Evidence map›Paper›PMID 40052589›Full record

ReviewJournal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG2025

Immune checkpoint inhibitors for children with xeroderma pigmentosum and advanced cutaneous squamous cell carcinoma: A case presentation and brief review.

Thilo Gambichler, Julia Hyun, Frank Oellig, Jürgen C Becker, Alexander Kreuter

Abstract readCase ReportsReview
In one paragraph

Review in Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–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

2 citing papers in PubMed.

  1. Review
  2. Immune checkpoint inhibitors for children with xeroderma pigmentosum and advanced cutaneous squamous cell carcinoma: A case presentation and brief review.Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG · 2025
    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

5 authors.

Thilo GambichlerDepartment of Dermatology, Dortmund Hospital, University Witten-Herdecke, Faculty of Health/School of Medicine, Dortmund, Germany.
Julia HyunDepartment of Dermatology, Venereology, and Allergology, Helios St. Johannes Hospital Duisburg, Duisburg, Germany.
Frank OelligDepartment of Pathology, Mülheim an der Ruhr, Germany.
Jürgen C BeckerTranslational Skin Cancer Research, DKTK Partner Site Essen/Düsseldorf, Germany.
Alexander KreuterDepartment of Dermatology, Venereology, and Allergology, Helios St. Johannes Hospital Duisburg, Duisburg, Germany.ORCID 0000-0003-2275-499X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients with xeroderma pigmentosum (XP) frequently develop skin cancers early in life, including cutaneous squamous cell carcinoma (cSCC). The median age of death is 32 years and 60% of XP patients die before the age of 20 years. cSCC in patients with XP exhibits an exceptionally high mutation burden, suggesting a favorable response to immune checkpoint inhibitors (ICIs). We present the case of a 7-year-old boy with XP and a large facial cSCC complicated by cervical lymph node metastases. Following a tumor board recommendation, systemic immunotherapy with cemiplimab was initiated. Following therapy, the tumors rapidly and completely regressed. To date, only 10 XP patients worldwide have been reported to receive ICIs for inoperable and/or advanced cSCC, with all cases demonstrating tumor regression under ICI treatment. Among these, three were pediatric cases with XP-C (one 7-year-old and two 6-year-old children), one of whom had sarcomatoid cSCC. Incidence and nature of adverse events in XP patients were comparable to those observed in the general population. In line with the previously reported ICI-treated XP children, the present case confirms that anti-PD-1 inhibitors are highly effective in children with XP and advanced cSCC.

Indexed as

Antibodies, Monoclonal, HumanizedCarcinoma, Squamous CellImmune Checkpoint InhibitorsSkin NeoplasmsXeroderma PigmentosumChildHumansLymphatic MetastasisMaleAntibodies, Monoclonal, HumanizedcemiplimabImmune Checkpoint InhibitorscemiplimabchildhoodDNA repair defectsgenodermatosesgeno‐photodermatoseskeratoacanthomanivolumabpembrolizumab

Identifiers

PMID40052589
PMCPMC11886998

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.