Predictors of risk-reducing surgery intentions following genetic counseling for hereditary breast and ovarian cancer.


Journal

Translational behavioral medicine
ISSN: 1613-9860
Titre abrégé: Transl Behav Med
Pays: England
ID NLM: 101554668

Informations de publication

Date de publication:
20 05 2020
Historique:
pubmed: 13 11 2018
medline: 21 7 2021
entrez: 13 11 2018
Statut: ppublish

Résumé

Risk-reducing mastectomy (RRM) and salpingo-oophorectomy (RRSO) are increasingly used to reduce breast and ovarian cancer risk following BRCA1/BRCA2 testing. However, little is known about how genetic counseling influences decisions about these surgeries. Although previous studies have examined intentions prior to counseling, few have examined RRM and RRSO intentions in the critical window between genetic counseling and test result disclosure. Previous research has indicated that intentions at this time point predict subsequent uptake of surgery, suggesting that much decision-making has taken place prior to result disclosure. This period may be a critical time to better understand the drivers of prophylactic surgery intentions. The aim of this study was to examine predictors of RRM and RRSO intentions. We hypothesized that variables from the Health Belief Model would predict intentions, and we also examined the role of affective factors. Participants were 187 women, age 21-75, who received genetic counseling for hereditary breast and ovarian cancer. We utilized multiple logistic regression to identify independent predictors of intentions. 49.2% and 61.3% of participants reported intentions for RRM and RRSO, respectively. Variables associated with RRM intentions include: newly diagnosed with breast cancer (OR = 3.63, 95% CI = 1.20-11.04), perceived breast cancer risk (OR = 1.46, 95% CI = 1.17-1.81), perceived pros (OR = 1.79, 95% CI = 1.38-2.32) and cons of RRM (OR = 0.81, 95% CI = 0.65-0.996), and decision conflict (OR = 0.80, 95% CI = 0.66-0.98). Variables associated with RRSO intentions include: proband status (OR = 0.28, 95% CI = 0.09-0.89), perceived pros (OR = 1.35, 95% CI = 1.11-1.63) and cons of RRSO (OR = 0.72, 95% CI = 0.59-0.89), and ambiguity aversion (OR = 0.79, 95% CI = 0.65-0.95). These data provide support for the role of genetic counseling in fostering informed decisions about risk management, and suggest that the role of uncertainty should be explored further.

Identifiants

pubmed: 30418620
pii: 5172999
doi: 10.1093/tbm/iby101
pmc: PMC7394490
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

337-346

Subventions

Organisme : NCI NIH HHS
ID : P30 CA051008
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA135179
Pays : United States
Organisme : NHGRI NIH HHS
ID : R01 HG005055
Pays : United States

Informations de copyright

© Society of Behavioral Medicine 2018. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

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Auteurs

Mary Kathleen Ladd (MK)

Georgetown Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC.
Jess and Mildred Fisher Center for Hereditary Cancer and Clinical Genomics Research, Georgetown University, Washington, DC.

Beth N Peshkin (BN)

Georgetown Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC.
Jess and Mildred Fisher Center for Hereditary Cancer and Clinical Genomics Research, Georgetown University, Washington, DC.

Leigha Senter (L)

Division of Human Genetics, Department of Internal Medicine and Comprehensive Cancer Center, The Ohio State University, Columbus, OH.

Shari Baldinger (S)

Virgina Piper Cancer Institute, Allina Health, Minneapolis, MN.

Claudine Isaacs (C)

Georgetown Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC.
Jess and Mildred Fisher Center for Hereditary Cancer and Clinical Genomics Research, Georgetown University, Washington, DC.

Hannah Segal (H)

Georgetown Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC.
Jess and Mildred Fisher Center for Hereditary Cancer and Clinical Genomics Research, Georgetown University, Washington, DC.

Samantha Philip (S)

Georgetown Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC.
Jess and Mildred Fisher Center for Hereditary Cancer and Clinical Genomics Research, Georgetown University, Washington, DC.

Chloe Phillips (C)

Georgetown Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC.
Jess and Mildred Fisher Center for Hereditary Cancer and Clinical Genomics Research, Georgetown University, Washington, DC.

Kate Shane (K)

Division of Human Genetics, Department of Internal Medicine and Comprehensive Cancer Center, The Ohio State University, Columbus, OH.

Aimee Martin (A)

Georgetown Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC.
Jess and Mildred Fisher Center for Hereditary Cancer and Clinical Genomics Research, Georgetown University, Washington, DC.

Veronique Weinstein (V)

Georgetown Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC.
Jess and Mildred Fisher Center for Hereditary Cancer and Clinical Genomics Research, Georgetown University, Washington, DC.

Robert Pilarski (R)

Division of Human Genetics, Department of Internal Medicine and Comprehensive Cancer Center, The Ohio State University, Columbus, OH.

Joanne Jeter (J)

Division of Human Genetics, Department of Internal Medicine and Comprehensive Cancer Center, The Ohio State University, Columbus, OH.

Kevin Sweet (K)

Division of Human Genetics, Department of Internal Medicine and Comprehensive Cancer Center, The Ohio State University, Columbus, OH.

Bonnie Hatten (B)

Virgina Piper Cancer Institute, Allina Health, Minneapolis, MN.

Elisabeth J Wurtmann (EJ)

Virgina Piper Cancer Institute, Allina Health, Minneapolis, MN.

Shanda Phippen (S)

Virgina Piper Cancer Institute, Allina Health, Minneapolis, MN.

Della Bro (D)

Virgina Piper Cancer Institute, Allina Health, Minneapolis, MN.

Marc D Schwartz (MD)

Georgetown Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC.
Jess and Mildred Fisher Center for Hereditary Cancer and Clinical Genomics Research, Georgetown University, Washington, DC.

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