Evidence map›Paper›PMID 38392562›Full record

ArticleJournal of personalized medicine2024

Clinical Impact of Comprehensive Molecular Profiling in Adolescents and Young Adults with Sarcoma.

Eden C Andrew, Jeremy Lewin, Jayesh Desai, Lisa Orme, Anne Hamilton, Susie Bae, Wenying Zhu, Shannon Nicolson, Leila N Varghese, Camilla B Mitchell and 5 more

Abstract read
In one paragraph

Article in Journal of personalized medicine, 2024. 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

15 authors.

Eden C AndrewDepartment of Medical Oncology, Peter MacCallum Cancer Centre, Parkville, VIC 3000, Australia.ORCID 0000-0002-2122-560X
Jeremy LewinDepartment of Medical Oncology, Peter MacCallum Cancer Centre, Parkville, VIC 3000, Australia.
Jayesh DesaiDepartment of Medical Oncology, Peter MacCallum Cancer Centre, Parkville, VIC 3000, Australia.
Lisa OrmeDepartment of Medical Oncology, Peter MacCallum Cancer Centre, Parkville, VIC 3000, Australia.
Anne HamiltonDepartment of Medical Oncology, Peter MacCallum Cancer Centre, Parkville, VIC 3000, Australia.
Susie BaeDepartment of Medical Oncology, Peter MacCallum Cancer Centre, Parkville, VIC 3000, Australia.
Wenying ZhuCentre for Cancer Research and Department of Clinical Pathology, The University of Melbourne, Melbourne, VIC 3010, Australia.
Shannon NicolsonCentre for Cancer Research and Department of Clinical Pathology, The University of Melbourne, Melbourne, VIC 3010, Australia.
Leila N VargheseCentre for Cancer Research and Department of Clinical Pathology, The University of Melbourne, Melbourne, VIC 3010, Australia.
Camilla B MitchellCentre for Cancer Research and Department of Clinical Pathology, The University of Melbourne, Melbourne, VIC 3010, Australia.
Joseph H A VissersCentre for Cancer Research and Department of Clinical Pathology, The University of Melbourne, Melbourne, VIC 3010, Australia.ORCID 0000-0003-0435-6824
Huiling XuDepartment of Pathology and Cancer Research Division, Peter MacCallum Cancer Centre, Parkville, VIC 3000, Australia.
Sean M GrimmondCentre for Cancer Research and Department of Clinical Pathology, The University of Melbourne, Melbourne, VIC 3010, Australia.
Stephen B FoxSir Peter MacCallum Department of Oncology, The University of Melbourne, Melbourne, VIC 3010, Australia.ORCID 0000-0002-7648-8896
Stephen J LuenDepartment of Medical Oncology, Peter MacCallum Cancer Centre, Parkville, VIC 3000, Australia.

Funding

Victorian Comprehensive Cancer Centre Not applicable
6 · The paper itself

Abstract

Sarcomas are a heterogenous group of tumours that commonly carry poor prognosis with limited therapeutic options. Adolescents and young adults (AYAs) with sarcoma are a unique and understudied patient population that have only achieved modest survival gains compared to other groups. We present our institutional experience of AYAs with sarcoma who underwent comprehensive molecular profiling (CMP) via either large-panel targeted DNA sequencing or whole genome and transcriptome sequencing and evaluated the feasibility and clinical impact of this approach. Genomic variants detected were determined to be clinically relevant and actionable following evaluation by the Molecular Tumour Board. Clinicians provided feedback regarding the utility of testing three months after reporting. Twenty-five patients who were recruited for CMP are included in this analysis. The median time from consent to final molecular report was 45 days (interquartile range: 37-57). Potentially actionable variants were detected for 14 patients (56%), and new treatment recommendations were identified for 12 patients (48%). Pathogenic germline variants were identified in three patients (12%), and one patient had a change in diagnosis. The implementation of CMP for AYAs with sarcoma is clinically valuable, feasible, and should be increasingly integrated into routine clinical practice as technologies and turnaround times continue to improve.

Indexed as

adolescents and young adults (AYAs) with cancerdiagnostic biomarkersgenomicsmolecular profilingnext-generation sequencingprecision oncologysarcomawhole genome sequencing

Identifiers

PMID38392562
PMCPMC10890624

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.