Immune Checkpoint Inhibitor Toxicities.

Mayo Clin Proc

Division of Hematology and Medical Oncology, Mayo Clinic, Jacksonville, FL. Electronic address:

Published: July 2019

AI Article Synopsis

  • - Immune checkpoint inhibitors boost the body's immune response to fight tumors, transforming cancer treatment since their success in advanced melanoma and now being used for other cancers.
  • - These therapies can lead to immune-related adverse events, which manifest as autoimmune-like toxicities affecting various organs, with skin and colon being the most common sites.
  • - Management of these adverse effects often involves corticosteroids or other immunosuppressive treatments, and may necessitate stopping immunotherapy based on the toxicity severity.

Article Abstract

Immune checkpoint inhibitors are molecules that increase the endogenous immune response against tumors. They have revolutionized the field of oncology. Since their initial approval for the treatment of advanced melanoma, their use has expanded to the treatment of several other advanced cancers. Unfortunately, immune checkpoint inhibitors have also been associated with the emergence of a new subset of autoimmune-like toxicities, known as immune-related adverse events. These toxicities differ depending on the agent, malignancy, and individual susceptibilities. Although the skin and colon are most commonly involved, any organ may be affected, including the liver, lungs, kidneys, and heart. Most of these toxicities are diagnosed by excluding other secondary infectious or inflammatory causes. Corticosteroids are commonly used for treatment of moderate and severe immune-related adverse events, although additional immunosuppressive therapy may occasionally be required. The occurrence of immune-related toxicities may require discontinuation of immunotherapy, depending on the specific toxicity and its severity. In this article, we provide a focused review to familiarize practicing clinicians with this important topic given that the use of immune checkpoint inhibitors continues to increase.

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Source
http://dx.doi.org/10.1016/j.mayocp.2019.03.012DOI Listing

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