Literature DB >> 32346886

Predictors of genetic testing uptake in newly diagnosed breast cancer patients.

Mary K Ladd1, Beth N Peshkin1, Claudine Isaacs1, Gillian Hooker1, Shawna Willey1, Heiddis Valdimarsdottir2, Tiffani DeMarco1, Suzanne O'Neill1, Savannah Binion1, Marc D Schwartz1.   

Abstract

BACKGROUND AND OBJECTIVES: Many newly diagnosed breast cancer patients do not receive genetic counseling and testing at the time of diagnosis. We examined predictors of genetic testing (GT) in this population.
METHODS: Within a randomized controlled trial of proactive rapid genetic counseling and testing vs usual care, patients completed a baseline survey within 6 weeks of breast cancer diagnosis but before a definitive survey. We conducted a multinomial logistic regression to identify predictors of GT timing/uptake.
RESULTS: Having discussed GT with a surgeon was a dominant predictor (χ2 (2, N = 320) = 70.13; P < .0001). Among those who discussed GT with a surgeon, patients who had made a final surgery decision were less likely to receive GT before surgery compared with postsurgically (OR [odds ratio] = 0.24; 95% confidence interval [CI] = 0.12-0.49) or no testing (OR = 0.28; 95% CI = 0.14-0.56). Older patients (OR = 0.95; 95% CI = 0.91-0.99) and participants enrolled in New York/New Jersey (OR = 0.22; 95% CI = 0.07-0.72) were less likely to be tested compared with receiving results before surgery. Those with higher perceived risk (OR = 1.02; 95% CI = 1.00-1.03) were more likely to receive results before surgery than to not be tested.
CONCLUSIONS: This study highlights the role of patient-physician communication about GT as well as patient-level factors that predict presurgical GT.
© 2020 Wiley Periodicals, Inc.

Entities:  

Keywords:  BRCA1; BRCA2; breast cancer; genetic counseling; genetic testing; patient-physician communication

Mesh:

Year:  2020        PMID: 32346886      PMCID: PMC7397428          DOI: 10.1002/jso.25956

Source DB:  PubMed          Journal:  J Surg Oncol        ISSN: 0022-4790            Impact factor:   3.454


  50 in total

1.  BRCA1 and BRCA2 Mutation Testing in Young Women With Breast Cancer.

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2.  Randomized noninferiority trial of telephone versus in-person genetic counseling for hereditary breast and ovarian cancer.

Authors:  Marc D Schwartz; Heiddis B Valdimarsdottir; Beth N Peshkin; Jeanne Mandelblatt; Rachel Nusbaum; An-Tsun Huang; Yaojen Chang; Kristi Graves; Claudine Isaacs; Marie Wood; Wendy McKinnon; Judy Garber; Shelley McCormick; Anita Y Kinney; George Luta; Sarah Kelleher; Kara-Grace Leventhal; Patti Vegella; Angie Tong; Lesley King
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3.  Validation of a decisional conflict scale.

Authors:  A M O'Connor
Journal:  Med Decis Making       Date:  1995 Jan-Mar       Impact factor: 2.583

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Review 7.  Patient characteristics as predictors of primary health care preferences: a systematic literature analysis.

Authors:  Hans Peter Jung; Cor Baerveldt; Frede Olesen; Richard Grol; Michel Wensing
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8.  Preoperative genetic testing affects surgical decision making in breast cancer patients.

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Journal:  Gynecol Oncol       Date:  2014-06-05       Impact factor: 5.482

9.  Preoperative genetic testing impacts surgical decision making in BRCA mutation carriers with breast cancer: a retrospective cohort analysis.

Authors:  Siddhartha Yadav; Ashley Reeves; Sarah Campian; Amy Sufka; Dana Zakalik
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10.  Contralateral mastectomy and survival after breast cancer in carriers of BRCA1 and BRCA2 mutations: retrospective analysis.

Authors:  Kelly Metcalfe; Shelley Gershman; Parviz Ghadirian; Henry T Lynch; Carrie Snyder; Nadine Tung; Charmaine Kim-Sing; Andrea Eisen; William D Foulkes; Barry Rosen; Ping Sun; Steven A Narod
Journal:  BMJ       Date:  2014-02-11
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