Evidence map›Paper›PMID 33560870›Full record

ArticleJournal of clinical oncology : official journal of the American Society of Clinical Oncology2021

Time Trends in Receipt of Germline Genetic Testing and Results for Women Diagnosed With Breast Cancer or Ovarian Cancer, 2012-2019.

Allison W Kurian, Kevin C Ward, Paul Abrahamse, Irina Bondarenko, Ann S Hamilton, Dennis Deapen, Monica Morrow, Jonathan S Berek, Timothy P Hofer, Steven J Katz

Registry-linked trialOpen access · greenAbstract readHistorical Article
In one paragraph

Article in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06436157 (Genetic Testing Uptake Through an Enhanced Oncology Nurse-Led Intervention in Patients With Solid Tumors), which is not on this map. Cited by 74 papers.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed
14.7field-weighted citation impact, top 1% 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.

NCT06436157 narecruitingnot on this mapstarted 2024, after this paper: background citation

Genetic Testing Uptake Through an Enhanced Oncology Nurse-Led Intervention in Patients With Solid Tumors (GENESIS): A Pilot Study

TypeinterventionalSponsorUniversity of California, DavisRan2024 to 2025Enrolled60ConditionsSolid Tumor, AdultArmsEnhanced education, Usual care education
3 · Its place in the literature

Who cites it

74 citing papers in PubMed, 109 citations in OpenAlex.

  1. Trial
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  8. Article
  9. Frontiers in oncology · 2026
    Review
  10. International journal of biological sciences · 2026
    Article
  11. Frontiers in oncology · 2026
    Article
  12. Article
  13. Article
  14. Homologous Recombination Deficiency and Survival in Ovarian High-Grade Serous Carcinoma by Self-Reported Race.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2025
    Article
  15. Observational
  16. Observational
  17. Article
  18. Article
  19. Article
  20. Article

14 more citing papers are in PubMed but not listed here.

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

10 authors at 5 institutions in 1 country.

Allison W KurianDepartments of Medicine and of Epidemiology & Population Health, Stanford University, Stanford, CA.ORCID 0000-0002-6175-9470
Kevin C WardDepartment of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, GA.
Paul AbrahamseDepartment of Health Management and Policy, School of Public Health, Department of Biostatistics, University of Michigan, Ann Arbor, MI.ORCID 0000-0001-7433-153X
Irina BondarenkoDepartment of Health Management and Policy, School of Public Health, Department of Biostatistics, University of Michigan, Ann Arbor, MI.
Ann S HamiltonDepartment of Preventive Medicine in the Keck School of Medicine, University of Southern California, Los Angeles, CA.ORCID 0000-0001-5898-2308
Dennis DeapenDepartment of Preventive Medicine in the Keck School of Medicine, University of Southern California, Los Angeles, CA.
Monica MorrowDepartment of Surgery, Memorial Sloan-Kettering Cancer Center, New York, NY.ORCID 0000-0003-4636-8313
Jonathan S BerekDepartment of Obstetrics and Gynecology and Women's Cancer Center, Stanford University, Stanford, CA.
Timothy P HoferDepartment of Internal Medicine, University of Michigan and Center for Clinical Management Research, Veterans Affairs Ann Arbor Healthcare System, Ann Arbor, MI.
Steven J KatzDepartment of Health Management and Policy, School of Public Health, Department of Biostatistics, University of Michigan, Ann Arbor, MI.ORCID 0000-0002-1151-861X
University of Michigan · USStanford University · USUniversity of Southern California · USEmory University · USMemorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
XenograftP30CA046592 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI THEODORE S LAWRENCE · 1988 to 2026
$178.2M
The Challenge of Individualizing Treatments for Patients with Breast CancerP01CA163233 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HOFER, TIMOTHY P. · 2012 to 2016
$13.4M
Genetic testing, treatment use, and mortality after diagnosis of breast and ovarian cancer: The Georgia-California GeneLINK InitiativeR01CA225697 · NCI · STANFORD UNIVERSITY · PI KATZ, STEVEN J., KURIAN, ALLISON W. · 2018 to 2021
$1.6M
NCCDPHP CDC HHS NU58DP006344NCI NIH HHS HHSN261201800003CNCI NIH HHS HHSN261201800009CNCI NIH HHS HHSN261201800009INCI NIH HHS HHSN261201800015CNCI NIH HHS HHSN261201800015INCI NIH HHS HHSN261201800032CNCI NIH HHS HHSN261201800032INCI NIH HHS P01 CA163233NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA046592NCI NIH HHS R01 CA225697
6 · The paper itself

Abstract

purposeGenetic testing is important for breast and ovarian cancer risk reduction and treatment, yet little is known about its evolving use.

methodsSEER records of women of age ≥ 20 years diagnosed with breast or ovarian cancer from 2013 to 2017 in California or Georgia were linked to the results of clinical germline testing through 2019. We measured testing trends, rates of variants of uncertain significance (VUS), and pathogenic variants (PVs).

resultsOne quarter (25.2%) of 187,535 patients with breast cancer and one third (34.3%) of 14,689 patients with ovarian cancer were tested; annually, testing increased by 2%, whereas the number of genes tested increased by 28%. The prevalence of test results by gene category for breast cancer cases in 2017 were

conclusionA testing gap persists for patients with ovarian cancer (34.3% tested

Indexed as

AdultBreast NeoplasmsFemaleGenetic TestingGerm-Line MutationHistory, 21st CenturyHumansOvarian NeoplasmsYoung Adult

Identifiers

PMID33560870
PMCPMC8274804
OpenAlexW3127188239

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.