| Literature DB >> 31308203 |
Shahin Jamal1,2, Marie Hudson3,4, Aurore Fifi-Mah3,4, Carrie Ye3,4.
Abstract
Immune checkpoint inhibitors have revolutionized cancer therapy by blocking inhibitory pathways of the immune system to fight cancer cells. Their use is often limited by the development of autoimmune toxicities, which can affect multiple organ systems and are referred to as immune-related adverse events (irAE). Among these are rheumatologic irAE, including inflammatory arthritis, myositis, vasculitis, and others. Rheumatologic irAE seem to be different from irAE in other organs and from traditional autoimmune diseases in that they can occur early or have delayed onset, and can persist chronically, even after cancer therapy is terminated. Because immune checkpoint inhibitors are increasingly used for many types of cancer, it is important for oncologists and rheumatologists to recognize and manage toxicities early. In this review, we discuss currently approved immune checkpoint inhibitors and their mechanisms of action and systemic toxicities, with a focus on the management and effect on further cancer therapy of rheumatic irAE.Entities:
Keywords: ADVERSE EVENTS; IMMUNE CHECKPOINT INHIBITORS; IMMUNOTHERAPY; INFLAMMATORY ARTHRITIS; MYOSITIS; VASCULITIS
Mesh:
Substances:
Year: 2019 PMID: 31308203 DOI: 10.3899/jrheum.190084
Source DB: PubMed Journal: J Rheumatol ISSN: 0315-162X Impact factor: 4.666