Avelumab Versus Docetaxel in Patients With Platinum-Treated Advanced NSCLC: 2-Year Follow-Up From the JAVELIN Lung 200 Phase 3 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:
08 2021
Historique:
received: 18 12 2020
revised: 02 03 2021
accepted: 10 03 2021
pubmed: 13 4 2021
medline: 10 8 2021
entrez: 12 4 2021
Statut: ppublish

Résumé

In the JAVELIN Lung 200 trial, avelumab (anti-programmed death-ligand 1 [PD-L1] antibody) did not significantly prolong overall survival (OS) versus docetaxel in patients with platinum-treated PD-L1+ NSCLC. We report greater than 2-year follow-up data. Patients with stage IIIB or IV or recurrent NSCLC with disease progression after platinum-doublet chemotherapy were randomized 1:1 to avelumab 10 mg/kg every 2 weeks or docetaxel 75 mg/m Of 792 patients, 529 had PD-L1+ tumors (264 versus 265 in the avelumab versus docetaxel arms, respectively). As of March 4, 2019, median duration of follow-up for OS in the PD-L1+ population was 35.4 months in the avelumab arm and 34.7 months in the docetaxel arm; study treatment was ongoing in 25 (9.5%) versus 0 patients, respectively. In the PD-L1+ population, 2-year OS rates (95% confidence interval [CI]) with avelumab versus docetaxel were 29.9% (24.5%-35.5%) versus 20.5% (15.6%-25.8%); in greater than or equal to 50% PD-L1+ subgroups, 2-year OS rates were 36.4% (29.1%-43.7%) versus 17.7% (11.8%-24.7%) and in the greater than or equal to 80% subgroup were 40.2% (31.3%-49.0%) versus 20.3% (12.9%-28.8%), respectively. Median duration of response (investigator assessed) was 19.1 months (95% CI: 10.8-34.8) versus 5.7 months (95% CI: 4.1-8.3). Safety profiles for both arms were consistent with the primary analysis. Although the JAVELIN Lung 200 primary analysis (reported previously) revealed that avelumab did not significantly prolong OS versus docetaxel in patients with platinum-treated PD-L1+ NSCLC, posthoc analyses at 2 years of follow-up revealed that 2-year OS rates were doubled with avelumab in subgroups with higher PD-L1 expression (greater than or equal to 50% and greater than or equal to 80%).

Identifiants

pubmed: 33845211
pii: S1556-0864(21)01832-3
doi: 10.1016/j.jtho.2021.03.009
pii:
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
B7-H1 Antigen 0
Docetaxel 15H5577CQD
Platinum 49DFR088MY
avelumab KXG2PJ551I

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1369-1378

Informations de copyright

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

Auteurs

Keunchil Park (K)

Division of Hematology-Oncology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.

Mustafa Özgüroğlu (M)

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

Johan Vansteenkiste (J)

Department of Respiratory Oncology, University Hospital KU Leuven, Leuven, Belgium.

David Spigel (D)

Sarah Cannon Research Institute, Nashville, Tennessee.

James C H Yang (JCH)

Department of Medical Oncology, National Taiwan University Cancer Center, Taipei, Taiwan.

Hidenobu Ishii (H)

Department of Internal Medicine, Kurume University School of Medicine, Kurume, Japan.

Marina Garassino (M)

Thoracic Oncology Unit, Department of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Filippo de Marinis (F)

Thoracic Oncology Division, European Institute of Oncology, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Milan, Italy.

Aleksandra Szczesna (A)

Department of Lung Diseases, Regional Lung Disease Hospital, Otwock, Poland.

Andreas Polychronis (A)

Department of Medical Oncology, Mount Vernon Cancer Centre, Northwood, United Kingdom.

Ruchan Uslu (R)

Department of Medical Oncology, Ege University Hospital, Izmir, Turkey.

Maciej Krzakowski (M)

Centrum Onkologii-Instytut im. Marii Skłodowskiej-Curie w Warszawie, Warsaw, Poland.

Jong-Seok Lee (JS)

Department of Internal Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Republic of Korea.

Luana Calabrò (L)

Center for Immuno-Oncology, Medical Oncology and Immunotherapy, University Hospital of Siena, Siena, Italy.

Osvaldo Arén Frontera (O)

Instituto Nacional del Cáncer, Santiago, Chile.

Huiling Xiong (H)

EMD Serono Research & Development Institute Inc., Billerica, Massachusetts; an affiliate of Merck KGaA, Darmstadt, Germany.

Marcis Bajars (M)

EMD Serono Research & Development Institute Inc., Billerica, Massachusetts; an affiliate of Merck KGaA, Darmstadt, Germany.

Mary Ruisi (M)

EMD Serono Research & Development Institute Inc., Billerica, Massachusetts; an affiliate of Merck KGaA, Darmstadt, Germany.

Fabrice Barlesi (F)

CRCM, INSERM, CNRS, Aix Marseille University, Marseille, France(∗); Gustave Roussy Cancer Campus, Villejuif, France. Electronic address: Fabrice.BARLESI@gustaveroussy.fr.

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Classifications MeSH