Evidence map›Paper›PMID 42652943›Full record

ArticleLife (Basel, Switzerland)2026

Cutaneous Graft-Versus-Host Disease After Allogeneic Hematopoietic Stem Cell Transplantation: A Single-Center Retrospective Cohort Study of Clinical Spectrum and Treatment Patterns.

Annunziata Raimondo, Annunziata Nigro, Mara Corbisieri, Valentina Giudice, Bianca Serio, Serena Lembo, Carmine Selleri

Abstract read
In one paragraph

Article in Life (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Annunziata RaimondoDepartment of Medicine Surgery and Dentistry, "Scuola Medica Salernitana", University of Salerno, 84084 Salerno, Italy.ORCID 0000-0002-0849-715X
Annunziata NigroDepartment of Medicine Surgery and Dentistry, "Scuola Medica Salernitana", University of Salerno, 84084 Salerno, Italy.ORCID 0000-0002-1838-1484
Mara CorbisieriDepartment of Medicine Surgery and Dentistry, "Scuola Medica Salernitana", University of Salerno, 84084 Salerno, Italy.
Valentina GiudiceDepartment of Medicine Surgery and Dentistry, "Scuola Medica Salernitana", University of Salerno, 84084 Salerno, Italy.ORCID 0000-0002-7492-6848
Bianca SerioHematology and Transplant Center, University Hospital "San Giovanni Di Dio E Ruggi d'Aragona", 84131 Salerno, Italy.
Serena LemboDepartment of Medicine Surgery and Dentistry, "Scuola Medica Salernitana", University of Salerno, 84084 Salerno, Italy.
Carmine SelleriDepartment of Medicine Surgery and Dentistry, "Scuola Medica Salernitana", University of Salerno, 84084 Salerno, Italy.ORCID 0000-0002-5861-8984

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cutaneous graft-versus-host disease (GVHD) is a common complication of allogeneic haematopoietic stem cell transplantation (allo-HSCT). Despite established guidelines, discrepancies persist between clinical trial evidence and real-world practice, particularly for newer agents such as ruxolitinib. To characterize the phenotypic spectrum of cutaneous GVHD, evaluate real-world treatment strategies-with a specific focus on systemic and topical ruxolitinib-and assess adherence to national and international guidelines, we conducted a retrospective observational study of patients undergoing allo-HSCT between 2015 and 2025 who were referred to a dedicated dermato-haematology clinic. Clinical, histological, and therapeutic data were collected. Cutaneous manifestations were classified according to National Institutes of Health (NIH) and Italian Group for Blood and Marrow Transplantation (GITMO) criteria. Of 62 transplanted patients, 44 (71%) developed GVHD, with the skin as the most frequently involved organ. Acute GVHD predominantly presented with maculopapular eruptions, whereas chronic GVHD showed heterogeneous phenotypes, including sclerotic variants. First-line management was largely guideline-concordant. Systemic ruxolitinib was administered to 3% of patients in the aGVHD group and 3% in the cGVHD group. Steroid-refractory and steroid-dependent status was not systematically recorded; therefore, treatment eligibility could not be reliably determined, and the observed frequencies should not be interpreted as evidence of underuse. Topical ruxolitinib was not used and remains investigational for cutaneous GVHD. Interpretation should also consider that the study period encompassed changes in regulatory approval, reimbursement, and access to targeted therapies. Structured multidisciplinary assessment may support the management of complex cutaneous GVHD, although its effects on treatment decisions and patient outcomes require prospective evaluation.

Indexed as

allogeneic stem cell transplantationcutaneous graft-versus-host diseasereal-world evidenceruxolitinibsteroid-refractory GVHD

Identifiers

PMID42652943
PMCPMC13514361

What Socratic holds

Textmetadata
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 Socratic graph.