4.7 Article

Safety and efficacy of durvalumab (MEDI4736) in various solid tumors

Journal

DRUG DESIGN DEVELOPMENT AND THERAPY
Volume 12, Issue -, Pages 2085-2096

Publisher

DOVE MEDICAL PRESS LTD
DOI: 10.2147/DDDT.S162214

Keywords

durvalumab; solid cancers; adverse effects; efficacy; meta-analysis

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Introduction: The prominent immune checkpoint molecule, programmed cell death ligand-1 (PD-L1), is the object of increasing attention. Here, we report a meta-analysis investigating the safety and efficacy of durvalumab (MEDI4736), an inhibitor of PD-L1, in various solid tumors. Methods: A systematic search of PubMed, Embase, and related articles was performed. Safety data were analyzed using Comprehensive Meta-Analysis software program version 2. Ultimately. 17 studies with 1,529 patients were included in our analysis. Results: The major adverse events associated with durvalumab were pruritus and fatigue, while pruritus, increased alanine transaminase, and increased aspartate aminotransferase were common among patients treated with a combination of durvalumab and tremelimumab. Higher PD-L1 expression was associated with a superior objective response rate. Conclusion: Durvalumab is safe in patients with many solid cancers and, in combination with tremelimumab, it has a tolerable safety profile and is associated with improved prognosis. PD-L1 expression is a biomarker of the efficacy of durvalumab.

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