Four-Year Survival With Durvalumab After Chemoradiotherapy in Stage III NSCLC-an Update From the PACIFIC Trial.


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:
05 2021
Historique:
received: 09 10 2020
revised: 02 12 2020
accepted: 23 12 2020
pubmed: 22 1 2021
medline: 25 5 2021
entrez: 21 1 2021
Statut: ppublish

Résumé

In the Phase 3, placebo-controlled PACIFIC trial of patients with unresectable, stage III NSCLC without disease progression after concurrent chemoradiotherapy, consolidative durvalumab was associated with significant improvements in the primary end points of overall survival (OS) (hazard ratio [HR] = 0.68; 95% confidence interval [CI]: 0.53-0.87; p = 0.00251; data cutoff, March 22, 2018) and progression-free survival (PFS) (blinded independent central review; Response Evaluation Criteria in Solid Tumors version 1.1) (HR = 0.52; 95% CI: 0.42-65; p < 0.0001; February 13, 2017) with manageable safety. Here, we report updated analyses of OS and PFS, approximately 4 years after the last patient was randomized. Patients with WHO performance status of 0 or 1 (and any tumor programmed death-ligand 1 status) were randomized (2:1) to intravenous durvalumab (10 mg/kg) or placebo, administered every 2 weeks (≤12 months), stratified by age, sex, and smoking history. OS and PFS were analyzed using a stratified log-rank test in the intent-to-treat population. Medians and 4-year OS and PFS rates were estimated by the Kaplan-Meier method. Overall, 709 of 713 randomized patients received durvalumab (n/N=473/476) or placebo (n/N=236/237). As of March 20, 2020 (median follow-up = 34.2 months; range: 0.2-64.9), updated OS (HR = 0.71; 95% CI: 0.57-0.88) and PFS (HR = 0.55; 95% CI: 0.44-0.67) remained consistent with the primary analyses. The median OS for durvalumab was reached (47.5 mo; placebo, 29.1 months). Estimated 4-year OS rates were 49.6% versus 36.3% for durvalumab versus placebo, and 4-year PFS rates were 35.3% versus 19.5% respectively. These updated exploratory analyses demonstrate durable PFS and sustained OS benefit with durvalumab after chemoradiotherapy. An estimated 49.6% of patients randomized to durvalumab remain alive at 4 years (placebo, 36.3%), and 35.3% remain alive and progression-free (placebo, 19.5%).

Identifiants

pubmed: 33476803
pii: S1556-0864(21)00022-8
doi: 10.1016/j.jtho.2020.12.015
pii:
doi:

Substances chimiques

Antibodies, Monoclonal 0
durvalumab 28X28X9OKV

Banques de données

ClinicalTrials.gov
['NCT02125461']

Types de publication

Clinical Trial, Phase III Journal Article Randomized Controlled Trial Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

860-867

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States

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

Corinne Faivre-Finn (C)

The University of Manchester, Manchester, United Kingdom; The Christie NHS Foundation Trust, Manchester, United Kingdom. Electronic address: corinne.finn@nhs.net.

David Vicente (D)

Department of Medical Oncology, Hospital Universitario Virgen Macarena, Seville, Spain.

Takayasu Kurata (T)

Department of Internal Medicine, Kansai Medical University Hospital, Hirakata, Japan.

David Planchard (D)

Department of Medical Oncology, Thoracic Unit, Gustave Roussy, Villejuif, France.

Luis Paz-Ares (L)

CiberOnc, Universidad Complutense, Madrid, Spain; Centro Nacional De Investigaciones Oncologicas (CNIO), Hospital Universitario 12 de Octubre, Madrid, Spain.

Johan F Vansteenkiste (JF)

Department of Chronic Disease and Metabolism, University Hospitals KU Leuven, Leuven, Belgium.

David R Spigel (DR)

Sarah Cannon Research Institute/Tennessee Oncology, Nashville, Tennessee.

Marina C Garassino (MC)

Division of Medical Oncology, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Istituto Nazionale dei Tumori, Milan, Italy.

Martin Reck (M)

Lung Clinic Grosshansdorf, Airway Research Center North, German Center for Lung Research, Grosshansdorf, Germany.

Suresh Senan (S)

Department of Radiation Oncology, Amsterdam University Medical Centers, Vrije Universiteit Amsterdam, Cancer Center Amsterdam, Amsterdam, The Netherlands.

Jarushka Naidoo (J)

Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins University, Baltimore, Maryland; Bloomberg-Kimmel Institute for Cancer Immunotherapy at John Hopkins University, Baltimore, Maryland.

Andreas Rimner (A)

Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, New York.

Yi-Long Wu (YL)

Department of Pulmonary Oncology, Guangdong Lung Cancer Institute, Guangdong Provincial People's Hospital & Guangdong Academy of Medical Sciences, Guangzhou, People's Republic of China.

Jhanelle E Gray (JE)

Department of Thoracic Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.

Mustafa Özgüroğlu (M)

Division of Medical Oncology, Department of Internal Medicine, Cerrahpaşa School of Medicine, Istanbul University - Cerrahpaşa, Istanbul, Turkey.

Ki H Lee (KH)

Department of Internal Medicine, Chungbuk National University Hospital, Chungbuk National University College of Medicine, Cheongju, Korea.

Byoung C Cho (BC)

Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, Korea.

Terufumi Kato (T)

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

Maike de Wit (M)

Department of Hematology, Oncology, and Palliative Medicine, Vivantes Klinikum Neukölln, Berlin, Germany.

Michael Newton (M)

Department of Clinical Oncology, AstraZeneca, Gaithersburg, Maryland.

Lu Wang (L)

Department of Clinical Oncology, AstraZeneca, Gaithersburg, Maryland.

Piruntha Thiyagarajah (P)

Department of Clinical Oncology, AstraZeneca, Cambridge, United Kingdom.

Scott J Antonia (SJ)

Department of Thoracic Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.

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