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Efficacy of Pembrolizumab Monotherapy in Patients with or without Brain Metastases from Advanced Non-Small Cell Lung Cancer with a PD-L1 Expression ≥50%

Academic Article
Publication Date:
2020
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.
Iris type:
1.1 Articolo in rivista
Keywords:
brain metastases; immunotherapy; non-small cell lung cancer; PD-L1≥50%; pembrolizumab; Antibodies; Monoclonal; Humanized; B7-H1 Antigen; Brain Neoplasms; Carcinoma; Non-Small-Cell Lung; Disease Management; Female; Humans; Immune Checkpoint Inhibitors; Lung Neoplasms; Male; Molecular Targeted Therapy; Neoplasm Staging; Prognosis; Treatment Outcome
List of contributors:
Metro, G.; Banna, G. L.; Signorelli, D.; Gili, A.; Galetta, D.; Galli, G.; Economopoulou, P.; Roila, F.; Friedlaender, A.; Camerini, A.; Christopoulou, A.; Cantale, O.; De Toma, A.; Pizzutilo, P.; Jimenez, B.; Collazo-Lorduy, A.; Calles, A.; Baxevanos, P.; Linardou, H.; Kosmidis, P.; Giannarelli, D.; Mountzios, G.; Addeo, A.
Authors of the University:
GILI ALESSIO
Handle:
https://iris.unilink.it/handle/20.500.14085/22704
Published in:
JOURNAL OF IMMUNOTHERAPY
Journal
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