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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorWesteel, Virginie
dc.contributor.authorÖZGÜROGLU, MUSTAFA
dc.contributor.authorReck, Martin
dc.contributor.authorBarlesi, Fabrice
dc.contributor.authorYang, James Chih-Hsin
dc.contributor.authorFELIP, ENRIQUETA
dc.date.accessioned2024-02-20T09:40:46Z
dc.date.available2024-02-20T09:40:46Z
dc.date.issued2024-02
dc.identifier.citationReck M, Barlesi F, Yang JCH, Westeel V, Felip E, Özgüroğlu M, et al. Avelumab Versus Platinum-Based Doublet Chemotherapy as First-Line Treatment for Patients With High-Expression Programmed Death-Ligand 1–Positive Metastatic NSCLC: Primary Analysis From the Phase 3 JAVELIN Lung 100 Trial. J Thorac Oncol. 2024 Feb;19(2):297–313.
dc.identifier.issn1556-1380
dc.identifier.urihttps://hdl.handle.net/11351/11083
dc.descriptionAvelumab; Chemotherapy; Non–small cell lung cancer
dc.description.abstractIntroduction We report the primary analysis from JAVELIN Lung 100, a phase 3 trial comparing avelumab (anti⁠–programmed death-ligand 1 [PD-L1]) versus platinum-based doublet chemotherapy as first-line treatment for PD-L1–positive (+) advanced NSCLC. Methods Adults with PD-L1+ (≥1% of tumor cells; PD-L1 immunohistochemistry 73-10 pharmDx), EGFR and ALK wild-type, previously untreated, stage IV NSCLC were randomized to avelumab 10 mg/kg every 2 weeks (Q2W), avelumab 10 mg/kg once weekly (QW) for 12 weeks and Q2W thereafter, or platinum-based doublet chemotherapy every 3 weeks. Primary end points were overall survival (OS) and progression-free survival (PFS) per independent review committee. The primary analysis population was patients with high-expression PD-L1+ tumors (≥80% of tumor cells). Results A total of 1214 patients were randomized to avelumab Q2W (n = 366), avelumab QW (n = 322), or chemotherapy (n = 526). In the primary analysis population, hazard ratios (HRs) for OS and PFS with avelumab Q2W (n = 151) versus chemotherapy (n = 216) were 0.85 (95% confidence interval [CI]: 0.67–1.09; one-sided p = 0.1032; median OS, 20.1 versus 14.9 mo) and 0.71 (95% CI: 0.54–0.93; one-sided p = 0.0070; median PFS, 8.4 versus 5.6 mo), respectively. With avelumab QW (n = 130) versus chemotherapy (n = 129), HRs were 0.79 (95% CI: 0.59–1.07; one-sided p = 0.0630; median OS, 19.3 versus 15.3 mo) and 0.72 (95% CI: 0.52–0.98; one-sided p = 0.0196; median PFS, 7.5 versus 5.6 mo), respectively. No new safety signals were observed. Conclusions Longer median OS and PFS were observed with avelumab versus platinum-based doublet chemotherapy in advanced NSCLC, but differences in OS and PFS were not statistically significant, and the trial did not meet its primary objective. ClinicalTrials.gov Identifier: NCT02576574.
dc.language.isoeng
dc.publisherElsevier
dc.relation.ispartofseriesJournal of Thoracic Oncology;19(2)
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceScientia
dc.subjectPulmons - Càncer - Tractament
dc.subjectAnticossos monoclonals - Ús terapèutic
dc.subjectMedicaments antineoplàstics - Ús terapèutic
dc.subject.meshCarcinoma, Non-Small-Cell Lung
dc.subject.meshAntibodies, Monoclonal, Humanized
dc.subject.meshAntineoplastic Agents
dc.titleAvelumab Versus Platinum-Based Doublet Chemotherapy as First-Line Treatment for Patients With High-Expression Programmed Death-Ligand 1–Positive Metastatic NSCLC: Primary Analysis From the Phase 3 JAVELIN Lung 100 Trial
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/j.jtho.2023.09.1445
dc.subject.decscarcinoma de pulmón de células no pequeñas
dc.subject.decsanticuerpos monoclonales humanizados
dc.subject.decsantineoplásicos
dc.relation.publishversionhttps://doi.org/10.1016/j.jtho.2023.09.1445
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Reck M] LungenClinic Grosshansdorf, Airway Research Center North, German Center for Lung Research, Grosshansdorf, Germany. [Barlesi F] Université Paris Saclay, Faculté de Médecine, Kremlin Bicêtre, France. Medical Oncology department, Gustave Roussy, Villejuif, France. Université Paris Saclay, Faculté de Médecine, Kremlin Bicêtre, France; Medical Oncology Department, Gustave Roussy, Villejuif, France. [Yang JCS] National Taiwan University Hospital, Taipei, Taiwan. [Westeel V] Hôpital Jean Minjoz, Centre hospitalier universitaire de Besançon, UMR1098, Université de Franche, Comté, France. [Felip E] Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Özgüroğlu M] Department of Internal Medicine, Division of Medical Oncology, Cerrahpaşa Medical Faculty, Istanbul University-Cerrahpaşa, Istanbul, Turkey
dc.identifier.pmid37748693
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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