Evidence map›Paper›PMID 42339534›Full record

Trial reportCancer prevention research (Philadelphia, Pa.)2026

The Clinical Application of Refined Risk Estimates Study in BRCA1 and BRCA2 Pathogenic Variant Carriers: A Randomized Controlled Trial.

Leigha Senter, Shelly Hovick, Rachel Notestine, Lauren Norden, Nadia Benny, Shannon Phillips, Ava Willoughby, Robert Pyatt, Doreen Agnese, Julie S Mak and 11 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Cancer prevention research (Philadelphia, Pa.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

21 authors.

Leigha SenterDivision of Human Genetics, Department of Internal Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.ORCID 0000-0001-9270-8847
Shelly HovickSchool of Communication, The Ohio State University, Columbus, Ohio.ORCID 0000-0001-7665-8966
Rachel NotestineDivision of Human Genetics, Department of Internal Medicine, The Ohio State University Wexner Medical Center, Columbus, Ohio.ORCID 0009-0001-5785-7983
Lauren NordenDivision of Human Genetics, Department of Internal Medicine, The Ohio State University Wexner Medical Center, Columbus, Ohio.ORCID 0009-0006-8215-3538
Nadia BennyDivision of Human Genetics, Department of Internal Medicine, The Ohio State University Wexner Medical Center, Columbus, Ohio.ORCID 0009-0002-3654-0191
Shannon PhillipsDivision of Human Genetics, Department of Internal Medicine, The Ohio State University Wexner Medical Center, Columbus, Ohio.ORCID 0000-0001-5207-8983
Ava WilloughbyDivision of Human Genetics, Department of Internal Medicine, The Ohio State University Wexner Medical Center, Columbus, Ohio.ORCID 0009-0005-9312-2078
Robert PyattDepartment of Pathology and Laboratory Medicine, Nationwide Children's Hospital, Columbus, Ohio.ORCID 0000-0002-3042-8492
Doreen AgneseDivision of Surgical Oncology, The Ohio State University Wexner Medical Center, Columbus, Ohio.ORCID 0000-0002-9910-9422
Julie S MakUniversity of California San Francisco Helen Diller Family Comprehensive Cancer Center , San Francisco, California.ORCID 0009-0000-6992-3282
Allison DePersiaNeaman Center for Personalized Medicine Endeavor Health, NorthShore University HealthSystem, Evanston, Illinois.ORCID 0000-0001-8338-3112
Sarah V ColonnaDepartment of Internal Medicine, University of Utah, USA, Salt Lake City, Utah.ORCID 0000-0002-9026-6990
Whitney F MaxwellHuntsman Cancer Institute , University of Utah, USA, Salt Lake City, Utah.ORCID 0000-0002-7159-9239
Wendy KohlmannHuntsman Cancer Institute , University of Utah, USA, Salt Lake City, Utah.ORCID 0000-0002-9134-9640
Erika L SpaethGenetic Technologies Ltd, Charlotte, North Carolina.ORCID 0000-0002-5397-3493
Ora GordonProvidence Saint John's Cancer Institute, Santa Monica, California.ORCID 0009-0002-2084-7914
Darcy ThullDepartment of Hematology/Oncology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.ORCID 0000-0001-7999-2804
Guy N BrockCenter for Biostatistics, College of Medicine, The Ohio State University, Columbus, Ohio.ORCID 0000-0001-5317-079X
Amy WebbDepartment of Biomedical Informatics, The Ohio State University, Columbus, Ohio.ORCID 0000-0001-5503-7300
Rachel M SmithCenter for Biostatistics, College of Medicine, The Ohio State University, Columbus, Ohio.ORCID 0000-0002-8256-5456
Amanda Ewart TolandDivision of Human Genetics, Department of Internal Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.ORCID 0000-0002-0271-1792

Funding

The Ohio State University Center for clinical and Translational ScienceUL1TR001070 · NCATS · OHIO STATE UNIVERSITY · PI JACKSON, REBECCA D · 2013 to 2017
$22.6M
The Ohio State University Center for Clinical and Translational Science (UL1)UL1TR000090 · NCATS · OHIO STATE UNIVERSITY · PI JACKSON, REBECCA D · 2012 to 2013
$7.9M
National Institutes of Health (NIH) 8UL1TR000090-05National Institutes of Health (NIH) UL1TR001070NCATS NIH HHS UL1 TR000090NCATS NIH HHS UL1 TR001070
6 · The paper itself

Abstract

Individuals with germline BRCA1 or BRCA2 pathogenic variants (PV) may struggle with risk management decision-making. Advancements in technology could provide more specific risk information to patients, but the impact of this information is unknown. The Clinical Application of Refined Risk Estimates Study is a two-arm randomized controlled trial in women with a BRCA1/BRCA2 PV. The primary objective was to determine whether genotype-informed personalized cancer risk estimates (GRE) compared with standard lifetime cancer risk estimates (SRE) decreased decisional conflict related to cancer risk management decision-making. Women were recruited following the disclosure of their PV results. Participants completed a baseline survey and were randomized 1:1 to receive a GRE or SRE. After receiving their results, participants completed a follow-up survey. Likert and continuous data measures were analyzed using linear regression. There were no differences in decisional conflict between study arms at follow-up. However, individuals in the SRE arm showed an increased need for personal structure compared with those in the GRE arm (P = 0.02). Compared with baseline, individuals within the SRE arm showed decreased decisional conflict (P = 0.003) and increased perceived stress (P = 0.02) at follow-up. A more personalized cancer risk estimate did not decrease decisional conflict in women with BRCA1/BRCA2 PVs. Future studies will determine whether a GRE affects actual decision-making behaviors. PREVENTION RELEVANCE: Women with a germline PV in BRCA1 or BRCA2 have significantly elevated risks of developing breast and ovarian cancers. This randomized controlled trial evaluates the impact of polygenic risk scores on decisional conflict related to breast and ovarian cancer prevention and risk management in those with BRCA1/BRCA2 PVs.

Indexed as

BRCA1 ProteinBRCA2 ProteinBreast NeoplasmsOvarian NeoplasmsAdultDecision MakingFemaleFollow-Up StudiesGenetic Predisposition to DiseaseGenetic TestingGerm-Line MutationHeterozygoteHumansMiddle AgedReturn of Individual Research ResultsRisk AssessmentBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, human

Identifiers

PMID42339534
PMCPMC13389799

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Registered trials

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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.