Evidence map›Paper›PMID 41217720›Full record

ArticleMolecular diagnosis & therapy2026

Clinical Utility of an RNA-based Gene Fusion Assay in Sarcoma for Diagnosis and Management: Experience in an Australian Laboratory.

Adel Shahnam, Catherine Mitchell, Christopher R McEvoy, Owen W J Prall, Huiling Xu, Andrew P Fellowes, David Y Choong, Christopher M Angel, Christine Khoo, Jia-Min Pang and 8 more

Abstract read
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Article in Molecular diagnosis & therapy, 2026. 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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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

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5 · Who and what money

Authors and funding

18 authors.

Adel Shahnam *Department of Cancer Medicine, Peter MacCallum Cancer Centre, Melbourne, VIC, 3000, Australia.
Catherine Mitchell *Department of Pathology, Peter MacCallum Cancer Centre, 305 Grattan St, Melbourne, Victoria, 3000, Australia. Catherine.Mitchell@petermac.org.ORCID 0000-0001-5596-9511
Christopher R McEvoyDepartment of Pathology, Peter MacCallum Cancer Centre, 305 Grattan St, Melbourne, Victoria, 3000, Australia.
Owen W J PrallDepartment of Pathology, Peter MacCallum Cancer Centre, 305 Grattan St, Melbourne, Victoria, 3000, Australia.
Huiling XuDepartment of Pathology, Peter MacCallum Cancer Centre, 305 Grattan St, Melbourne, Victoria, 3000, Australia.
Andrew P FellowesDepartment of Pathology, Peter MacCallum Cancer Centre, 305 Grattan St, Melbourne, Victoria, 3000, Australia.
David Y ChoongDepartment of Pathology, Peter MacCallum Cancer Centre, 305 Grattan St, Melbourne, Victoria, 3000, Australia.
Christopher M AngelDepartment of Pathology, Peter MacCallum Cancer Centre, 305 Grattan St, Melbourne, Victoria, 3000, Australia.
Christine KhooDepartment of Pathology, Peter MacCallum Cancer Centre, 305 Grattan St, Melbourne, Victoria, 3000, Australia.
Jia-Min PangDepartment of Pathology, Peter MacCallum Cancer Centre, 305 Grattan St, Melbourne, Victoria, 3000, Australia.
Cameron SnellDepartment of Pathology, Peter MacCallum Cancer Centre, 305 Grattan St, Melbourne, Victoria, 3000, Australia.
Chris Van VlietDepartment of Pathology, Peter MacCallum Cancer Centre, 305 Grattan St, Melbourne, Victoria, 3000, Australia.
Stephen J LuenDepartment of Cancer Medicine, Peter MacCallum Cancer Centre, Melbourne, VIC, 3000, Australia.
Susie BaeDepartment of Cancer Medicine, Peter MacCallum Cancer Centre, Melbourne, VIC, 3000, Australia.
Anne HamiltonDepartment of Cancer Medicine, Peter MacCallum Cancer Centre, Melbourne, VIC, 3000, Australia.
Jayesh DesaiDepartment of Cancer Medicine, Peter MacCallum Cancer Centre, Melbourne, VIC, 3000, Australia.
Stephen B FoxDepartment of Pathology, Peter MacCallum Cancer Centre, 305 Grattan St, Melbourne, Victoria, 3000, Australia.
Jeremy LewinDepartment of Cancer Medicine, Peter MacCallum Cancer Centre, Melbourne, VIC, 3000, Australia.

Funding

Peter MacCallum Foundation 2019 Foundation Grant #1937
6 · The paper itself

Abstract

backgroundSarcoma represents a diverse group of over 70 subtypes with overlapping morphological and immunophenotypic features, often leading to diagnostic uncertainty. Gene fusions are commonly associated with specific sarcoma subtypes and can aid in diagnosis and management. RNA-based next-generation sequencing (NGS) enables sensitive detection of gene fusions, particularly in cases with limited tissue or ambiguous histopathology.

methodsWe conducted a retrospective review of 124 patients with suspected sarcoma who underwent RNA-based NGS using the Illumina TruSight RNA Fusion Panel (TRFP) at a dedicated sarcoma centre between June 2020 and June 2023. The impact of fusion testing on diagnostic classification and treatment decisions was evaluated by expert pathologists and oncologists.

resultsGene fusions were detected in 75 of 124 cases (60%). Fusion results confirmed the initial diagnosis in 58 cases (47%) and altered the diagnosis in 17 cases (14%). In 14 cases (11%), findings directly influenced clinical management, including treatment de-escalation (nine cases) and initiation of targeted or alternative therapies (five cases). A definitive diagnosis was achieved in 59% of cases with limited tissue (41 of 70), 48% with uncertain tumour differentiation (25 of 52), and 43% with inconclusive or failed prior molecular testing (ten of 23), underscoring the utility of RNA-based NGS in diagnostically complex scenarios.

conclusionsRNA-based NGS fusion panels provide diagnostic and clinical utility in the evaluation of mesenchymal tumours. Their integration into routine diagnostic workflows improves diagnostic accuracy and informs personalised treatment decisions, especially in diagnostically complex or resource-limited settings.

Indexed as

Gene FusionOncogene Proteins, FusionSarcomaAdolescentAdultAgedAged, 80 and overAustraliaBiomarkers, TumorDisease ManagementFemaleHigh-Throughput Nucleotide SequencingHumansMaleMiddle AgedRetrospective StudiesBiomarkers, TumorOncogene Proteins, Fusion

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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.