| Literature DB >> 32360716 |
Samantha R Ellis1, Aren T Vierra2, Jillian W Millsop3, Mario E Lacouture4, Maija Kiuru5.
Abstract
Antineoplastic agents that use the immune system have revolutionized cancer treatment. Specifically, implementation of immune checkpoint inhibitors, monoclonal antibodies that block cytotoxic T-lymphocyte-associated antigen-4, programmed cell death protein 1, or programmed cell death ligand 1 show improved and sustained responses in patients with cancer. However, these agents are associated with a plethora of adverse events, many manifesting in the skin. As the clinical application of cancer immunotherapies expands, understanding the clinical and histopathologic features of associated cutaneous toxicities becomes increasingly important to dermatologists, oncologists, and pathologists to ensure timely diagnosis and appropriate care. This review discusses cutaneous reactions to immune checkpoint inhibitors, focusing on histopathologic features.Entities:
Keywords: CTLA-4; PD-L1; PD1; adverse event; atezolizumab; avelumab; bullous pemphigoid; checkpoint inhibitor; cutaneous; durvalumab; immunotherapy; ipilimumab; lichenoid dermatitis; nivolumab; pembrolizumab; rash; skin; toxicity
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Year: 2020 PMID: 32360716 PMCID: PMC7492441 DOI: 10.1016/j.jaad.2020.04.105
Source DB: PubMed Journal: J Am Acad Dermatol ISSN: 0190-9622 Impact factor: 11.527