AI Article Synopsis

  • Switching from immunotherapy to targeted therapy in melanoma can lead to a serious complication known as cytokine release syndrome (CRS), which is caused by elevated cytokines and affects various organs.
  • Two patients with BRAF V600 mutant melanoma experienced CRS after switching from anti-PD-1 and anti-LAG-3 antibodies to BRAF/MEK inhibitors due to disease progression.
  • The cases highlight the challenges of managing interactions between immune checkpoint inhibitors and kinase inhibitors, emphasizing the importance of early detection and management of CRS to enhance safety in subsequent treatments.

Article Abstract

Switching from immunotherapy to targeted therapy in metastasized melanoma can be complicated by a cytokine release syndrome (CRS). CRS is a serious complication, which is induced by high levels of circulating cytokines, associated with T-cell engagement and proliferation, and results in a constellation of symptoms with variable organ involvement. We report 2 patients with BRAF V600 mutant melanoma who were previously treated with anti-PD-1±anti-LAG-3 antibodies and were switched to BRAF/MEK-inhibitors because of progressive disease. Both cases depict the complexity of interactions occurring during sequential treatment with immune checkpoint inhibitors and kinase inhibitors. Early identification and management of CRS is crucial to decrease its toxicity and improve safety of further drugs to be given in a therapeutic ladder.

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Source
http://dx.doi.org/10.1097/CJI.0000000000000236DOI Listing

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