Evidence map›Paper›PMID 33277227›Full record

ArticleJournal of geriatric oncology2021

Breast cancer associated pathogenic variants among women 61 years and older with triple negative breast cancer.

Yanin Chávarri-Guerra, Catherine A Marcum, Carolyn B Hendricks, Deborah Wilbur, Terrence Cescon, Christopher Hake, Julio Abugattas, Yenni Rodriguez, Cynthia Villarreal-Garza, Kai Yang and 8 more

Open access · greenAbstract read
In one paragraph

Article in Journal of geriatric oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed, 10 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

18 authors at 10 institutions in 4 countries.

Yanin Chávarri-GuerraDepartment of Hemato-Oncology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico.
Catherine A MarcumCHI Memorial Rees Skillern Cancer Risk and Survivorship Center, Chattanooga, United States.
Carolyn B HendricksMaryland Oncology Hematology, Bethesda, United States.
Deborah WilburOncology Associates at Hall Perrine Cancer Center, Cedar Rapids, United States.
Terrence CesconReading Hospital, West Reading, United States.
Christopher HakeWaukesha Memorial Hospital-Pro Health Care Research Institute, Waukesha, WI, United States.
Julio AbugattasInstituto Nacional de Enfermedades Neoplásicas, Lima, Peru.
Yenni RodriguezInstituo de Cancerología, Medellín, Colombia.
Cynthia Villarreal-GarzaHospital Hellion Zambrano- TecSalud, Monterrey, Mexico.
Kai YangDepartment of Medical Oncology, Division of Clinical Cancer Genomics, City of Hope Comprehensive Cancer Center, Duarte, CA, United States.
Aleck CervantesDepartment of Medical Oncology, Division of Clinical Cancer Genomics, City of Hope Comprehensive Cancer Center, Duarte, CA, United States.
Sharon SandDepartment of Medical Oncology, Division of Clinical Cancer Genomics, City of Hope Comprehensive Cancer Center, Duarte, CA, United States.
Danielle CastilloDepartment of Medical Oncology, Division of Clinical Cancer Genomics, City of Hope Comprehensive Cancer Center, Duarte, CA, United States.
Joseph HerzogDepartment of Medical Oncology, Division of Clinical Cancer Genomics, City of Hope Comprehensive Cancer Center, Duarte, CA, United States.
Janet MokhnatkinDepartment of Medical Oncology, Division of Clinical Cancer Genomics, City of Hope Comprehensive Cancer Center, Duarte, CA, United States.
Mina S SedrakDepartment of Medical Oncology and Therapeutics Research, City of Hope Comprehensive Cancer Center, Duarte, CA, United States.
Enrique Soto-Perez-de-CelisCancer Care in the Elderly Clinic, Department of Geriatrics, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico.
Jeffrey N WeitzelDepartment of Medical Oncology and Therapeutics Research, City of Hope Comprehensive Cancer Center, Duarte, CA, United States. Electronic address: jnweitzel57@gmai.com.
City of Hope · USInstituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán · MXCHI Memorial Medical Group · USHematology Oncology Associates · USHospital Zambrano Hellion · MXInstituto de Cancerología Las Américas · COInstituto Nacional de Enfermedades Neoplásicas · PEMaryland Oncology Hematology · USProHealth Care · USReading Hospital · US

Funding

Transgenic Mouse FacilityP30CA033572 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI STANLEY R. HAMILTON · 1985 to 2026
$86.3M
Oncology Research Career Development ProgramK12CA001727 · NCI · CITY OF HOPE NATIONAL MEDICAL CENTER · PI MORTIMER, JOANNE E. · 1992 to 2024
$14.6M
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
NCI NIH HHS K12 CA001727NCI NIH HHS P30 CA033572NCI NIH HHS RC4 CA153828
6 · The paper itself

Abstract

Women with triple negative breast cancer (TNBC) have a high prevalence of BRCA1 mutations, and current clinical guidelines recommend genetic testing for patients with TNBC aged ≤60 years. However, studies supporting this recommendation have included few older women with TNBC.

methodsGenetic testing results from women aged >60 years with TNBC enrolled in the Clinical Cancer Genomics Community Research Network (CCGCRN) registry were included in this analysis. Prevalence of breast cancer-associated pathogenic variants (PVs) was compared across age groups.

resultsWe identified 151 women with TNBC aged >60 years (median 65 years; SD 5.3). Of these, 130 (86%) underwent genetic testing, and a breast cancer-associated PV was identified in 16 (12.3%; 95% CI 7-19): BRCA1 (n = 6), BRCA2 (n = 5), PALB2 (n = 2), ATM (n = 1) and RAD51C (n = 2). We found no differences in the proportion of patients with close blood relatives with breast (≤50 years) or ovarian cancer (any age) between PV carriers (37.5%) and non-carriers (34.2%) (p = 0.79). Among PV's carriers, the proportion of older women with a BRCA1 PV was lower when compared to younger women (37.5% vs 77.2%; p < 0.01).

conclusionBreast cancer-associated PVs were found in an important proportion of women aged >60 years with TNBC undergoing genetic testing, including greater representation of BRCA2. These results suggest that older women with TNBC should be offered genetic testing, and that their exclusion based on chronologic age alone may not be appropriate.

Indexed as

Breast NeoplasmsOvarian NeoplasmsTriple Negative Breast NeoplasmsAgedFemaleGenetic TestingHumansGermline variantsOlder womenTriple negative breast cancer

Identifiers

PMID33277227
PMCPMC8868493
OpenAlexW3109718887

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.