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Clinicopathologic correlates of first-line pembrolizumab effectiveness in patients with advanced NSCLC and a PD-L1 expression of ≥ 50%

Authors :
Giovanni Mansueto
Lorenza Landi
Francesco Grossi
Cinzia Baldessari
Michele De Tursi
Alessio Cortellini
Vincenzo Sforza
Alain Gelibter
Raffaele Giusti
Biagio Ricciuti
Giuseppe Luigi Banna
Daniele Santini
Giorgia Guaitoli
Joachim G.J.V. Aerts
Russano Marco
Rita Chiari
Ornella Cantale
Luca Sala
Mariangela Torniai
Stefania Gori
Claudia Proto
Luigi Della Gravara
Diego Signorelli
Lorenzo Antonuzzo
Emilio Bria
Francesco Passiglia
Serena Ricciardi
Luca Cantini
Corrado Ficorella
Simona Carnio
Annamaria Catino
Paola Bordi
Vincenzo Di Noia
Miriam Grazia Ferrara
Maria Giovanna Dal Bello
Domenico Galetta
Sebastiano Buti
Federica Zoratto
Giampiero Porzio
Marianna Tudini
Paolo Marchetti
Diego Cortinovis
Erika Rijavec
Matteo Santoni
Carlo Genova
Danilo Rocco
Alex Friedlaender
Robert A. Belderbos
Ettore D'Argento
Simona Scodes
Pamela Pizzutilo
Marcello Tiseo
Alfredo Addeo
Marianna Macerelli
Rossana Berardi
Giada Targato
Federico Cappuzzo
Francesca Mazzoni
Alessandro Morabito
Fabrizio Citarella
Maria Rita Migliorino
Alessandro De Toma
Olga Nigro
Paolo Bironzo
Fausto Barbieri
Marco Filetti
Alessandro Tuzi
Giulio Metro
Francesca Rastelli
Alessio Grieco
Pulmonary Medicine
Source :
Cancer Immunology, Immunotherapy, 69(11), 2209-2221. Springer Science+Business Media
Publication Year :
2020
Publisher :
Springer Science and Business Media Deutschland GmbH, 2020.

Abstract

Single-agent pembrolizumab represents the standard first-line option for metastatic non-small-cell lung cancer (NSCLC) patients with a PD-L1 (programmed death-ligand 1) expression of ≥ 50%. We conducted a multicenter retrospective study aimed at evaluating the clinicopathologic correlates of pembrolizumab effectiveness in patients with treatment-naive NSCLC and a PD-L1 expression of ≥ 50%. One thousand and twenty-six consecutive patients were included. The objective response rate (ORR) was 44.5% (95% CI 40.2–49.1), while the median progression free survival (PFS) and overall survival (OS) were 7.9 months (95% CI 6.9–9.5; 599 events) and 17.2 months (95% CI 15.3–22.3; 598 censored patients), respectively. ECOG-PS ≥ 2 (p

Details

Language :
English
ISSN :
03407004
Database :
OpenAIRE
Journal :
Cancer Immunology, Immunotherapy, 69(11), 2209-2221. Springer Science+Business Media
Accession number :
edsair.doi.dedup.....299351854891d785717f66ecb3cc59b1