AI Article Synopsis

  • Immune checkpoint inhibitors like ipilimumab show promise for treating metastatic melanoma in kidney transplant recipients, but data on their safety and efficacy are limited.
  • Six French patients (mean age 66) were studied, experiencing minimal adverse effects; however, one patient faced acute T cell-mediated rejection post-treatment.
  • Despite some patients showing stable disease, all ultimately died, suggesting that while ipilimumab may be safe, a reduction in immunosuppression could increase rejection risks without significantly benefiting cancer treatment.

Article Abstract

Immune checkpoint inhibitors are new therapeutic options for metastatic melanoma, but few data are available in organ transplant recipient populations. Six French patients, three men and three women, mean age 66 years (range 44-74), all kidney transplant recipients, received ipilimumab (CTLA-4 inhibitor) for metastatic melanoma. At diagnosis of advanced melanoma, immunosuppressive therapy had been minimized in all but one. Adverse effects included one case of grade 1 diarrhea and one of grade 1 pruritus. One patient had acute T cell-mediated rejection confirmed by histology after the first injection of ipilimumab. After a median follow-up of 4.5 (3-20) months, one patient achieved partial response, one had stable disease, and four had disease progression. All the patients died, five from melanoma, one from another cause. In this series and in the literature, ipilimumab proved to be safe and possibly active. The acute rejection we encountered was probably related to both a rapid, drastic reduction of immunosuppression and the use of ipilimumab. Our safety data on ipilimumab contrast with the organ transplant rejections already reported with PD-1 inhibitors. We consider that immunosuppression should not be minimized, as the impact on metastatic disease control is probably small.

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Source
http://dx.doi.org/10.1111/ajt.15071DOI Listing

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