| Literature DB >> 32991393 |
Giulio Metro1, Giuseppe Luigi Banna2, Diego Signorelli3, Alessio Gili4, Domenico Galetta5, Giulia Galli3, Panagiota Economopoulou6, Fausto Roila1, Alex Friedlaender7, Andrea Camerini8, Athina Christopoulou9, Ornella Cantale2, Alessandro De Toma3, Pamela Pizzutilo5, Beatriz Jimenez10, Ana Collazo-Lorduy10, Antonio Calles11, Panagiotis Baxevanos12, Helena Linardou13, Paris Kosmidis14, Diana Giannarelli15, Giannis Mountzios16, Alfredo Addeo7.
Abstract
The authors conducted a multicenter retrospective study on the outcome of programmed death-ligand 1 tumor proportion score≥50% advanced non-small cell lung cancer patients treated with first-line pembrolizumab according to the presence/absence of brain metastases. A total of 282 patients were included, of whom 56 had brain metastases that were treated with upfront local radiation therapy in 80.3% of cases. The overall response rate was 39.2% and 44.4% in patients with and without brain metastases (P=0.48), respectively, while intracranial response rate and intracranial disease control rate were 67.5% and 85.0%, respectively. The median time-to-treatment failure (TTF) and overall survival (OS) were 4.2 and 9.9 months versus 10.8 and 26.5 months for patients with and without brain metastases (P=0.06 and 0.05, respectively). Drug discontinuation rate due to treatment-related adverse events was 10.7% and 10.2% in patients with and without brain metastases, respectively. Multivariate analysis showed that baseline steroids was an independent predictor for a worse OS (P<0.001), while performance status (PS)≥2 was an independent predictor for a poorer TTF (P<0.001) and OS (P<0.001). In patients with brain metastases, only PS ≥2 was predicted for a worse TTF (P=0.02) and OS (P=0.03). Pembrolizumab has activity against brain metastases from non-small cell lung cancers with programmed death-ligand 1≥50%. Presence of brain metastases per se does not appear to be prognostic, and PS ≥2 seems to be the only factor associated with a worse outcome in patients with brain metastases.Entities:
Year: 2020 PMID: 32991393 DOI: 10.1097/CJI.0000000000000340
Source DB: PubMed Journal: J Immunother ISSN: 1524-9557 Impact factor: 4.456