Journal
JOURNAL OF IMMUNOTHERAPY
Volume 43, Issue 9, Pages 299-306Publisher
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/CJI.0000000000000340
Keywords
brain metastases; immunotherapy; non-small cell lung cancer; PD-L1 >= 50%; pembrolizumab
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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.
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