Evidence map›Paper›PMID 40117481›Full record

ArticleMagyar onkologia2025

[First results of comprehensive genomic studies on solid tumours in National Institute of Oncology].

Erika Tóth, Erzsébet Csernák, Andrea Kohánka, László Báthory-Fülöp, Henriett Butz, Attila Patócs, Tamás Pintér, Zsolt Horváth, Zsófia Küronya, Tamás Strausz and 2 more

Abstract readEnglish Abstract
In one paragraph

Article in Magyar onkologia, 2025. 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

12 authors.

Erika TóthSebészeti és Molekuláris Patológiai Osztály, Országos Onkológiai Intézet, Budapest, Hungary. dr.toth.erika@oncol.hu.
Erzsébet CsernákSebészeti és Molekuláris Patológiai Osztály, Országos Onkológiai Intézet, Budapest, Hungary. dr.toth.erika@oncol.hu.
Andrea KohánkaSebészeti és Molekuláris Patológiai Osztály, Országos Onkológiai Intézet, Budapest, Hungary. dr.toth.erika@oncol.hu.
László Báthory-FülöpSebészeti és Molekuláris Patológiai Osztály, Országos Onkológiai Intézet, Budapest, Hungary. dr.toth.erika@oncol.hu.
Henriett ButzMolekuláris Genetikai Osztály, Országos Onkológiai Intézet, Budapest, Hungary.
Attila PatócsMolekuláris Genetikai Osztály, Országos Onkológiai Intézet, Budapest, Hungary.
Tamás PintérMellkasi és Hasüregi Daganatok és Klinikai Farmakológiai Osztály "Kemoterápia B", Országos Onkológiai Intézet, Budapest, Hungary.
Zsolt HorváthMellkasi és Hasüregi Daganatok és Klinikai Farmakológiai Osztály "Kemoterápia B", Országos Onkológiai Intézet, Budapest, Hungary.
Zsófia KüronyaUrogenitális Tumorok és Klinikai Farmakológiai Osztály "Kemoterápia C", Országos Onkológiai Intézet, Budapest, Hungary.
Tamás StrauszSebészeti és Molekuláris Patológiai Osztály, Országos Onkológiai Intézet, Budapest, Hungary. dr.toth.erika@oncol.hu.
Imola AdamikSebészeti és Molekuláris Patológiai Osztály, Országos Onkológiai Intézet, Budapest, Hungary. dr.toth.erika@oncol.hu.
Zsombor MeleghSebészeti és Molekuláris Patológiai Osztály, Országos Onkológiai Intézet, Budapest, Hungary. dr.toth.erika@oncol.hu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsThe Molecular Pathology Laboratory of the National Institute of Oncology has been performing comprehensive genomic studies (500-gene panel) since 2021. This paper summarizes our results obtained between 2022 and 2024, focusing on clinical requests, the histological type of cases studied and the potential therapeutic benefit of identified variants.

methodsComprehensive genomic profiling was performed using next generation sequencing on an Ion S5 Plus system (Thermo Fisher Scientific) with Oncomine Comprehensive Assay Plus kit. DNA and RNA were extracted from formalin- fixed, paraffin-embedded samples.

results402 analyses were performed. We identified mutations with therapeutic significance in 37.3% (150/402) of cases, including 26.4% (106/402) of cases with on label therapies. The most frequently investigated cases were soft tissue sarcomas and gynaecological tumours.

conclusionsGenetic alterations with therapeutic relevance primarily include high TMB and high GIS. Previously unknown mutations suitable for targeted therapy were rarely identified, as almost all cases had previously undergone small targeted panel testing.

Indexed as

GenomicsNeoplasmsAdultBiomarkers, TumorFemaleGenital Neoplasms, FemaleHigh-Throughput Nucleotide SequencingHumansMaleMiddle AgedMolecular Targeted TherapyMutationSarcomaBiomarkers, Tumor

Identifiers

PMID40117481
PMCPMC11929570

What OpenQuestion holds

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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.