LEAP-008: Lenvatinib Plus Pembrolizumab for Metastatic NSCLC That Has Progressed After an Anti–Programmed Cell Death Protein 1 or Anti–Programmed Cell Death Ligand 1 Plus Platinum Chemotherapy

Lenvatinib plus pembrolizumab did not improve efficacy versus docetaxel in participants with stage IV NSCLC that progressed on anti‒programmed cell death protein 1 or anti-programmed cell death ligand 1 therapy and platinum-containing chemotherapy. There were no unexpected safety signals. More effective therapies are needed for this patient population.

Authors

Institutions

Publication Details

Journal
Journal of Thoracic Oncology
Published
2025-06-03
DOI
https://doi.org/10.1016/j.jtho.2025.05.020
Citations
15
Primary Topic
Cancer Immunotherapy and Biomarkers
Type
article
Field-Weighted Citation Impact
15.68

Funders

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article

LEAP-008: Lenvatinib Plus Pembrolizumab for Metastatic NSCLC That Has Progressed After an Anti–Programmed Cell Death Protein 1 or Anti–Programmed Cell Death Ligand 1 Plus Platinum Chemotherapy

Helena Linardou, Alexey Smolin, Rina Hui, Adam J. Schoenfeld et al.
15 citations
Journal of Thoracic Oncology
Cancer Immunotherapy and Biomarkers
15.68
article

LEAP-008: Lenvatinib Plus Pembrolizumab for Metastatic NSCLC That Has Progressed After an Anti–Programmed Cell Death Protein 1 or Anti–Programmed Cell Death Ligand 1 Plus Platinum Chemotherapy

Helena Linardou, Alexey Smolin, Rina Hui, Adam J. Schoenfeld, Natasha B. Leighl, Chinyere E. Okpara, Sofia Baka, Debra Kush, Ashwini Arunachalam, Vincenzo Di Noia, Luis Paz‐Ares, Diego Cortinovis, Delvys Rodríguez‐Abreu, Corina E. Dutcus, Byoung Chul Cho, Frédéric Bigot, Justin F. Gainor, Xuan Deng, Andrew Song, Samreen Ahmed, Makoto Nishio, Sameh Daher
article en
15 citations

Abstract

Lenvatinib plus pembrolizumab did not improve efficacy versus docetaxel in participants with stage IV NSCLC that progressed on anti‒programmed cell death protein 1 or anti-programmed cell death ligand 1 therapy and platinum-containing chemotherapy. There were no unexpected safety signals. More effective therapies are needed for this patient population.

Journal of Thoracic OncologyVol. 20(10)
Universidad de Las Palmas de Gran Canaria (ES), Merck & Co., Inc., Rahway, NJ, USA (United States) (US), Memorial Sloan Kettering Cancer Center (US), Yonsei University (KR), Hospital Universitario Insular de Gran Canaria (ES), Interbalkan Medical Center (GR), Massachusetts General Hospital (US), Hospital Universitario 12 De Octubre (ES), Institut de Cancérologie de l'Ouest (FR), Burdenko Neurosurgery Institute (RU), Eisai (United Kingdom) (GB), Metropolitan Hospital (GR), Eisai (United States) (US), Istituti di Ricovero e Cura a Carattere Scientifico (IT), Japanese Foundation For Cancer Research (JP)
Eisai
Openalex Percentile: Top 1%
Cancer Immunotherapy and Biomarkers
15.68
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