| dc.contributor | Vall d'Hebron Barcelona Hospital Campus |
| dc.contributor.author | Westeel, Virginie |
| dc.contributor.author | ÖZGÜROGLU, MUSTAFA |
| dc.contributor.author | Reck, Martin |
| dc.contributor.author | Barlesi, Fabrice |
| dc.contributor.author | Yang, James Chih-Hsin |
| dc.contributor.author | FELIP, ENRIQUETA |
| dc.date.accessioned | 2024-02-20T09:40:46Z |
| dc.date.available | 2024-02-20T09:40:46Z |
| dc.date.issued | 2024-02 |
| dc.identifier.citation | Reck 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.issn | 1556-1380 |
| dc.identifier.uri | https://hdl.handle.net/11351/11083 |
| dc.description | Avelumab; Chemotherapy; Non–small cell lung cancer |
| dc.description.abstract | Introduction
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.iso | eng |
| dc.publisher | Elsevier |
| dc.relation.ispartofseries | Journal of Thoracic Oncology;19(2) |
| dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 International |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ |
| dc.source | Scientia |
| dc.subject | Pulmons - Càncer - Tractament |
| dc.subject | Anticossos monoclonals - Ús terapèutic |
| dc.subject | Medicaments antineoplàstics - Ús terapèutic |
| dc.subject.mesh | Carcinoma, Non-Small-Cell Lung |
| dc.subject.mesh | Antibodies, Monoclonal, Humanized |
| dc.subject.mesh | Antineoplastic Agents |
| dc.title | 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 |
| dc.type | info:eu-repo/semantics/article |
| dc.identifier.doi | 10.1016/j.jtho.2023.09.1445 |
| dc.subject.decs | carcinoma de pulmón de células no pequeñas |
| dc.subject.decs | anticuerpos monoclonales humanizados |
| dc.subject.decs | antineoplásicos |
| dc.relation.publishversion | https://doi.org/10.1016/j.jtho.2023.09.1445 |
| dc.type.version | info:eu-repo/semantics/publishedVersion |
| dc.audience | Professionals |
| dc.contributor.organismes | Institut 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.pmid | 37748693 |
| dc.rights.accessrights | info:eu-repo/semantics/openAccess |