Evidence map›Paper›PMID 38631387›Full record

ArticleJournal of the National Comprehensive Cancer Network : JNCCN2024

Racial Differences in Germline Genetic Testing Completion Among Males With Pancreatic, Breast, or Metastatic Prostate Cancers.

Jeffrey W Shevach, Danielle Candelieri-Surette, Julie A Lynch, Rebecca A Hubbard, Patrick R Alba, Karen Glanz, Ravi B Parikh, Kara N Maxwell

Open access · bronzeAbstract read
In one paragraph

Article in Journal of the National Comprehensive Cancer Network : JNCCN, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
6.6field-weighted citation impact, top 3% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

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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

8 authors at 5 institutions in 1 country.

Jeffrey W ShevachDivision of Medical Oncology, Department of Medicine, Duke University, Durham, NC.
Danielle Candelieri-SuretteVA Informatics and Computing Infrastructure, VA Salt Lake City Health Care System, Salt Lake City, UT.
Julie A LynchVA Informatics and Computing Infrastructure, VA Salt Lake City Health Care System, Salt Lake City, UT.
Rebecca A HubbardDepartment of Biostatistics, Epidemiology & Informatics, University of Pennsylvania, Philadelphia, PA.
Patrick R AlbaVA Informatics and Computing Infrastructure, VA Salt Lake City Health Care System, Salt Lake City, UT.
Karen GlanzPerelman School of Medicine and School of Nursing, University of Pennsylvania, Philadelphia, PA.
Ravi B ParikhCorporal Michael J. Crescenz VA Medical Center, Philadelphia, PA.
Kara N MaxwellCorporal Michael J. Crescenz VA Medical Center, Philadelphia, PA.
University of Pennsylvania · USUniversity of Utah · USDuke Medical Center · USPhiladelphia VA Medical Center · USVA Salt Lake City Healthcare System · US

Funding

CANCER CLINICAL EPIDEMIOLOGY TRAINING GRANTT32CA009679 · NCI · UNIVERSITY OF PENNSYLVANIA · PI Richard Aplenc, Karen Glanz · 1992 to 2026
$11.1M
Postdoctoral Training Program in Genomic MedicineT32HG009495 · NHGRI · UNIVERSITY OF PENNSYLVANIA · PI Katherine L. Nathanson, Bogdan Pasaniuc · 2017 to 2026
$4.2M
Human-Machine Collaborations to Improve Prognosis and Clinical Decision-Making in Advanced CancerK08CA263541 · NCI · UNIVERSITY OF PENNSYLVANIA · PI PARIKH, RAVI BHARAT · 2021 to 2025
$1.2M
A genotype-phenotype study of tumors from patients with inherited mutations in DNA repair genesK08CA215312 · NCI · UNIVERSITY OF PENNSYLVANIA · PI MAXWELL, KARA N · 2018 to 2022
$924k
NCI NIH HHS K08 CA215312NCI NIH HHS K08 CA263541NCI NIH HHS T32 CA009679NHGRI NIH HHS T32 HG009495
6 · The paper itself

Abstract

backgroundGermline genetic testing is a vital component of guideline-recommended cancer care for males with pancreatic, breast, or metastatic prostate cancers. We sought to determine whether there were racial disparities in germline genetic testing completion in this population. PATIENTS AND

methodsThis retrospective cohort study included non-Hispanic White and Black males with incident pancreatic, breast, or metastatic prostate cancers between January 1, 2019, and September 30, 2021. Two nationwide cohorts were examined: (1) commercially insured individuals in an administrative claims database, and (2) Veterans receiving care in the Veterans Health Administration. One-year germline genetic testing rates were estimated by using Kaplan-Meier methods. Cox proportional hazards regression was used to test the association between race and genetic testing completion. Causal mediation analyses were performed to investigate whether socioeconomic variables contributed to associations between race and germline testing.

resultsOur cohort consisted of 7,894 males (5,142 commercially insured; 2,752 Veterans). One-year testing rates were 18.0% (95% CI, 16.8%-19.2%) in commercially insured individuals and 14.2% (95% CI, 11.5%-15.0%) in Veterans. Black race was associated with a lower hazard of testing among commercially insured individuals (adjusted hazard ratio [aHR], 0.73; 95% CI, 0.58-0.91; P=.005) but not among Veterans (aHR, 0.99; 95% CI, 0.75-1.32; P=.960). In commercially insured individuals, income (aHR, 0.90; 95% CI, 0.86-0.96) and net worth (aHR, 0.92; 95% CI, 0.86-0.98) mediated racial disparities, whereas education (aHR, 0.98; 95% CI, 0.94-1.01) did not.

conclusionsOverall rates of guideline-recommended genetic testing are low in males with pancreatic, breast, or metastatic prostate cancers. Racial disparities in genetic testing among males exist in a commercially insured population, mediated by net worth and household income; these disparities are not seen in the equal-access Veterans Health Administration. Alleviating financial and access barriers may mitigate racial disparities in genetic testing.

Indexed as

Breast Neoplasms, MaleGenetic TestingPancreatic NeoplasmsProstatic NeoplasmsAdultAgedBlack or African AmericanBreast NeoplasmsGenetic Predisposition to DiseaseGerm-Line MutationHealthcare DisparitiesHumansMaleMiddle AgedRetrospective StudiesUnited States

Identifiers

PMID38631387
PMCPMC11361447
OpenAlexW4394872523

What OpenQuestion holds

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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.