Evidence map›Paper›PMID 35258993›Full record

ArticleJCO oncology practice2022

Integrating Medical Genetics Into Precision Oncology Practice in the Veterans Health Administration: The Time Is Now.

Anthony Scott, Arathi Mohan, Sarah Austin, Erika Amini, Shelby Raupp, Brittany Pannecouk, Michael J Kelley, Goutham Narla, Nithya Ramnath

Open access · bronzeAbstract read
In one paragraph

Article in JCO oncology practice, 2022. 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
0.2field-weighted citation impact, top 41% of its field
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, 1 citations in OpenAlex.

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

9 authors at 3 institutions in 1 country.

Anthony ScottDivision of Genetic Medicine, Department of Internal Medicine, University of Michigan, Ann Arbor, MI.ORCID 0000-0003-0644-1790
Arathi MohanDivision of Oncology, Veterans Affairs Ann Arbor Healthcare System, Ann Arbor, MI.ORCID 0000-0001-9024-6589
Sarah AustinDivision of Genetic Medicine, Department of Internal Medicine, University of Michigan, Ann Arbor, MI.ORCID 0000-0003-4484-9746
Erika AminiDivision of Genetic Medicine, Department of Internal Medicine, University of Michigan, Ann Arbor, MI.ORCID 0000-0002-5952-0962
Shelby RauppDivision of Oncology, Veterans Affairs Ann Arbor Healthcare System, Ann Arbor, MI.ORCID 0000-0003-0282-7063
Brittany PannecoukDivision of Oncology, Veterans Affairs Ann Arbor Healthcare System, Ann Arbor, MI.
Michael J KelleyDivision of Hematology Oncology, Department of Medicine, Duke University, VA Medical Center in Durham, Durham, NC.ORCID 0000-0001-9523-6080
Goutham NarlaDivision of Genetic Medicine, Department of Internal Medicine, University of Michigan, Ann Arbor, MI.
Nithya RamnathDivision of Oncology, Veterans Affairs Ann Arbor Healthcare System, Ann Arbor, MI.
University of Michigan · USVA Ann Arbor Healthcare System · USDuke Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeIncreased access and utilization of tumor profiling of cancers in our veteran population uncovered a modest number of potentially pathogenic germline variants (PPGVs) that require genetics referral for follow-up evaluation and germline sequencing. Challenges identified specific to the veteran population include paucity of genetics providers, either at a veteran's VA facility or nearby non-VA facilities. We sought to investigate the number of veterans who would benefit from having such resources at both local and national levels.

methodsAnnotated clinical reports of mutations identified by tumor-only profiling and medical records of veterans with solid tumors at the Veterans Administration Ann Arbor Healthcare System (VA AAHS) between 2015 and 2020 were reviewed. PPGVs were identified according to society recommendations (such as ESMO and American Board of Medical Genetics and Genomics), expert review, and/or previously published criteria. After the analysis of our local VA population, these same criteria were then applied to veterans in the National Precision Oncology Program (NPOP).

resultsTwo hundred eight veterans underwent tumor profiling at the VA AAHS over the defined time period. This included 20 different primary tumor sites with over half (n = 130) being advanced cancer at diagnosis. Of these, 18 veterans (8.5%) had mutations suggestive of a PPGV. Applying these criteria to the larger NPOP database (n = 20,014), a similar percentage (6%) of PPGVs were identified.

conclusionThese results indicate a PPGV frequency (6%-9% of veterans) consistent with the prevalence of inherited cancer predisposition syndromes in the general population, underscoring the need for medical genetics as part of standard oncologic care for veterans. We explore current and future care delivery models to optimize incorporation of medical genetics and genetic counseling to best serve veterans needing such services.

Indexed as

Genetics, MedicalNeoplasmsHumansPrecision MedicineUnited StatesUnited States Department of Veterans AffairsVeterans Health

Identifiers

PMID35258993
PMCPMC9191304
OpenAlexW4220789060

What OpenQuestion holds

Textmetadata
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.