Postoperative Chemotherapy Use and Outcomes From ADAURA: Osimertinib as Adjuvant Therapy for Resected EGFR-Mutated NSCLC.


Journal

Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer
ISSN: 1556-1380
Titre abrégé: J Thorac Oncol
Pays: United States
ID NLM: 101274235

Informations de publication

Date de publication:
03 2022
Historique:
received: 28 09 2021
accepted: 14 10 2021
pubmed: 7 11 2021
medline: 30 4 2022
entrez: 6 11 2021
Statut: ppublish

Résumé

Adjuvant chemotherapy is recommended in patients with resected stages II to IIIA (and select IB) NSCLC; however, recurrence rates are high. In the phase 3 ADAURA study (NCT02511106), osimertinib was found to have a clinically meaningful improvement in disease-free survival (DFS) in patients with resected stages IB to IIIA EGFR-mutated (EGFRm) NSCLC. Here, we report prespecified and exploratory analyses of adjuvant chemotherapy use and outcomes from ADAURA. Patients with resected stages IB to IIIA EGFRm NSCLC were randomized 1:1 to receive osimertinib or placebo for 3 years. Adjuvant chemotherapy before randomization was not mandatory, per physician and patient choice. DFS in the overall population (IB-IIIA), with and without adjuvant chemotherapy, was a prespecified analysis. Exploratory analyses included the following: adjuvant chemotherapy use by patient age, disease stage, and geographic location; DFS by adjuvant chemotherapy use and disease stage. Overall, 410 of 682 patients (60%) received adjuvant chemotherapy (osimertinib, n = 203; placebo, n = 207) for a median duration of 4.0 cycles. Adjuvant chemotherapy use was more frequent in patients: aged less than 70 years (338 of 509; 66%) versus more than or equal to 70 years (72 of 173; 42%); with stages II to IIIA (352 of 466; 76%) versus stage IB (57 of 216; 26%); and enrolled in Asia (268 of 414; 65%) versus outside of Asia (142 of 268; 53%). A DFS benefit favoring osimertinib versus placebo was observed in patients with (DFS hazard ratio = 0.16, 95% confidence interval: 0.10-0.26) and without adjuvant chemotherapy (hazard ratio = 0.23, 95% confidence interval: 0.13-0.40), regardless of disease stage. These findings support adjuvant osimertinib as an effective treatment for patients with stages IB to IIIA EGFRm NSCLC after resection, with or without previous adjuvant chemotherapy.

Identifiants

pubmed: 34740861
pii: S1556-0864(21)03285-8
doi: 10.1016/j.jtho.2021.10.014
pii:
doi:

Substances chimiques

Acrylamides 0
Aniline Compounds 0
osimertinib 3C06JJ0Z2O
EGFR protein, human EC 2.7.10.1
ErbB Receptors EC 2.7.10.1

Banques de données

ClinicalTrials.gov
['NCT02511106']

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

423-433

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2021 International Association for the Study of Lung Cancer. Published by Elsevier Inc. All rights reserved.

Auteurs

Yi-Long Wu (YL)

Guangdong Lung Cancer Institute, Guangdong Provincial People's Hospital and Guangdong Academy of Medical Sciences, Guangzhou, People's Republic of China. Electronic address: syylwu@live.cn.

Thomas John (T)

Department of Medical Oncology, Austin Health, Melbourne, Australia.

Christian Grohe (C)

Department of Respiratory Diseases, Evangelische Lungenklinik, Berlin, Germany.

Margarita Majem (M)

Department of Medical Oncology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

Jonathan W Goldman (JW)

David Geffen School of Medicine at University of California, Los Angeles, California.

Sang-We Kim (SW)

Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.

Terufumi Kato (T)

Department of Thoracic Oncology, Kanagawa Cancer Center, Yokohama, Japan.

Konstantin Laktionov (K)

Federal State Budgetary Institution N.N. Blokhin National Medical Research Center of Oncology of the Ministry of Health of the Russian Federation (N.N. Blokhin NMRCO), Moscow, Russia.

Huu Vinh Vu (HV)

Department of Thoracic Surgery, Choray Hospital, Ho Chi Minh City, Vietnam.

Zhijie Wang (Z)

State Key Laboratory of Molecular Oncology, Department of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, People's Republic of China.

Shun Lu (S)

Lung Cancer Center, Shanghai Chest Hospital, Shanghai Jiao Tong University, Shanghai, People's Republic of China.

Kye Young Lee (KY)

Precision Medicine Lung Cancer Center, Konkuk University Medical Center, Seoul, South Korea.

Charuwan Akewanlop (C)

Division of Medical Oncology, Faculty of Medicine, Siriraj Hospital, Bangkok, Thailand.

Chong-Jen Yu (CJ)

Department of Internal Medicine, National Taiwan University Hospital Hsinchu Branch and National Taiwan University College of Medicine, Taipei, Taiwan.

Filippo de Marinis (F)

Thoracic Oncology Division, European Institute of Oncology (IEO), IRCCS, Milan, Italy.

Laura Bonanno (L)

Medical Oncology 2, Istituto Oncologico Veneto IOV IRCCS, Padova, Italy.

Manuel Domine (M)

Oncology Department, Instituto de Investigación Sanitaria-Fundación Jiménez Díaz, Madrid, Spain.

Frances A Shepherd (FA)

Department of Medical Oncology and Hematology, University Health Network, Princess Margaret Cancer Centre and the University of Toronto, Toronto, Ontario, Canada.

Lingmin Zeng (L)

Late Oncology Statistics, AstraZeneca, Gaithersburg, Maryland.

Ajlan Atasoy (A)

Late Oncology Research & Development, AstraZeneca, Cambridge, United Kingdom.

Roy S Herbst (RS)

Medical Oncology, Yale School of Medicine and Yale Cancer Center, New Haven, Connecticut.

Masahiro Tsuboi (M)

Department of Thoracic Surgery and Oncology, National Cancer Center Hospital East, Kashiwa, Japan.

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Classifications MeSH