Avelumab Versus Docetaxel in Patients With Platinum-Treated Advanced NSCLC: 2-Year Follow-Up From the JAVELIN Lung 200 Phase 3 Trial
Year: 2021
Type: article
Abstract: INTRODUCTION: 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. METHODS: every 3 weeks. The primary end point was OS in patients with PD-L1+ tumors (greater than or equal to 1% tumor cell expression; IHC 73-10 pharmDx assay). RESULTS: 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. CONCLUSIONS: 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%).
Source: Journal of Thoracic Oncology
Authors: Keunchil Park, Mustafa Özgüroğlu, Johan Vansteenkiste, David Spigel, James C.H. Yang, Hidenobu Ishii, Marina Garassino, Filippo de Marinis, Aleksandra Szczesna, Andreas Polychronis, Ruchan Uslu, Maciej Krzakowski, Jong-Seok Lee, Luana Calabrò, Osvaldo Arén Frontera, Huiling Xiong, Marcis Bajars, Mary Ruisi, Fabrice Barlesi
Institutions: Samsung Medical Center, Sungkyunkwan University, Istanbul University-Cerrahpaşa, Istanbul University, Universitair Ziekenhuis Leuven, KU Leuven, Sarah Cannon, National Taiwan University, Kurume University, Fondazione IRCCS Istituto Nazionale dei Tumori, European Institute of Oncology, Mount Vernon Cancer Centre, Ege Üniversitesi Tıp Fakültesi Hastanesi, The Maria Sklodowska-Curie National Research Institute of Oncology, Institut de Recherche Pierre Fabre (France), Seoul National University, Seoul National University Bundang Hospital, University of Siena, Azienda Ospedaliera Universitaria Senese, Instituto Nacional del Cáncer, Merck KGaA, Darmstadt (Germany), EMD Serono, Inc. (United States), Merck Healthcare KGaA, Darmstadt (Germany), Centre National de la Recherche Scientifique, Inserm, Aix-Marseille Université, Institut Gustave Roussy, Centre de Recherche en Cancérologie de Marseille
Language: English
Subfield: Oncology
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
Estimated APC paid: $2,800
Funders: Amgen, Bristol-Myers Squibb, Eli Lilly and Company, Pfizer, Astellas Pharma US, AstraZeneca, Bayer, GlaxoSmithKline, Merck, Novartis, Roche, Sanofi, American Society of Clinical Oncology, Celgene, AbbVie, Array BioPharma, Boehringer Ingelheim, Takeda Pharmaceutical Company, Handok, Merck KGaA, Aeglea BioTherapeutics, Les Laboratories Pierre Fabre, Clovis Oncology, Daiichi-Sankyo, Eisai, MedImmune, Ipsen, Genentech, EMD Serono, Merck Sharp and Dohme, Chugai Pharmaceutical, Takeda Oncology
OpenAlex ID: W3155244800
