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Steroid-Refractory Immune-Related Adverse Events Induced by Checkpoint Inhibitors.
Tomsitz, Dirk; Ruf, Theresa; Zierold, Sarah; French, Lars E; Heinzerling, Lucie.
  • Tomsitz D; Department of Dermatology and Allergy, University Hospital, LMU Munich, 80539 Munich, Germany.
  • Ruf T; Department of Dermatology and Allergy, University Hospital, LMU Munich, 80539 Munich, Germany.
  • Zierold S; SERIO Side Effects Registry Immunooncology, 80337 Munich, Germany.
  • French LE; Department of Dermatology and Allergy, University Hospital, LMU Munich, 80539 Munich, Germany.
  • Heinzerling L; SERIO Side Effects Registry Immunooncology, 80337 Munich, Germany.
Cancers (Basel) ; 15(9)2023 Apr 28.
Article en En | MEDLINE | ID: mdl-37174003
ABSTRACT
The occurrence, second-line management and outcome of sr/sd-irAEs was investigated in patients with skin cancer. All skin cancer patients treated with immune checkpoint inhibitors (ICIs) between 2013 and 2021 at a tertiary care center were analyzed retrospectively. Adverse events were coded by CTCAE version 5.0. The course and frequency of irAEs were summarized using descriptive statistics. A total of 406 patients were included in the study. In 44.6% (n = 181) of patients, 229 irAEs were documented. Out of those, 146 irAEs (63.8%) were treated with systemic steroids. Sr-irAEs and sd-irAEs (n = 25) were detected in 10.9% of all irAEs, and in 6.2% of ICI-treated patients. In this cohort, infliximab (48%) and mycophenolate mofetil (28%) were most often administered as second-line immunosuppressants. The type of irAE was the most important factor associated with the choice of second-line immunosuppression. The Sd/sr-irAEs resolved in 60% of cases, had permanent sequelae in 28% of cases, and required third-line therapy in 12%. None of the irAEs were fatal. Although these side effects manifest in only 6.2% of patients under ICI therapy, they impose difficult therapy decisions, especially since there are few data to determine the optimal second-line immunosuppression.
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Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Año: 2023 Tipo del documento: Article