Evidence map›Paper›PMID 39925013›Full record

ArticleInternational journal of dermatology2025

Cutaneous Side Effects of PD-1 Inhibitors: A Single-Center Retrospective Study.

Melánia Pozsgai, Udoh Frieda-Rex Sebastian, Péter Oláh, Viktória Németh, Rolland Gyulai, Zsuzsanna Lengyel

Abstract read
In one paragraph

Article in International journal of dermatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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

  1. Diagnosis and management of immune checkpoint inhibitor-induced dry mouth and salivary gland dysfunction in oncology patients: a systematic review.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2026
    Pooled it
  2. Article
  3. Review
  4. Review
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

6 authors.

Melánia PozsgaiDepartment of Dermatology, Venerology and Oncodermatology Clinical Center, University of Pécs, Pécs, Hungary.ORCID https://orcid.org/0009-0001-4990-1366
Udoh Frieda-Rex SebastianMalta Foundation Program, Mater Dei Hospital, Msida, Malta.
Péter OláhDepartment of Dermatology, Venerology and Oncodermatology Clinical Center, University of Pécs, Pécs, Hungary.
Viktória NémethDepartment of Dermatology, Venerology and Oncodermatology Clinical Center, University of Pécs, Pécs, Hungary.
Rolland GyulaiDepartment of Dermatology, Venerology and Oncodermatology Clinical Center, University of Pécs, Pécs, Hungary.
Zsuzsanna LengyelDepartment of Dermatology, Venerology and Oncodermatology Clinical Center, University of Pécs, Pécs, Hungary.

Funding

Center for Research and Training in Skin Diseases and Leprosy, Tehran University of Medical Sciences, Tehran, Iran 1400-2-105-53366Thematic Excellence Program 2021 Health Sub-programme of the Ministry for Innovation and Technology in Hungary, within the framework of the EGA-10 project of the University of Pécs
6 · The paper itself

Abstract

backgroundThe introduction of immune checkpoint inhibitors (ICIs) opened a new era in cancer immunotherapy. In particular, PD-1 inhibitors have shown remarkable efficacy in various cancers, most notably melanoma. However, the widespread use of immune checkpoint inhibitors comes with the challenge of immune-related adverse events (irAEs), with cutaneous toxicities being the most prevalent.

methodsA retrospective, single-center study was carried out to investigate the cutaneous side effects in patients diagnosed with melanoma and treated with PD-1 inhibitors (pembrolizumab or nivolumab) at the Department of Dermatology, Venereology, and Oncodermatology, University of Pécs, Hungary. The study included patients with stage III or IV melanoma who received PD-1 inhibitor monotherapy, either for metastatic or adjuvant purposes, from August 2015 to May 2022.

resultsA cohort of 174 patients was examined, with 29% experiencing cutaneous adverse events (cAEs). The most prevalent cutaneous toxicities were vitiligo (n = 18; 27%), maculopapular rash (n = 14; 21%), pruritus (n = 14; 21%), xerostomia (n = 8; 12%), and lichenoid dermatitis (n = 4; 6%). Treatment primarily involved topical corticosteroids and emollients, with a few cases requiring systemic therapy. Notably, the occurrence of dermatologic adverse events was associated with improved progression-free survival (PFS) (p = 0.007) and overall survival (OS) (p = 0.026) compared to those without any skin toxicity (p < 0.0001), emphasizing their potential prognostic significance. Our data were not influenced by any well-known prognostic factors of melanoma.

conclusionOur study contributes to the growing body of evidence supporting the prognostic value of cutaneous adverse events in patients treated with PD-1 inhibitors. Optimizing treatment strategies while maintaining oncologic therapy is essential, highlighting the role of dermatologists in multidisciplinary cancer care.

Indexed as

Antibodies, Monoclonal, HumanizedDrug EruptionsImmune Checkpoint InhibitorsMelanomaNivolumabSkin NeoplasmsAdultAgedAged, 80 and overFemaleHumansLichenoid EruptionsMaleMiddle AgedProgrammed Cell Death 1 ReceptorPruritusAntibodies, Monoclonal, HumanizedImmune Checkpoint InhibitorsNivolumabPDCD1 protein, humanpembrolizumabProgrammed Cell Death 1 Receptorimmune checkpoint inhibitorsimmune‐related cutaneous side effectmelanomaPD‐1 inhibitorskin toxicity

Identifiers

PMID39925013
PMCPMC12082620

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Registered trials

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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.