Evidence map›Paper›PMID 38772345›Full record

ArticleDermatology (Basel, Switzerland)2024

Cutaneous Reactions in Pediatric Patients Treated with MEK Inhibitors: A Retrospective Single-Center Study.

Rivka Friedland, Mirit Glick, Iris Amitay-Laish, Helen Toledano

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Article in Dermatology (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

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0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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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

4 authors.

Rivka FriedlandPediatric Dermatology Unit, Schneider Children's Medical Center, Petah Tiqva, Israel.
Mirit GlickPediatric Dermatology Unit, Schneider Children's Medical Center, Petah Tiqva, Israel.
Iris Amitay-LaishFaculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Helen ToledanoFaculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMitogen-activated extracellular signal-regulated kinase (MEK) inhibitors are in use for several indications for adults and children. Cutaneous toxicities are among the most common adverse effects. We aimed to describe the spectrum of cutaneous adverse events, its frequency, and severity in a cohort of pediatric patients.

methodsWe reviewed all records of patients in our tertiary treatment center treated with MEK inhibitors between January 2016 and January 2023 for all indications.

resultsAmong 33 patients, 76% reported cutaneous adverse effects. The highest prevalence was in the group of patients treated with trametinib (90%), followed by the group treated with selumetinib (50%) and the group treated with a combination of trametinib and B-Raf proto-oncogene serine/threonine-protein kinase inhibitor (dabrafenib, 34%). Xerosis, dermatitis, paronychia, and hair heterochromia were most frequently reported. Severity was graded 1 or 2 for most adverse events, and 237 visits to the dermatology clinic related to these adverse events were recorded.

conclusionsCutaneous adverse events are common in the pediatric population as in adults, but the clinical spectrum is different. Although considered mild, multiple dermatological consultations reflect the distress caused by these events. Dermatologists have a central role in the multidisciplinary care of pediatric patients receiving these agents.

Indexed as

Drug EruptionsProtein Kinase InhibitorsProto-Oncogene MasAdolescentBenzimidazolesChildChild, PreschoolFemaleHumansImidazolesInfantMaleOximesParonychiaPyridonesPyrimidinonesAZD 6244BenzimidazolesdabrafenibImidazolesMAS1 protein, humanOximesProtein Kinase InhibitorsProto-Oncogene MasPyridonesPyrimidinonestrametinibAdverse drug reactionChildMedical oncology

Identifiers

PMID38772345
PMCPMC11309057

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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.