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Dostarlimab or pembrolizumab plus chemotherapy in previously untreated metastatic non-squamous non-small cell lung cancer: the randomized PERLA phase II trial

Authors
 Lim, Sun Min  ;  Peters, Solange  ;  Granados, Ana Laura Ortega  ;  Pinto, Gustavo dix Junqueira  ;  Fuentes, Christian Sebastian  ;  Lo Russo, Giuseppe  ;  Schenker, Michael  ;  Ahn, Jin Seok  ;  Reck, Martin  ;  Szijgyarto, Zsolt  ;  Huseinovic, Neda  ;  Zografos, Eleftherios  ;  Buss, Elena  ;  Stjepanovic, Neda  ;  ODonnell, Sean  ;  de Marinis, Filippo 
Citation
 NATURE COMMUNICATIONS, Vol.14(1), 2023-11 
Article Number
 7301 
Journal Title
NATURE COMMUNICATIONS
ISSN
 2041-1723 
Issue Date
2023-11
Abstract
PERLA is a global, double-blind, parallel phase II trial (NCT04581824) comparing efficacy and safety of anti-PD-1 antibodies dostarlimab and pembrolizumab, plus chemotherapy (DCT and PCT, respectively) as first-line treatment in patients with metastatic non-squamous NSCLC without known targetable genomic aberrations. Patients stratified by PD-L1 tumor proportion score and smoking status were randomized 1:1, receiving <= 35 cycles 500 mg dostarlimab or 200 mg pembrolizumab, <= 35 cycles 500 mg/m2 pemetrexed and <= 4 cycles cisplatin (75 mg/m2) or carboplatin (AUC 5 mg/ml/min) Q3W. Primary endpoint was overall response rate (ORR) (blinded independent central review). Secondary endpoints include progression-free survival (PFS) based on investigator assessment, overall survival (OS) and safety. Exploratory endpoints include ORR by PD-L1 subgroup and duration of response. PERLA met its pre-specified endpoint. ORR (n/N; 95% CI) is 45% (55/121; 36.4-54.8) for DCT and 39% (48/122; 30.6-48.6) for PCT (data cut-off: 07 July 23), numerically favoring dostarlimab in PD-L1-positive subgroups. Median PFS (months [95% CI]) is 8.8 (6.7-10.4) for DCT and 6.7 (4.9-7.1) for PCT (HR 0.70 [95% CI: 0.50-0.98]; data cut-off: 04 August 22). Median OS (months [95% CI]) is 19.4 (14.5-NR) for DCT and 15.9 (11.6-19.3) for PCT (HR 0.75 [95% CI: 0.53-1.05]) (data cut-off: 07 July 23). Safety profiles are similar between groups. In this study, DCT shows similar efficacy to PCT and demonstrates clinical efficacy as first-line treatment for patients with metastatic non-squamous NSCLC. Several PD-(L)1 inhibitors have been approved or are in development for the treatment of NSCLC, showing promising efficacy and tolerable safety profiles. Here, the authors present a randomized phase II clinical trial comparing two different anti-PD-1 antibodies, dostarlimab and pembrolizumab, both combined with chemotherapy as first-line treatment in patients with metastatic NSCLC.
DOI
10.1038/s41467-023-42900-4
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Yim, Sun Mie(임선미)
Lim, Sun Min(임선민)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/198024
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