, Dept Med Oncol, Barcelona, Spain
[7] Chinese Acad Med Sci, Canc Hosp, Beijing, Peoples R China
[8] Kanagawa Canc Ctr, Dept Thorac Oncol, Yokohama, Japan
[9] Univ Calif Los Angeles, David Geffen Sch Med, Los Angeles, CA USA
[10] Minist Hlth Russian Federat, Fed State Budgetary Inst, NNBlokhin Natl Med Res Ctr Oncol, Moscow, Russia
[11] Asan Med Ctr, Dept Oncol, Seoul, South Korea
[12] Yale Sch Med, Yale Comprehens Canc Ctr, 333 Cedar St,POB 208028, New Haven, CT 06520 USA
关键词
THERAPY;
D O I
10.1200/JCO.22.02186
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PURPOSE The phase III ADAURA (ClinicalTrials.gov identifier: NCT02511106) primary analysis demonstrated a clinically significant disease-free survival (DFS) benefit with adjuvant osimertinib versus placebo in EGFR-mutated stage IB-IIIA non-small-cell lung cancer (NSCLC) after complete tumor resection (DFS hazard ratio [HR], 0.20 [99.12% CI, 0.14 to 0.30]; P < .001). We report an updated exploratory analysis of final DFS data. METHODS Overall, 682 patients with stage IB-IIIA (American Joint Committee on Cancer/Union for International Cancer Control, seventh edition) EGFR-mutated (exon 19 deletion/L858R) NSCLC were randomly assigned 1:1 (stratified by stage, mutational status, and race) to receive osimertinib 80 mg once-daily or placebo for 3 years. The primary end point was DFS by investigator assessment in stage II-IIIA disease analyzed by stratified log-rank test; following early reporting of statistical significance in DFS, no further formal statistical testing was planned. Secondary end points included DFS in stage IB-IIIA, overall survival, and safety. Patterns of recurrence and CNS DFS were prespecified exploratory end points. RESULTS At data cutoff (April 11, 2022), in stage II-IIIA disease, median follow-up was 44.2 months (osimertinib) and 19.6 months (placebo); the DFS HR was 0.23 (95% CI, 0.18 to 0.30); 4-year DFS rate was 70% (osimertinib) and 29% (placebo). In the overall population, DFS HR was 0.27 (95% CI, 0.21 to 0.34); 4-year DFS rate was 73% (osimertinib) and 38% (placebo). Fewer patients treated with osimertinib had local/regional and distant recurrence versus placebo. CNS DFS HR in stage II-IIIA was 0.24 (95% CI, 0.14 to 0.42). The long-term safety profile of osimertinib was consistent with the primary analysis. CONCLUSION These updated data demonstrate prolonged DFS benefit over placebo, reduced risk of local and distant recurrence, improved CNS DFS, and a consistent safety profile, supporting the efficacy of adjuvant osimertinib in resected EGFR-mutated NSCLC. (c) 2023 by American Society of Clinical Oncology
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页码:1830 / +
页数:12
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