Evidence map›Paper›PMID 41155159›Full record

ArticleInternational journal of molecular sciences2025

Targeted Inhibition in Pediatric MET and ALK-Altered Hemispheric Gliomas: Objective Responses Followed by Treatment Resistance.

David Wilson, Sateesh Jayappa, Lora Parker, Eylem Ocal, Tomoko Tanaka, Murat Gokden, Kevin Bielamowicz

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In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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3 · Its place in the literature

Who cites it

0 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

7 authors.

David WilsonDepartment of Pediatrics, University of Arkansas for Medical Sciences (UAMS), Little Rock, AR 72223, USA.ORCID 0000-0003-2648-5870
Sateesh JayappaArkansas Children's Hospital (ACH), Little Rock, AR 72223, USA.
Lora ParkerArkansas Children's Hospital (ACH), Little Rock, AR 72223, USA.
Eylem OcalArkansas Children's Hospital (ACH), Little Rock, AR 72223, USA.ORCID 0000-0001-6762-0106
Tomoko TanakaArkansas Children's Hospital (ACH), Little Rock, AR 72223, USA.
Murat GokdenDepartment of Pathology, University of Arkansas for Medical Sciences (UAMS), Little Rock, AR 72223, USA.
Kevin BielamowiczDepartment of Pediatrics, University of Arkansas for Medical Sciences (UAMS), Little Rock, AR 72223, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pediatric-type diffuse high-grade gliomas (pHGGs) tend to have a dismal prognosis. Some of these gliomas feature alterations in genes such as ROS1, ALK, MET, and NTRK1-3. Despite development of targeted agents, the therapeutic application of these agents in pHGGs is still unclear. The aim of this retrospective case series is to report the outcome of two patients with pHGGs who were treated at Arkansas Children's Hospital with targeted agents (Cabozantinib for a MET fusion in patient 1 and Lorlatinib for an ALK fusion in patient 2) with an initial, objective response followed by treatment resistance. Each diagnosis was determined based on histology, targeted tumor sequencing, and methylation profiling. In both cases, relapse occurred while on targeted inhibition. Recurrent tumor sequencing for patient 2 revealed a MET copy gain suggesting a mechanism of resistance in this patient. Pediatric high-grade gliomas with targetable alterations can show objective responses to pathway inhibition. Relapse after initial response may warrant additional surgical samples to identify new alterations which can lead to changes in therapy. Larger prospective cohorts are needed to study targeted agents in this population, and earlier integration of these agents may be beneficial.

Indexed as

Anaplastic Lymphoma KinaseBrain NeoplasmsDrug Resistance, NeoplasmGliomaProtein Kinase InhibitorsProto-Oncogene Proteins c-metAminopyridinesChild, PreschoolFemaleHumansInfantLactamsLactams, MacrocyclicMaleMolecular Targeted TherapyPyrazolesALK protein, humanAminopyridinesAnaplastic Lymphoma KinaseLactamsLactams, MacrocycliclorlatinibMET protein, humanProtein Kinase InhibitorsProto-Oncogene Proteins c-metPyrazolesALK alterationbrain tumorgliomaMET alterationpediatric CNS tumorpediatric high-grade glioma

Identifiers

PMID41155159
PMCPMC12563772

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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.