Evidence map›Paper›PMID 40425247›Full record

ArticleBMJ open2025

Does paired genetic testing improve targeted therapy choices and screening recommendations for patients with upper gastrointestinal cancers and their families? A prospective cohort of 42 patients.

Kevin Tatunay, Stacey Cohen, Lorraine V Naylor, Cynthia L Handford, Angela Jacobson, Veena Shankaran, Brant Oelschlager, William M Grady, Britta Sjoding, Everett Lally and 6 more

Abstract read
In one paragraph

Article in BMJ open, 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

16 authors.

Kevin TatunayFred Hutchinson Cancer Center, Seattle, Washington, USA.
Stacey CohenFred Hutchinson Cancer Center, Seattle, Washington, USA.ORCID http://orcid.org/0000-0002-6207-9856
Lorraine V NaylorFred Hutchinson Cancer Center, Seattle, Washington, USA.
Cynthia L HandfordFred Hutchinson Cancer Center, Seattle, Washington, USA.
Angela JacobsonUniversity of Washington, Seattle, Washington, USA.
Veena ShankaranFred Hutchinson Cancer Center, Seattle, Washington, USA.
Brant OelschlagerUniversity of Washington, Seattle, Washington, USA.
William M GradyFred Hutchinson Cancer Center, Seattle, Washington, USA.
Britta SjodingFred Hutchinson Cancer Center, Seattle, Washington, USA.
Everett LallyFred Hutchinson Cancer Center, Seattle, Washington, USA.
Lauren FacchiniFred Hutchinson Cancer Center, Seattle, Washington, USA.
Qin SunFred Hutchinson Cancer Center, Seattle, Washington, USA.
Mercy Y LaurinoFred Hutchinson Cancer Center, Seattle, Washington, USA.
Colin PritchardUniversity of Washington, Seattle, Washington, USA.
Eric Q KonnickUniversity of Washington, Seattle, Washington, USA.
Marianne E Dubard-GaultFred Hutchinson Cancer Center, Seattle, Washington, USA Marianne.Dubard-Gault@Swedish.org.ORCID http://orcid.org/0000-0002-5735-1819

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesOur study was designed to assess whether paired normal-tumour testing increased access to targeted therapy, clinical trials and influenced cancer screening recommendations given to patients and their families.

designProspective cohort study.

settingAcademic cancer centre in the Pacific Northwest region of the USA.

participantsPatients newly diagnosed between 01 January 2021 and 31 December 2022 with cancers of the oesophagus, gastro-oesophageal junction and stomach (CEGEJS) were included. All other cancer diagnoses such as head and neck, duodenal and lower gastrointestinal tract cancers were excluded.

interventionPaired germline and tumour genetic test within 90 days of new patient visit. PRIMARY OUTCOME MEASURES: Number of targeted therapies received (or not) when eligible, follow-up treatment data and number of inherited predispositions to cancers identified. No secondary outcome measures.

resultsOf 42 patients, 32 (76.2%) were eligible for at least one targeted therapy. 19 patients received immunotherapy, when 16 had a biomarker predicting immunotherapy benefit, and benefit of immunotherapy was unclear for 3. Another 11 did not have this biomarker, and 6 of them received immunotherapy. Six pathogenic variants were identified in four high-risk genes. By 01 January 2024, 18 patients (42.9%) had died of complications of cancer.

conclusionMore than 75% of patients who received tumour testing were eligible for a targeted therapy regardless of their stage at diagnosis, emphasising the need to expand access to testing with staging workup to improve survival outcomes. Six families received personalised screening recommendations, thanks to this study.

Indexed as

Early Detection of CancerEsophageal NeoplasmsGastrointestinal NeoplasmsGenetic TestingMolecular Targeted TherapyStomach NeoplasmsAdultAgedFemaleGenetic Predisposition to DiseaseHumansMaleMiddle AgedProspective StudiesCancer geneticsCHEMOTHERAPYGastrointestinal tumoursHealth ServicesMolecular aspects

Identifiers

PMID40425247
PMCPMC12107587

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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.