Systemic treatment of immune checkpoint inhibitor‐induced psoriasis: Inference‐based guidance

Although there is no direct evidence, we support the following conclusions: saPs may be used to treat ICI-Ps without an appreciable loss of ICI effectiveness. Generally, it is not necessary to interrupt ICI therapy. When available, non-steroid saPs are preferred over systemic corticosteroids for the treatment of psoriasis.

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Publication Details

Journal
Journal of the European Academy of Dermatology and Venereology
Published
2025-07-21
DOI
https://doi.org/10.1111/jdv.20809
Citations
6
Primary Topic
Cancer Immunotherapy and Biomarkers
Type
article
Field-Weighted Citation Impact
6.27

Funders

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article

Systemic treatment of immune checkpoint inhibitor‐induced psoriasis: Inference‐based guidance

Kim Papp, Rosalyn A. Juergens, Joël Claveau, Jennifer Beecker et al.
6 citations
Journal of the European Academy of Dermatology and Venereology
Cancer Immunotherapy and Biomarkers
6.27
article

Systemic treatment of immune checkpoint inhibitor‐induced psoriasis: Inference‐based guidance

Kim Papp, Rosalyn A. Juergens, Joël Claveau, Jennifer Beecker, L. Puig, Jan Dutz, Stephanie Snow, Javier Cortés, Sandeep R. Sehdev, Maxwell Benjamin Sauder, V. Sibaud, Barbara Melosky, Anisha B. Patel, Noah I. Hornick, Vinod Chandran
article en
6 citations

Abstract

Although there is no direct evidence, we support the following conclusions: saPs may be used to treat ICI-Ps without an appreciable loss of ICI effectiveness. Generally, it is not necessary to interrupt ICI therapy. When available, non-steroid saPs are preferred over systemic corticosteroids for the treatment of psoriasis.

Journal of the European Academy of Dermatology and VenereologyVol. 39(11)
Universitat Autònoma de Barcelona (ES), BC Cancer Agency (CA), Dalhousie University (CA), University Health Network (CA), The University of Texas MD Anderson Cancer Center (US), University of British Columbia (CA), University of Ottawa (CA), Oregon Health & Science University (US), University of Toronto (CA), Juravinski Cancer Centre (CA), Ottawa Hospital (CA), Hospital de Sant Pau (ES), Villa Maria Hospital (UG), Vancouver General Hospital (CA), Research Canada (CA), MedSIR (Spain) (ES), Hôtel-Dieu de Québec (CA), Probity Medical Research (CA), Institut Claudius Regaud (FR), Krembil Foundation (CA), Blackberry (Canada) (CA), BC Children's Hospital (CA), International Breast Cancer Study Group (CH), The University of Texas Health Science Center (US), Institut de Recerca Sant Pau (ES), Krembil Research Institute, Ottawa Hospital Research Institute (CA), Universidad Europea de Madrid (ES), The University of Texas Health Science Center at Houston (US), McMaster University (CA)
Amgen, Bristol-Myers Squibb, Eli Lilly and Company, Pfizer, AstraZeneca, Sanofi, L'Oreal USA, Melanoma Research Alliance, Gilead Sciences, Ariad Pharmaceuticals, Celgene, Therakos, Queen Mary University of London, Regeneron Pharmaceuticals, Jazz Pharmaceuticals, BC Children's Hospital, Les Laboratories Pierre Fabre, Clovis Oncology, BeiGene, Incyte, MacroGenics, Seagen, Eisai, Astellas Pharma, Galderma, Servier, Sun Pharma, Bausch Health, LEO Pharma, National Institutes of Health, Samsung, EMD Serono, University of Texas MD Anderson Cancer Center, Novartis Pharmaceuticals Canada, Amgen Canada, Sanofi Genzyme, Eli Lilly Canada, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Center for Advancing Translational Sciences, Janssen Pharmaceuticals, Janssen Canada, Daiichi Sankyo Europe
Openalex Percentile: Top 3%
Cancer Immunotherapy and Biomarkers
6.27
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