Phase 1 expansion cohort of ramucirumab plus pembrolizumab in advanced treatment-naive NSCLC

Introduction - Data of first-line ramucirumab plus pembrolizumab treatment of programmed death-ligand 1 (PD-L1)-positive NSCLC (cohort E) are reported (NCT02443324). - Methods - In this multicenter, open-label phase 1a/b trial, patients received ramucirumab 10 mg/kg and pembrolizumab 200 mg every 21...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Herbst, Roy S. (VerfasserIn) , Arkenau, Hendrik Tobias (VerfasserIn) , Bendell, Johanna (VerfasserIn) , Arrowsmith, Edward (VerfasserIn) , Wermke, Martin (VerfasserIn) , Soriano, Andres (VerfasserIn) , Penel, Nicolas (VerfasserIn) , Santana-Davila, Rafael (VerfasserIn) , Bischoff, Helge (VerfasserIn) , Chau, Ian (VerfasserIn) , Mi, Gu (VerfasserIn) , Wang, Hong (VerfasserIn) , Rasmussen, Erik (VerfasserIn) , Ferry, David (VerfasserIn) , Chao, Bo H. (VerfasserIn) , Paz-Ares, Luis (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 2021
In: Journal of thoracic oncology
Year: 2021, Jahrgang: 16, Heft: 2, Pages: 289-298
ISSN:1556-1380
DOI:10.1016/j.jtho.2020.10.004
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1016/j.jtho.2020.10.004
Verlag, lizenzpflichtig, Volltext: https://www.sciencedirect.com/science/article/pii/S1556086420308091
Volltext
Verfasserangaben:Roy S. Herbst, MD, PhD, Hendrik Tobias Arkenau, MD, Johanna Bendell, MD, Edward Arrowsmith, MD, Martin Wermke, MD, Andres Soriano, MD, Nicolas Penel, MD, Rafael Santana-Davila, MD, Helge Bischoff, MD, Ian Chau, MD, Gu Mi, PhD, Hong Wang, PhD, Erik Rasmussen, PhD, David Ferry, MD, Bo H. Chao, MD, Luis Paz-Ares, MD
Beschreibung
Zusammenfassung:Introduction - Data of first-line ramucirumab plus pembrolizumab treatment of programmed death-ligand 1 (PD-L1)-positive NSCLC (cohort E) are reported (NCT02443324). - Methods - In this multicenter, open-label phase 1a/b trial, patients received ramucirumab 10 mg/kg and pembrolizumab 200 mg every 21 days for up to 35 cycles. PD-L1 positivity was defined as tumor proportion score (TPS) greater than or equal to 1%. Exploratory NanoString biomarker analyses included three T-cell signatures (T-cell-inflamed, Gajewski, and effector T cells) and CD274 gene expression. - Results - Cohort E included 26 patients. Treatment-related adverse events of any grade occurred in 22 patients (84.6%). Treatment-related adverse events of grade greater than or equal to 3 were reported in 11 patients (42.3%); the most frequent was hypertension (n = 4, 15.4%). Objective response rate was 42.3% in the treated population and 56.3% and 22.2% for patients with high (TPS ≥ 50%) and lower levels (TPS 1%-49%) of PD-L1 expression, respectively. Median progression-free survival (PFS) in the treated population was 9.3 months, and 12-month and 18-month PFS rates were 45% each. Median PFS was not reached in patients with PD-L1 TPS greater than or equal to 50% and was 4.2 months in patients with PD-L1 TPS 1% to 49%. Median overall survival was not reached in the treated population, and 12-month and 18-month overall survival rates were 73% and 64%, respectively. Biomarker data suggested a positive association among clinical response, three T-cell signatures, CD274 gene expression, and PD-L1 immunohistochemistry. - Conclusions - First-line therapy with ramucirumab plus pembrolizumab has a manageable safety profile in patients with NSCLC, and the efficacy signal seems to be strongest in tumors with high PD-L1 expression.
Beschreibung:Available online 15 October 2020
Gesehen am 12.05.2021
Beschreibung:Online Resource
ISSN:1556-1380
DOI:10.1016/j.jtho.2020.10.004