| Literature DB >> 35253011 |
Melissa Neumann1, Neal Murphy2, Nagashree Seetharamu2.
Abstract
Non-small cell lung cancer (NSCLC) was traditionally associated with a poor prognosis. Between 2010 and 2016, the 5-years overall survival for all stages combined was about 25 percent. However, the recent use of immunotherapy has led to significant improvements in progression free survival (PFS) and overall survival (OS). Immune check point inhibitors enable the host immune system to mount a lethal response against tumor cells. Both PD-1 (nivolumab, pembrolizumab, cemipilimab) and PD-L1 inhibitors (atezolizumab and durvalumab) have been approved by the FDA for use in NSCLC, either as individual agents or in combination with platinum-based chemotherapy, radiation therapy, or other agents. As the future of immunotherapy for lung cancer continues to evolve, with multiple agents approved or in various stages of clinical research, it is imperative that we understand the mechanism of action, clinical activity, ongoing clinical trials, indications for use and toxicity for individual agents in addition to having general, basic knowledge about this new class of cancer therapeutics. In this review, we focus on two of the newer PD-L1 inhibitors, durvalumab and avelumab.Entities:
Keywords: Atezolizumab; Avelumab; Durvalumab; Immune checkpoint inhibitor; Non-small cell lung cancer; PD-1 inhibitor; PD-L1 inhibitor
Year: 2021 PMID: 35253011 PMCID: PMC8896901
Source DB: PubMed Journal: Cancer Med J