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Adjuvant Osimertinib for Resected EGFR-Mutated Stage IB-IIIA Non-Small-Cell Lung Cancer: Updated Results From the Phase III Randomized ADAURA Trial.
Herbst, Roy S; Wu, Yi-Long; John, Thomas; Grohe, Christian; Majem, Margarita; Wang, Jie; Kato, Terufumi; Goldman, Jonathan W; Laktionov, Konstantin; Kim, Sang-We; 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.
Afiliação
  • Herbst RS; Medical Oncology, Yale School of Medicine and Yale Cancer Center, New Haven, CT.
  • Wu YL; Guangdong Lung Cancer Institute, Guangdong Provincial People's Hospital and Guangdong Academy of Medical Sciences, Guangzhou, China.
  • John T; Department of Medical Oncology, Austin Health, Melbourne, Australia.
  • Grohe C; Klinik für Pneumologie-Evangelische Lungenklinik Berlin Buch, Berlin, Germany.
  • Majem M; Department of Medical Oncology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
  • Wang J; Cancer Hospital Chinese Academy of Medical Sciences, Beijing, China.
  • Kato T; Department of Thoracic Oncology, Kanagawa Cancer Center, Yokohama, Japan.
  • Goldman JW; David Geffen School of Medicine at University of California Los Angeles, Los Angeles, CA.
  • Laktionov K; Federal State Budgetary Institution "N.N.Blokhin National Medical Research Center of Oncology" of the Ministry of Health of the Russian Federation, Moscow, Russia.
  • Kim SW; Department of Oncology, Asan Medical Center, Seoul, South Korea.
  • Yu CJ; Department of Internal Medicine, National Taiwan University College of Medicine, Taipei, Taiwan.
  • Vu HV; National Taiwan University Hospital Hsin-Chu Branch, Zhubei City, Hsin-Chu County, Taiwan.
  • Lu S; Department Thoracic Surgery, Cho Ray Hospital, Hochiminh City, Vietnam.
  • Lee KY; Department of Internal Medicine, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan.
  • Mukhametshina G; Precision Medicine Lung Cancer Center, Konkuk University Medical Center, Seoul, South Korea.
  • Akewanlop C; Republican Clinical Oncology Center, Kazan, Republic of Tatarstan, Russia.
  • de Marinis F; Division of Medical Oncology, Faculty of Medicine, Siriraj Hospital, Bangkok, Thailand.
  • Bonanno L; Thoracic Oncology Division, European Institute of Oncology (IEO), IRCCS, Milan, Italy.
  • Domine M; Medical Oncology 2, Istituto Oncologico Veneto IOV IRCCS, Padova, Italy.
  • Shepherd FA; Department of Oncology, Hospital Universitario Fundación Jiménez Díaz (IIS-FJD), Madrid, Spain.
  • Urban D; Department of Medical Oncology and Hematology, University Health Network, Princess Margaret Cancer Center, Toronto, Canada.
  • Huang X; Department of Oncology, Sheba Medical Center, Tel Hashomer, Israel.
  • Bolanos A; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Stachowiak M; Oncology Biometrics, AstraZeneca, Cambridge, United Kingdom.
  • Tsuboi M; Oncology Research and Development, AstraZeneca, Toronto, Ontario, Canada.
J Clin Oncol ; 41(10): 1830-1840, 2023 04 01.
Article em En | MEDLINE | ID: mdl-36720083
ABSTRACT

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 11 (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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares / Antineoplásicos Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans Idioma: En Revista: J Clin Oncol Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares / Antineoplásicos Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans Idioma: En Revista: J Clin Oncol Ano de publicação: 2023 Tipo de documento: Article
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