Evidence map›Paper›PMID 31012959›Full record

ArticleJournal of the American Geriatrics Society2019

The Burden of Breast Cancer Predisposition Variants Across The Age Spectrum Among 10 000 Patients.

Yanin Chavarri-Guerra, Carolyn B Hendricks, Sandra Brown, Catherine Marcum, Mary Hander, Zdenka E Segota, Chris Hake, Sharon Sand, Thomas P Slavin, Arti Hurria and 6 more

Open access · greenAbstract readMulticenter Study
In one paragraph

Article in Journal of the American Geriatrics Society, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Clonal Hematopoiesis and Mosaicism Revealed by a Multi-Tissue Analysis of Constitutional TP53 Status.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2022
    Article
  6. Review
  7. Article
  8. Review
  9. Evaluation of Germline Genetic Testing Criteria in a Hospital-Based Series of Women With Breast Cancer.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2020
    Article
  10. Article
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 at 9 institutions in 2 countries.

Yanin Chavarri-GuerraInstituto Nacional de Ciencias Médicas y Nutrición, Salvador Zubirán, Mexico City, Mexico.
Carolyn B HendricksMaryland Oncology Hematology, Bethesda, Maryland.
Sandra BrownSt. Joseph Hospital and Mission Hospital, Orange, California.
Catherine MarcumHigh Risk Genetics, Survivorship APN, Chattanooga, Tennessee.
Mary HanderKootenai Clinic Cancer Services, Coeur d'Alene, Idaho.
Zdenka E SegotaHoly Cross Medical Group, Fort Lauderdale, Florida.
Chris HakeWaukesha Memorial Hospital-ProHealth Care Research Institute, Waukesha, Wisconsin.
Sharon SandClinical Cancer Genomics, City of Hope Comprehensive Cancer Center, Duarte, California.
Thomas P SlavinClinical Cancer Genomics, City of Hope Comprehensive Cancer Center, Duarte, California.
Arti HurriaClinical Cancer Genomics, City of Hope Comprehensive Cancer Center, Duarte, California.
Enrique Soto-Perez-de-CelisInstituto Nacional de Ciencias Médicas y Nutrición, Salvador Zubirán, Mexico City, Mexico.ORCID 0000-0002-7301-2163
Bita NehorayClinical Cancer Genomics, City of Hope Comprehensive Cancer Center, Duarte, California.
Kenneth B BlanksteinHunterdon Hematology Oncology, Flemington, New Jersey.
Kathleen R BlazerClinical Cancer Genomics, City of Hope Comprehensive Cancer Center, Duarte, California.
Jeffrey N WeitzelClinical Cancer Genomics, City of Hope Comprehensive Cancer Center, Duarte, California.ORCID 0000-0001-6714-092X
Clinical Cancer Genomics Community Research Network
City of Hope · USInstituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán · MXCancer Services · USHoly Cross Hospital · USHunterdon Medical Center · USMaryland Oncology Hematology · USSt. Joseph Hospital · USUniversity of Tennessee at Chattanooga · USWaukesha Memorial Hospital · US

Funding

Cancer Genetics Professional Education in a Global Community of PracticeR25CA171998 · NCI · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI KATHLEEN R. BLAZER · 2013 to 2026
$4.3M
Clinical Cancer Genetics Community Network: A Sustainable Research PartnershipRC4CA153828 · NCI · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI WEITZEL, JEFFREY N · 2010 to 2010
$1.0M
Mentored Clinical Scientist Research Career Development Award (Parent K08)K08CA234394 · NCI · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI SLAVIN, THOMAS PAUL · 2018 to 2019
$498k
NCI NIH HHS K08 CA234394NCI NIH HHS R25 CA171998NCI NIH HHS RC4 CA153828NIH HHS RC4 CA153828
6 · The paper itself

Abstract

BACKGROUND/

objectivesWomen diagnosed with breast cancer (BC) at an older age are less likely to undergo genetic cancer risk assessment and genetic testing since the guidelines and referrals are biased toward earlier age at diagnosis. Thus, we determined the prevalence and type of pathogenic cancer predisposition variants among women with a history of BC diagnosed at the age of 65 years or older vs younger than 65 years.

designProspective registration cohort.

settingThe Clinical Cancer Genomics Community Research Network, including 40 community-based clinics in the United States and 5 in Latin America.

participantsWomen with BC and genetic testing results. MEASUREMENTS: Sociodemographic characteristics, clinical variables, and genetic profiles were compared between women aged 65 years and older and those younger than 65 years at BC diagnosis.

resultsAmong 588 women diagnosed with BC and aged 65 years and older and 9412 diagnosed at younger than 65 years, BC-associated pathogenic variants (PVs) were detected in 5.6% of those aged 65 years and older (n = 33) and 14.2% of those younger than 65 years (n = 1340) (P < .01). PVs in high-risk genes (eg, BRCA1 and BRCA2) represented 81.1% of carriers among women aged 65 years and older (n = 27) and 93.1% of those younger than 65 years (n = 1248) (P = .01). BRCA2 PVs represented 42.4% of high-risk gene findings for those aged 65 years and older, whereas BRCA1 PVs were most common among carriers younger than 65 years (49.7%). PVs (n = 7) in moderate-risk genes represented 21.2% for carriers aged 65 years and older and 7.3% of those younger than 65 years (n = 98; P < .01). CHEK2 PVs were the most common moderate-risk gene finding in both groups.

conclusionClinically actionable BC susceptibility PVs, particularly in BRCA2 and CHEK2, were relatively prevalent among older women undergoing genetic testing. The significant burden of PVs for older women with BC provides a critical reminder to recognize the full spectrum of eligibility and provide genetic testing for older women, rather than exclusion based on chronological age alone. J Am Geriatr Soc 67:884-888, 2019.

Indexed as

Genetic Predisposition to DiseaseRegistriesAgedAge DistributionAge FactorsBiomarkers, TumorBreast NeoplasmsFemaleFollow-Up StudiesGenetic MarkersGenetic TestingGeriatric AssessmentHumansLatin AmericaMorbidityProspective StudiesBiomarkers, TumorGenetic Markersbreast cancergeneticsolder women

Identifiers

PMID31012959
PMCPMC6524775
OpenAlexW2941163483

What OpenQuestion holds

Textmetadata
LicenceTDM
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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.