4.6 Article

Nivolumab: A Review in Advanced Squamous Non-Small Cell Lung Cancer

Journal

DRUGS
Volume 75, Issue 16, Pages 1925-1934

Publisher

ADIS INT LTD
DOI: 10.1007/s40265-015-0492-9

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Nivolumab (Opdivo (R); Nivolumab BMS (TM)) was the first programmed death (PD)-1 immune checkpoint inhibitor to be approved for use in advanced, squamous non-small cell lung cancer (NSCLC) following prior chemotherapy. In the pivotal CheckMate 017 trial, intravenous nivolumab 3 mg/kg every 2 weeks was associated with significantly better overall survival and progression-free survival and a significantly higher overall response rate than intravenous docetaxel in the second-line treatment of advanced, squamous NSCLC. Nivolumab was also better tolerated than docetaxel in CheckMate 017, and its adverse event profile (which included immune-mediated adverse events) was manageable. In conclusion, nivolumab represents an important advance in previously-treated, advanced, squamous NSCLC.

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