Evidence map›Paper›PMID 40685883›Full record

SynthesisJournal of the European Academy of Dermatology and Venereology : JEADV2025

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

Kim A Papp, Luis Puig, Jennifer Beecker, Vinod Chandran, Joël Claveau, Javier Cortés, Jan Dutz, Noah I Hornick, Rosalyn A Juergens, Barbara Melosky and 5 more

Abstract readSystematic Review
In one paragraph

Synthesis in Journal of the European Academy of Dermatology and Venereology : JEADV, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Systemic treatment of immune checkpoint inhibitor-induced psoriasis: Inference-based guidance.Journal of the European Academy of Dermatology and Venereology : JEADV · 2025
    Pooled it
  2. Dermatologic Toxicities Induced by JAK Inhibitors.American journal of clinical dermatology · 2026
    Review
  3. Review
  4. Article
  5. IL-23 Inhibitors in Psoriasis: What Have We Learnt so Far?Journal of inflammation research · 2026
    Review
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Kim A PappProbity Medical Research Inc., Waterloo, Ontario, Canada.ORCID https://orcid.org/0000-0001-9557-3642
Luis PuigDepartment of Dermatology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.ORCID https://orcid.org/0000-0001-6083-0952
Jennifer BeeckerProbity Medical Research Inc., Waterloo, Ontario, Canada.
Vinod ChandranGladman-Krembil Psoriatic Arthritis Research Program, Centre for Prognosis Studies in the Rheumatic Diseases, Schroeder Arthritis Institute, Krembil Research Institute, University Health Network, Toronto, Ontario, Canada.
Joël ClaveauMelanoma and Skin Cancer Clinic, Hôtel-Dieu de Québec, et Centre Intégré de Cancérologie, Centre Hospitalier Universitaire de Québec, Quebec City, Quebec, Canada.
Javier CortésMedica Scientia Innovation Research (MEDSIR), Barcelona, Spain.
Jan DutzDepartment of Dermatology and Skin Science, Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
Noah I HornickDepartment of Dermatology, Oregon Health & Science University, Portland, Oregon, USA.
Rosalyn A JuergensDepartment of Oncology, Juravinski Cancer Centre, McMaster University, Hamilton, Ontario, Canada.
Barbara MeloskyDepartment of Medical Oncology, BC Cancer, Vancouver, British Columbia, Canada.
Anisha B PatelDepartment of Dermatology, MD Anderson Cancer Center, University of Texas, Houston, Texas, USA.
Maxwell B SauderProbity Medical Research Inc., Waterloo, Ontario, Canada.ORCID https://orcid.org/0000-0002-5605-3844
Sandeep SehdevThe Ottawa Hospital Cancer Centre, Ottawa, Ontario, Canada.
Vincent SibaudDepartment of Oncodermatology, Oncopole Claudius Regaud, Toulouse, France.ORCID https://orcid.org/0000-0003-2585-6633
Stephanie L SnowDivision of Medical Oncology, Department of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada.

Funding

Oregon Clinical and Translational Research Institute KL2 SupplementKL2TR002370 · NCATS · OREGON HEALTH & SCIENCE UNIVERSITY · PI Catherine Lee Hough · 2017 to 2026
$10.1M
Amgen CanadaArcutis BiotherapeuticsBausch HealthEli Lilly CanadaJanssen CanadaNCATS NIH HHS KL2 TR002370Novartis Pharmaceuticals CanadaUCB Canada
6 · The paper itself

Abstract

backgroundImmune checkpoint inhibitors (ICIs) are increasingly used to treat various cancers. Their use may result in immune-related adverse events, including psoriasis. When managing psoriasis, induced or exacerbated by an ICI, there are concerns regarding immunosuppression from systemic agents for the treatment of psoriasis (saPs) and the potential impact on ICI efficacy. No direct, high-level evidence exists to address these concerns.

objectiveTo address clinically relevant questions regarding the management of ICI-mediated psoriasis (ICI-Ps) with saPs.

methodsWe convened a multidisciplinary panel of 15 international specialists in dermatology, oncology, immunology, and rheumatology. A Delphi process defined clinical concerns related to the systemic treatment of ICI-Ps, focusing on the potential of saPs to impact ICI effectiveness. The saPs considered included biologics targeting tumour necrosis factor, interleukin (IL)-17, IL-12/23 and IL-23, traditional systemic therapies (cyclosporine, methotrexate), small molecules targeting phosphodiesterase-4 or tyrosine kinase 2, systemic retinoids (acitretin), and systemic corticosteroids. A systematic review of the literature was supplemented with evidence supporting an inference-based methodology to derive conclusions on the use of systemic therapies in patients with ICI-Ps. The specialist panel rated the strength of the conclusions using a probabilistic scale.

resultsAfter reviewing the totality of direct and indirect evidence, we drafted inference-based conclusions and ascribed a level of support, focusing on the potential impact of saPs on ICI efficacy. This work provides a structured framework informing healthcare professional and patient discussions on the risks and benefits of using saPs in patients with cancer who experience ICI-Ps.

conclusionsAlthough 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.

Indexed as

Immune Checkpoint InhibitorsPsoriasisDelphi TechniqueHumansImmune Checkpoint Inhibitorsatezolizumabavelumabcemiplimabdostarlimabdurvalumabguidelineimmune checkpoint inhibitorsimmune‐related adverse eventsimmunomodulating agentsimmunosuppressive agentsipilimumabnivolumabpembrolizumabpsoriasis

Identifiers

PMID40685883
PMCPMC12553135

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.