Grant Details
Grant Number: |
5R01CA207365-05 Interpret this number |
Primary Investigator: |
Rebbeck, Timothy |
Organization: |
Dana-Farber Cancer Inst |
Project Title: |
Precision Assessment and Delivery of Cancer Risks in Brca 1/2 Mutation Cancers |
Fiscal Year: |
2021 |
Abstract
Project Summary
In current risk assessment and counseling practices, all women who test positive for a
deleterious BRCA1/2 mutation are quoted the same general range of ovarian cancer risk and
are given the same recommendation regarding utilization of risk reducing salpingo-
oophorectomy (RRSO) and other preventive measures. We have recently published a model
that reports substantial and clinically relevant differences in risk depending on the specific
mutation a woman has inherited. In particular, we have recently shown that specific mutations
confer an increased risk or earlier age of onset for breast or ovarian cancer compared with the
generic risk estimates made for any BRCA1/2 mutation. In addition, risk estimates that consider
previous exposure to important risk factors (e.g., reproductive history, oral contraceptive use, or
preventive surgery use) may have a large impact on cancer risk estimates in this population.
More precise risk information could be critical for optimal decision-making for women who are
considering cancer prevention strategies.
Based on these initial observations, we propose to develop precision absolute risk
models that incorporate information about mutation risk group, to apply in vitro methods to
identify new clinically relevant BRCA1/2 mutations and validate their capacity to cause disease,
and to gain a better understanding of how personal values affect how individual women interpret
and act on risk estimates, for use in a future decision aid intervention. Thus, this proposal will
develop a “precision prevention” approach to BRCA1/2-associated cancer risk to lower the
chances a woman will die from ovarian cancer, and will have immediate translational impact for
women with BRCA1/2 mutations.
Publications
Germline sequence variation in cancer genes in Rwandan breast and prostate cancer cases.
Authors: Manirakiza A.V.
, Baichoo S.
, Uwineza A.
, Dukundane D.
, Uwinkindi F.
, Ngendahayo E.
, Rubagumya F.
, Muhawenimana E.
, Nsabimana N.
, Nzeyimana I.
, et al.
.
Source: Npj Genomic Medicine, 2024-11-24 00:00:00.0; 9(1), p. 61.
EPub date: 2024-11-24 00:00:00.0.
PMID: 39582020
Related Citations
Optimal sampling for positive only electronic health record data.
Authors: Lee S.H.
, Ma Y.
, Wei Y.
, Chen J.
.
Source: Biometrics, 2023-01-11 00:00:00.0; , .
EPub date: 2023-01-11 00:00:00.0.
PMID: 36632649
Related Citations
Reply to V. Fallet et al.
Authors: Li S.
, Silvestri V.
, Rebbeck T.R.
, Neuhausen S.L.
, Hopper J.L.
, Nielsen H.R.
, Ottini L.
, Antoniou A.C.
.
Source: Journal Of Clinical Oncology : Official Journal Of The American Society Of Clinical Oncology, 2022-08-01 00:00:00.0; 40(22), p. 2509-2510.
EPub date: 2022-05-12 00:00:00.0.
PMID: 35549306
Related Citations
The tumor mutational landscape of BRCA2-deficient primary and metastatic prostate cancer.
Authors: Kensler K.H.
, Baichoo S.
, Pathania S.
, Rebbeck T.R.
.
Source: Npj Precision Oncology, 2022-06-17 00:00:00.0; 6(1), p. 39.
EPub date: 2022-06-17 00:00:00.0.
PMID: 35715489
Related Citations
Cancer in sub-Saharan Africa: a Lancet Oncology Commission.
Authors: Ngwa W.
, Addai B.W.
, Adewole I.
, Ainsworth V.
, Alaro J.
, Alatise O.I.
, Ali Z.
, Anderson B.O.
, Anorlu R.
, Avery S.
, et al.
.
Source: The Lancet. Oncology, 2022 06; 23(6), p. e251-e312.
EPub date: 2022-05-09 00:00:00.0.
PMID: 35550267
Related Citations
Cancer Risks Associated With BRCA1 and BRCA2 Pathogenic Variants.
Authors: Li S.
, Silvestri V.
, Leslie G.
, Rebbeck T.R.
, Neuhausen S.L.
, Hopper J.L.
, Nielsen H.R.
, Lee A.
, Yang X.
, McGuffog L.
, et al.
.
Source: Journal Of Clinical Oncology : Official Journal Of The American Society Of Clinical Oncology, 2022-05-10 00:00:00.0; 40(14), p. 1529-1541.
EPub date: 2022-01-25 00:00:00.0.
PMID: 35077220
Related Citations
Therapeutic implications of germline vulnerabilities in DNA repair for precision oncology.
Authors: Shah S.M.
, Demidova E.V.
, Lesh R.W.
, Hall M.J.
, Daly M.B.
, Meyer J.E.
, Edelman M.J.
, Arora S.
.
Source: Cancer Treatment Reviews, 2022 Mar; 104, p. 102337.
EPub date: 2022-01-05 00:00:00.0.
PMID: 35051883
Related Citations
Risk factors for an advanced breast cancer diagnosis within 2 years of a negative mammogram.
Authors: McCarthy A.M.
, Ehsan S.
, Appel S.
, Welch M.
, He W.
, Bahl M.
, Chen J.
, Lehman C.D.
, Armstrong K.
.
Source: Cancer, 2021-09-15 00:00:00.0; 127(18), p. 3334-3342.
EPub date: 2021-06-01 00:00:00.0.
PMID: 34061353
Related Citations
Phenotyping issues for exploring electronic health records to design clinical trials.
Authors: Schnall J.
, Zhang L.
, Chen J.
.
Source: Clinical Trials (london, England), 2020 08; 17(4), p. 402-404.
EPub date: 2020-06-10 00:00:00.0.
PMID: 32522027
Related Citations
A pedigree-based prediction model identifies carriers of deleterious de novo mutations in families with Li-Fraumeni syndrome.
Authors: Gao F.
, Pan X.
, Dodd-Eaton E.B.
, Recio C.V.
, Montierth M.D.
, Bojadzieva J.
, Mai P.L.
, Zelley K.
, Johnson V.E.
, Braun D.
, et al.
.
Source: Genome Research, 2020 Aug; 30(8), p. 1170-1180.
EPub date: 2020-08-18 00:00:00.0.
PMID: 32817165
Related Citations
Legacy Genetic Testing Results for Cancer Susceptibility: How Common are Conflicting Classifications in a Large Variant Dataset from Multiple Practices?
Authors: Yin K.
, Liu Y.
, Lamichhane B.
, Sandbach J.F.
, Patel G.
, Compagnoni G.
, Kanak R.H.
, Rosen B.
, Ondrula D.P.
, Smith L.
, et al.
.
Source: Annals Of Surgical Oncology, 2020-04-27 00:00:00.0; , .
EPub date: 2020-04-27 00:00:00.0.
PMID: 32342295
Related Citations
Precision prophylaxis: Identifying the optimal timing for risk-reducing salpingo-oophorectomy based on type of BRCA1 and BRCA2 cluster region mutations.
Authors: Solsky I.
, Chen J.
, Rebbeck T.R.
.
Source: Gynecologic Oncology, 2020 02; 156(2), p. 363-376.
EPub date: 2020-01-07 00:00:00.0.
PMID: 31918993
Related Citations
Novel Two-Phase Sampling Designs for Studying Binary Outcomes.
Authors: Wang L.
, Williams M.L.
, Chen Y.
, Chen J.
.
Source: Biometrics, 2019-08-26 00:00:00.0; , .
EPub date: 2019-08-26 00:00:00.0.
PMID: 31449330
Related Citations
BRCA1 and BRCA2 Pathogenic Sequence Variants in Women of African Origin or Ancestry.
Authors: Friebel T.M.
, Andrulis I.L.
, Balmaña J.
, Blanco A.M.
, Couch F.J.
, Daly M.B.
, Domchek S.M.
, Easton D.F.
, Foulkes W.D.
, Ganz P.A.
, et al.
.
Source: Human Mutation, 2019-05-21 00:00:00.0; , .
EPub date: 2019-05-21 00:00:00.0.
PMID: 31112363
Related Citations