Evidence map›Paper›PMID 41973363›Full record

ReviewMolecular and cellular pediatrics2026

Efficacy of azacitidine and trametinib against leptomeningeal melanosis associated with congenital melanocytic nevus syndrome.

Lina Raljević, Katalin Komlosi, Ursula Feige, Matthias Eckenweiler, Silke Lassmann, Haroun Bel Hadj Jrad, Martin Werner, Judith Fischer, Cristina Has, Tobias Feuchtinger and 3 more

Abstract readReview
In one paragraph

Review in Molecular and cellular pediatrics, 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

13 authors.

Lina RaljevićDivision of Pediatric Hematology and Oncology, Department of Pediatric and Adolescent Medicine, University Medical Center Freiburg, University of Freiburg, Freiburg, Germany.
Katalin KomlosiInstitute of Human Genetics, University Medical Center Freiburg, University of Freiburg, Freiburg, Germany.
Ursula FeigeDepartment of Neuroradiology, University Medical Center Freiburg, University of Freiburg, Freiburg, Germany.
Matthias EckenweilerDivision of Neuropediatrics and Muscular Diseases, Department of Pediatric and Adolescent Medicine, University Medical Center Freiburg, University of Freiburg, Freiburg, Germany.
Silke LassmannInstitute of Clinical Pathology, University Medical Center Freiburg, University of Freiburg, Freiburg, Germany.
Haroun Bel Hadj JradDepartment of Neuroradiology, University Medical Center Freiburg, University of Freiburg, Freiburg, Germany.
Martin WernerInstitute of Clinical Pathology, University Medical Center Freiburg, University of Freiburg, Freiburg, Germany.
Judith FischerInstitute of Human Genetics, University Medical Center Freiburg, University of Freiburg, Freiburg, Germany.
Cristina HasDepartment of Dermatology and Venerology, University Medical Center Freiburg, University of Freiburg, Freiburg, Germany.
Tobias FeuchtingerDivision of Pediatric Hematology and Oncology, Department of Pediatric and Adolescent Medicine, University Medical Center Freiburg, University of Freiburg, Freiburg, Germany.
Markus UhlDepartment of Radiology, Pediatric Radiology, and Interventional Radiology, St. Josefskrankenhaus, Sautierstraße 1, Freiburg, 79104, Germany.
Charlotte M NiemeyerDivision of Pediatric Hematology and Oncology, Department of Pediatric and Adolescent Medicine, University Medical Center Freiburg, University of Freiburg, Freiburg, Germany.
Simone HettmerDivision of Pediatric Hematology and Oncology, Department of Pediatric and Adolescent Medicine, University Medical Center Freiburg, University of Freiburg, Freiburg, Germany. simone.hettmer@uk-halle.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCongenital melanocytic nevus syndrome is a disorder characterized by postzygotic, mosaic NRAS Proto-Oncogene, GTPase mutations. Clinical manifestations include melanotic skin lesions and, optionally, central nervous system melanosis typically noted during early infancy. Affected individuals have an increased risk of developing malignant melanomas at an early age. CASE: We report a child with neurocutaneous melanosis due to this syndrome, who had innumerable nevi at birth and diffuse leptomeningeal thickening. He developed increased intracranial pressure at 4 weeks of age. The nucleoside analogue azacitidine and the Mitogen-Activated Protein Kinase, Kinase inhibitor trametinib were started at 6 weeks of age resulting in rapid reduction of leptomeningeal thickening. At 53 months of age, the patient still takes trametinib and has met all developmental milestones. There has been no evidence of melanoma, and he exhibits minimal residual leptomeningeal changes.

conclusionTo our best knowledge, this is the first child with this syndrome who has undergone successful therapy to reduce leptomeningeal thickening.

Identifiers

PMID41973363
PMCPMC13076836

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.