Evidence map›Paper›PMID 33010199›Full record

ArticleJournal of genetic counseling2021

BRCA1/2 mutations and risk-reducing bilateral salpingo-oophorectomy among Latinas: The UPTAKE study.

Filipa Lynce, Ilana Schlam, Xue Geng, Beth N Peshkin, Sue Friedman, Julie Dutil, Zeina Nahleh, Claudia Campos, Charité Ricker, Patricia Rodriguez and 4 more

Open access · greenAbstract read
In one paragraph

Article in Journal of genetic counseling, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact, top 88% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. 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

14 authors at 8 institutions in 2 countries.

Filipa LynceLombardi Comprehensive Cancer Center and Fisher Center for Hereditary Cancer and Clinical Genomics Research, Georgetown University, Washington, DC, USA.ORCID 0000-0001-6615-7076
Ilana SchlamWashington Cancer Institute, MedStar Washington Hospital Center, Washington, DC, USA.ORCID 0000-0003-4996-0400
Xue GengDepartment of Biostatistics, Bioinformatics and Biomathematics, Georgetown University, Washington, DC, USA.ORCID 0000-0003-4100-9899
Beth N PeshkinLombardi Comprehensive Cancer Center and Fisher Center for Hereditary Cancer and Clinical Genomics Research, Georgetown University, Washington, DC, USA.ORCID 0000-0002-2997-4701
Sue FriedmanForce - Facing Our Risk of Cancer Empowered, Tampa, FL, USA.
Julie DutilCancer Biology Division, Ponce Research Institute, Ponce Health Sciences University, Ponce, PR, USA.
Zeina NahlehCleveland Clinic Florida, Weston, FL, USA.
Claudia CamposNueva Vida, Alexandria, VA, USA.
Charité RickerUniversity of Southern California Keck School of Medicine, Los Angeles, CA, USA.
Patricia RodriguezVirginia Cancer Specialists, Arlington, VA, USA.
Neelima DenduluriVirginia Cancer Specialists, Arlington, VA, USA.
Jaeil AhnDepartment of Biostatistics, Bioinformatics and Biomathematics, Georgetown University, Washington, DC, USA.ORCID 0000-0001-7998-4759
Claudine IsaacsLombardi Comprehensive Cancer Center and Fisher Center for Hereditary Cancer and Clinical Genomics Research, Georgetown University, Washington, DC, USA.ORCID 0000-0002-9646-1260
Kristi D GravesLombardi Comprehensive Cancer Center and Fisher Center for Hereditary Cancer and Clinical Genomics Research, Georgetown University, Washington, DC, USA.ORCID 0000-0001-8808-1631
Georgetown University · USVirginia Cancer Specialists · USCleveland Clinic Florida · USFacing Our Risk of Cancer Empowered · USMedStar Washington Hospital Center · USNueva Vida · USPonce Health Sciences University · PRUniversity of Southern California · US

Funding

Tissue Culture Shared ResourceP30CA051008 · NCI · GEORGETOWN UNIVERSITY · PI STEPHEN W BYERS · 1990 to 2026
$71.5M
NCI NIH HHS GR 411788NCI NIH HHS P30 CA051008NCI NIH HHS P30CA051008
6 · The paper itself

Abstract

Bilateral salpingo-oophorectomy (BSO) is a risk management approach with strong evidence of mortality reduction for women with germline mutations in the tumor suppressor genes BRCA1 and BRCA2 (BRCA1/2). Few studies to date have evaluated uptake of BSO in women from diverse racial and ethnic backgrounds who carry BRCA1/2 mutations. The objective of the UPTAKE study was to explore rates and predictors of risk-reducing BSO among Latinas affected and unaffected with breast cancer who had a deleterious BRCA1/2 mutation. We recruited 100 Latina women with deleterious BRCA1/2 mutations from community hospitals, academic health systems, community, and advocacy organizations. Women completed interviews in Spanish or English. We obtained copies of genetic test reports for participants who provided signed medical release. After performing threefold cross-validation LASSO for variable selection, we used multiple logistic regression to identify demographic and clinical predictors of BSO. Among 100 participants, 68 had undergone BSO at the time of interview. Of these 68, 35 were US-born (61% of all US-born participants) and 33 were not (77% of the non-US-born participants). Among Latinas with BRCA1/2 mutations, older age (p = 0.004), personal history of breast cancer (p = 0.003), higher income (p = 0.002), and not having a full-time job (p = 0.027) were identified as variables significantly associated with uptake of BSO. Results suggest a high rate of uptake of risk-reducing BSO among a sample of Latinas with BRCA1/2 mutations living in the US. We document factors associated with BSO uptake in a diverse sample of women. Relevant to genetic counseling, our findings identify possible targets for supporting Latinas' decision-making about BSO following receipt of a positive BRCA1/2 test.

Indexed as

Breast NeoplasmsHispanic or LatinoOvarian NeoplasmsBRCA1 ProteinBRCA2 ProteinFemaleGenetic Predisposition to DiseaseHumansMutationOvariectomySalpingo-oophorectomyBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, humanattitudesbilateral salpingo-oophorectomyBRCA1BRCA2disparitiesgenetic counselinggenetic testinghereditary breast and ovarian cancerrisk managementunderrepresented populations

Identifiers

PMID33010199
PMCPMC10064975
OpenAlexW3089493989

What OpenQuestion holds

Textmetadata
LicenceTDM
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.