Grant Number:	1R01CA190871-01 Interpret this number
Primary Investigator:	Bradbury, Angela
Organization:	University Of Pennsylvania
Project Title:	Returning Genetic Research Panel Results for Breast Cancer Susceptibility
Fiscal Year:	2014

DESCRIPTION (provided by applicant): Genetic screening for cancer susceptibility (e.g. BRCA1/2) has become a standard evidence-based practice in cancer prevention and has proven to reduce breast cancer morbidity and mortality. Yet, most individuals and families in whom genetic susceptibility is suspected do not have a BRCA1/2 mutation. Research employing next generation sequencing has revealed that mutations in other genes, such as PALB2, CHEK2 and ATM are associated with elevated risks of breast cancer. Thus, multiplex panels have been developed to efficiently screen a large number of genes simultaneously, including genes of varied penetrance and cancer spectrum and presenting challenges to informed consent and genetic counseling. Despite no clear evidence of clinical utility for many of these genes, these gene panels are now commercially available and increasingly utilized. As large prospective cohort studies with banked DNA have become increasingly utilized to evaluate the effects of genes, the environment and lifestyle, there has been debate over the obligations, if any, to share individual research results (IRR) with research participants. As multiplex panels for breast cancer susceptibility illustrate, some genetic research findings will be associated with health outcomes and/or become available for clinical testing. Yet, there is no consensus on if, how, when and what information should be returned to research participants as these tests become clinically available. Further, the associated costs of returning IRR are unknown, and who should bear the costs of these activities has not been resolved. The overall goal of the proposed longitudinal multi-center study is to evaluate the risks, benefits, utilities and costs of returning multiplex genetic research results for breast cancer susceptibility to geographically and sociodemographically diverse research populations. Our theoretical model grounded in the Self- Regulation Theory of Health Behavior was developed to inform the selection of the short-term and longitudinal outcomes and potential mediators and moderators of these outcomes to inform the debate over risks, benefits and utility of returning IRR. Additionally, we include a broadened conceptualization of the "actual" utility of genomic test results. In Aim 1, we will evaluate uptake of IRR among research participants (Aim 1a), and factors associated with uptake (Aim 1b). In Aim 2, we will evaluate the short-term (Aim 2a) and longitudinal (Aim 2b) risks and benefits (i.e. patients understanding, reactions to, use and perceived utility of genomic information) of returning multiplex genetic research results. We will also evaluate the moderators of these outcomes (e.g. subgroups for whom the return of IRR is more or less beneficial). Equally important we will examine the short-term and longitudinal participant costs, research team costs and medical care utilization and costs with return or IRR (Aim 3a) and moderators of these costs (Aim 3b). We expect this research to inform the ongoing debate and ultimately evidence based guidelines for return of individual genomic research results.




Uptake of Genetic Research Results and Patient-Reported Outcomes With Return of Results Incorporating Web-Based Predisclosure Education.
Authors: Kilbride M. , Egleston B.L. , Chung W.K. , Olopade O. , Maxwell K.N. , Shah P. , Churpek J.E. , Fleisher L. , Terry M.B. , Fetzer D. , et al. .
Source: Journal Of Clinical Oncology : Official Journal Of The American Society Of Clinical Oncology, 2023-11-01 00:00:00.0; 41(31), p. 4905-4915.
EPub date: 2023-08-23 00:00:00.0.
PMID: 37611220
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Development of a tiered and binned genetic counseling model for informed consent in the era of multiplex testing for cancer susceptibility.
Authors: Bradbury A.R. , Patrick-Miller L. , Long J. , Powers J. , Stopfer J. , Forman A. , Rybak C. , Mattie K. , Brandt A. , Chambers R. , et al. .
Source: Genetics In Medicine : Official Journal Of The American College Of Medical Genetics, 2015 Jun; 17(6), p. 485-92.
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Implementation and outcomes of telephone disclosure of clinical BRCA1/2 test results.
Authors: Patrick-Miller L. , Egleston B.L. , Daly M. , Stevens E. , Fetzer D. , Forman A. , Bealin L. , Rybak C. , Peterson C. , Corbman M. , et al. .
Source: Patient Education And Counseling, 2013 Dec; 93(3), p. 413-9.
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Controversies in communication of genetic screening results for cancer: a report from the American Society of Preventive Oncology's Screening Special Interest Group (ASPO's 33rd Annual Meeting, March 8 to 10, 2009, Tampa, Florida).
Authors: Patrick-Miller L. , Bradbury A.R. , Terry M.B. .
Source: Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology, 2010 Feb; 19(2), p. 624-7.
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Uptake and timing of bilateral prophylactic salpingo-oophorectomy among BRCA1 and BRCA2 mutation carriers.
Authors: Bradbury A.R. , Ibe C.N. , Dignam J.J. , Cummings S.A. , Verp M. , White M.A. , Artioli G. , Dudlicek L. , Olopade O.I. .
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