Ipilimumab in the treatment of metastatic melanoma: management of adverse events
- PMID: 24570590
- PMCID: PMC3933725
- DOI: 10.2147/OTT.S57335
Ipilimumab in the treatment of metastatic melanoma: management of adverse events
Abstract
Recently, "ipilimumab," an anti-cytotoxic T-lymphocyte antigen-4 (CTLA-4) monoclonal antibody, has been demonstrated to improve overall survival in metastatic melanoma. "CTLA-4" is an immune-checkpoint molecule that downregulates pathways of T-cell activation. Ipilimumab, by targeting CTLA-4, is able to remove the CTLA-4 inhibitory signal, allowing the immune system to react to cancer cells. Due to its immune-based mechanism of action, ipilimumab causes the inhibition of CTLA-4-mediated immunomodulatory effects, the enhancement of antitumor specific immune response mediated by the weakening of self-tolerance mechanisms while exacerbating the development of autoimmune diseases and immune-related adverse events, including dermatitis, hepatitis, enterocolitis, hypophysitis, and uveitis.
Keywords: CTLA-4; T-cells; adverse events; autoimmunity; melanoma.
References
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- Bristol-Myers Squibb MDX-010 Antibody, MDX-1379 Melanoma Vaccine, or MDX-010/MDX-1379 Combination Treatment for Patients With Unresectable or Metastatic Melanoma. [Accessed January 22, 2014]. Available from: http://clinicaltrials.gov/show/NCT00094653. NLM identifier: NCT00094653.
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- Bristol-Myers Squibb Dacarbazine and Ipilimumab vs. Dacarbazine With Placebo in Untreated Unresectable Stage III or IV Melanoma. [Accessed January 22, 2014]. Available from: http://clinicaltrials.gov/show/NCT00324155. NLM identifier: NCT00324155.
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