Evidence map›Paper›PMID 40144205›Full record

ArticlePathology oncology research : POR2025

Impact of comprehensive genomic profiling on the diagnosis and clinical management of malignant mesenchymal tumours.

Anna Beáta Csepregi, Eszter Papp, Imola Adamik, Erzsébet Csernák, Helga Engi, Zsófia Küronya, Edina Soós, Zsombor Melegh, Erika Tóth

Abstract read
In one paragraph

Article in Pathology oncology research : POR, 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

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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

The trial behind it

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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.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

9 authors.

Anna Beáta CsepregiDepartment of Surgical and Molecular Pathology, Centre of Tumour Pathology, National Institute of Oncology, Budapest, Hungary.
Eszter PappDepartment of Surgical and Molecular Pathology, Centre of Tumour Pathology, National Institute of Oncology, Budapest, Hungary.
Imola AdamikDepartment of Surgical and Molecular Pathology, Centre of Tumour Pathology, National Institute of Oncology, Budapest, Hungary.
Erzsébet CsernákDepartment of Surgical and Molecular Pathology, Centre of Tumour Pathology, National Institute of Oncology, Budapest, Hungary.
Helga EngiDepartment of Surgical and Molecular Pathology, Centre of Tumour Pathology, National Institute of Oncology, Budapest, Hungary.
Zsófia KüronyaDepartment of Urogenital Tumours and Clinical Pharmacology, National Institute of Oncology, Budapest, Hungary.
Edina SoósDepartment of Urogenital Tumours and Clinical Pharmacology, National Institute of Oncology, Budapest, Hungary.
Zsombor MeleghDepartment of Surgical and Molecular Pathology, Centre of Tumour Pathology, National Institute of Oncology, Budapest, Hungary.
Erika TóthDepartment of Surgical and Molecular Pathology, Centre of Tumour Pathology, National Institute of Oncology, Budapest, Hungary.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Comprehensive genomic profiling (CGP) is becoming an increasingly important tool in the clinical management of different tumours, but there is still very limited data available on its usefulness from a therapeutic point of view in mesenchymal tumours. Between January 2022 and September 2024, we performed CGP analysis with means of Oncomine Comprehensive Assay Plus (OCAplus) on 94 malignant mesenchymal tumours. The analysis covered more than 500 unique genes for single-gene and multigene biomarker insights, including tumour mutational burden (TMB) and homologous recombination deficiency (HRD). Genomic DNA and total RNA were extracted from formalin-fixed paraffin-embedded tissue blocks. Twenty-four out of 94 patients (25.5%) had potentially actionable alterations: 17 (18%) had specific genetic alterations suitable for targeted therapies, 4 (4.2%) had a high TMB (>10 mut/Mb), and 5 (5.3%) had a high HRD score >15). One additional patient had

Indexed as

Biomarkers, TumorGene Expression ProfilingAdultAgedAged, 80 and overFemaleGenomicsHumansMaleMiddle AgedMutationPrognosisYoung AdultBiomarkers, Tumorcomprehensive genomic profilingmesenchymal tumoursnext generation sequencingsarcomatargeted therapy

Identifiers

PMID40144205
PMCPMC11936746

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Registered trials

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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.