Evidence map›Paper›PMID 39887903›Full record

ArticleMolecular oncology2025

Analysis of comprehensive genomic profiling of solid tumors with a novel assay for broad analysis in clinical diagnostics.

Guy Froyen, Pieter-Jan Volders, Ellen Geerdens, Severine Berden, Joni Van der Meulen, Aaron De Cock, Stefanie Vermeire, Jacques Van Huysse, Marie de Barsy, Gabriela Beniuga and 8 more

Abstract readComparative StudyMulticenter Study
In one paragraph

Article in Molecular oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

18 authors.

Guy FroyenLaboratory for Molecular Diagnostics, Department of Clinical Biology, Jessa Hospital, Hasselt, Belgium.ORCID https://orcid.org/0000-0002-6671-1572
Pieter-Jan VoldersLaboratory for Molecular Diagnostics, Department of Clinical Biology, Jessa Hospital, Hasselt, Belgium.ORCID https://orcid.org/0000-0002-2685-2637
Ellen GeerdensLaboratory for Molecular Diagnostics, Department of Clinical Biology, Jessa Hospital, Hasselt, Belgium.
Severine BerdenLaboratory for Molecular Diagnostics, Department of Clinical Biology, Jessa Hospital, Hasselt, Belgium.
Joni Van der MeulenDepartment of Biomolecular Medicine, Ghent University, Ghent, Belgium.ORCID https://orcid.org/0000-0002-1916-2769
Aaron De CockMolecular Diagnostics Ghent University Hospital (MDG), Ghent University Hospital, Ghent, Belgium.ORCID https://orcid.org/0009-0009-5246-2761
Stefanie VermeireDepartment of Pathology, AZ Sint-Jan Brugge AV, Bruges, Belgium.
Jacques Van HuysseDepartment of Pathology, AZ Sint-Jan Brugge AV, Bruges, Belgium.
Marie de BarsyInstitute of Pathology and Genetics (IPG), Gosselies, Belgium.
Gabriela BeniugaInstitute of Pathology and Genetics (IPG), Gosselies, Belgium.
Wendy W J de LengDepartment of Pathology, University Medical Centre Utrecht, The Netherlands.ORCID https://orcid.org/0000-0003-2911-6018
Anne M L JansenDepartment of Pathology, University Medical Centre Utrecht, The Netherlands.
Imke DemersDepartment of Pathology, Maastricht University Medical Center, Maastricht, The Netherlands.
Zeliha OzgurGenomics Core Facility, Erasmus University Medical Center, Rotterdam, The Netherlands.
Hendrikus Jan DubbinkDepartment of Pathology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.ORCID https://orcid.org/0000-0002-2160-5207
Ernst-Jan M SpeelDepartment of Pathology, Maastricht University Medical Center, Maastricht, The Netherlands.ORCID https://orcid.org/0000-0002-3016-2989
Wilfred F J van IJckenGenomics Core Facility, Erasmus University Medical Center, Rotterdam, The Netherlands.ORCID https://orcid.org/0000-0002-0421-8301
Brigitte MaesLaboratory for Molecular Diagnostics, Department of Clinical Biology, Jessa Hospital, Hasselt, Belgium.ORCID https://orcid.org/0009-0004-2301-3370

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Somatic multigene analysis by next-generation sequencing (NGS) is routinely integrated in medical oncology for clinical decision-making. However, with the fast-growing number of recommended and required genes as well as pan-cancer biomarkers, small panels have become vastly insufficient. Comprehensive genomic profiling (CGP) is, thus, required to screen for clinically relevant markers. In this multicentric study, we report on an extensive analysis across seven centers comparing the results of the novel OncoDEEP CGP assay with the diagnostically validated TruSight Oncology 500 (TSO500) kit on 250 samples. Overall concordance was 90% for clinically relevant gene variants and >96% for more complex biomarkers. Agreement for fusion detection was 94% for the 11 overlapping clinically actionable driver genes. The higher coverage uniformity of OncoDEEP compared to TSO500 allows users to pool more samples per sequencing run. Tertiary data analysis, including reporting, is integrated in the OncoDEEP solution, whereas this is an add-on for TSO500. Finally, we showed that, analytically, the OncoDEEP panel performs well, thereby advocating its use for CGP of solid tumors in diagnostic laboratories, providing an all-in-one solution for optimal patient management.

Indexed as

Gene Expression ProfilingGenomicsNeoplasmsBiomarkers, TumorFemaleHigh-Throughput Nucleotide SequencingHumansMaleBiomarkers, Tumorcomprehensive genomic profiling (CGP)diagnostic assay validationnext‐generation sequencing (NGS)solid tumors

Identifiers

PMID39887903
PMCPMC12161465

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.