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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.
Reck, Martin; Barlesi, Fabrice; Yang, James Chih-Hsin; Westeel, Virginie; Felip, Enriqueta; Özgüroglu, Mustafa; Dols, Manuel Cobo; Sullivan, Richard; Kowalski, Dariusz M; Andric, Zoran; Lee, Dae Ho; Sezer, Ahmet; Hu, Ping; Wang, XiaoZhe; von Heydebreck, Anja; Jacob, Natalia; Mehr, Keyvan Tadjalli; Park, Keunchil.
Afiliação
  • Reck M; LungenClinic Grosshansdorf, Airway Research Center North, German Center for Lung Research, Grosshansdorf, Germany. Electronic address: m.reck@lungenclinic.de.
  • Barlesi F; Université Paris Saclay, Faculté de Médecine, Kremlin Bicêtre, France; Medical Oncology department, Gustave Roussy, Villejuif, France; Present Address: Université Paris Saclay, Faculté de Médecine, Kremlin Bicêtre, France; Medical Oncology Department, Gustave Roussy, Villejuif, France.
  • Yang JC; National Taiwan University Hospital, Taipei, Taiwan.
  • Westeel V; Hôpital Jean Minjoz, Centre hospitalier universitaire de Besançon, UMR1098, Université de Franche, Comté, France.
  • Felip E; Hospital Universitari Vall d'Hebron, Barcelona, Spain.
  • Özgüroglu M; Department of Internal Medicine, Division of Medical Oncology, Cerrahpasa Medical Faculty, Istanbul University-Cerrahpasa, Istanbul, Turkey.
  • Dols MC; Medical Oncology Intercenter Unit, Regional and Virgen de la Victoria University Hospitals, IBIMA, Málaga, Spain; Present address: UGC Intercentros de Oncología Médica, Hospitales Universitarios Regional y Virgen de la Victoria, IBIMA, Málaga, Spain.
  • Sullivan R; Auckland City Hospital, Auckland, Australia.
  • Kowalski DM; Department of Lung Cancer and Thoracic Tumours, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
  • Andric Z; Clinical Center Bezanijska Kosa, Belgrade, Serbia.
  • Lee DH; Asan Medical Center, Seoul, South Korea.
  • Sezer A; Baskent University Adana Application and Research Center, Adana, Turkey.
  • Hu P; EMD Serono Research & Development Institute, Inc., Billerica, Massachusetts.
  • Wang X; EMD Serono Research & Development Institute, Inc., Billerica, Massachusetts.
  • von Heydebreck A; the healthcare business of Merck KGaA, Darmstadt, Germany.
  • Jacob N; the healthcare business of Merck KGaA, Darmstadt, Germany.
  • Mehr KT; the healthcare business of Merck KGaA, Darmstadt, Germany.
  • Park K; Division of Hematology-Oncology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea; Present Address: MD Anderson Cancer Center, Houston, Texas.
J Thorac Oncol ; 19(2): 297-313, 2024 02.
Article em En | MEDLINE | ID: mdl-37748693
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Anticorpos Monoclonais Humanizados / Neoplasias Pulmonares Tipo de estudo: Clinical_trials Limite: Adult / Humans Idioma: En Revista: J Thorac Oncol Ano de publicação: 2024 Tipo de documento: Article País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Anticorpos Monoclonais Humanizados / Neoplasias Pulmonares Tipo de estudo: Clinical_trials Limite: Adult / Humans Idioma: En Revista: J Thorac Oncol Ano de publicação: 2024 Tipo de documento: Article País de publicação: Estados Unidos