| Literature DB >> 28923211 |
Vinay Prasad1, Victoria Kaestner2.
Abstract
Nivolumab (Opdivo, Bristol Meyer Squibb, New York, NY) and pembrolizumab (Keytruda, Merck, Kenilworth, NJ) are the first two US Food and Drug Administration (FDA)-approved monoclonal antibodies targeting programmed death-1 (PD-1). Nivolumab and pembrolizumab work by interfering with the interaction between PD-1 and programmed death ligand-1 (PD-L1), whose unimpeded interaction downregulates T cells allowing cancer cells to evade immune surveillance. These drugs have earned a series of FDA approvals for melanoma, non-small cell lung cancer (NSCLC), head and neck squamous cell cancer (HNSCC), urothelial cancer, classical Hodgkin lymphoma, and renal cell cancer. In this review we will summarize the data for efficacy and toxicity for these two agents. We conclude that they represent two valuable but interchangeable alternatives to target their approved indications. We will discuss how this can help global payers seeking to contain the cost of cancer therapeutics that continues to spiral out of control.Entities:
Keywords: Drug manufacturing; Me-too drugs; Nivolumab; Pembrolizumab
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Year: 2017 PMID: 28923211 DOI: 10.1053/j.seminoncol.2017.06.007
Source DB: PubMed Journal: Semin Oncol ISSN: 0093-7754 Impact factor: 4.929