Literature DB >> 27117712

Use of Cancer Genetics Services in African-American Young Breast Cancer Survivors.

Tarsha Jones1, Joan S Lockhart2, Kari E Mendelsohn-Victor3, Debra Duquette4, Laurel L Northouse3, Sonia A Duffy5, Rosemary Donley2, Sofia D Merajver6, Kara J Milliron7, J Scott Roberts8, Maria C Katapodi9.   

Abstract

INTRODUCTION: African-American women have higher rates of early-onset breast cancer compared with their Caucasian counterparts; yet, when diagnosed with breast cancer at a young age, they underuse genetic counseling and testing to manage their risk of developing future cancers.
METHODS: Self-reported baseline data were collected between September 2012 and January 2013 and analyzed in 2014 from a subpopulation of 340 African-American young breast cancer survivors (YBCSs) enrolled in an RCT. YBCSs were diagnosed with invasive breast cancer or ductal carcinoma in situ between ages 20 and 45 years and were randomly selected from a statewide cancer registry. Logistic regression examined predictors of using cancer genetics services.
RESULTS: Overall, 28% of the sample reported having genetic counseling and 21% reported having genetic testing, which were significantly lower (p≤0.005) compared with white/other YBCSs participating in the parent study. In a multivariate analysis, income was positively associated with counseling (B=0.254, p≤0.01) and testing (B=0.297, p≤0.01), whereas higher education levels (B=-0.328, p≤0.05) and lack of access to healthcare services owing to cost (B=-1.10, p≤0.03) were negatively associated with genetic counseling. Lower income and lack of care because of high out-of-pocket costs were commonly reported barriers.
CONCLUSIONS: Despite national recommendations for genetic evaluation among women with early-onset breast cancer, few African-American YBCSs reported undergoing genetic counseling and testing. Most reported that their healthcare provider did not recommend these services. Interventions addressing patient, provider, and structural healthcare system barriers to using genetic counseling and testing in this population are needed.
Copyright © 2016 American Journal of Preventive Medicine. All rights reserved.

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Year:  2016        PMID: 27117712     DOI: 10.1016/j.amepre.2016.03.016

Source DB:  PubMed          Journal:  Am J Prev Med        ISSN: 0749-3797            Impact factor:   5.043


  21 in total

1.  Racial disparities in BRCA testing and cancer risk management across a population-based sample of young breast cancer survivors.

Authors:  Deborah Cragun; Anne Weidner; Courtney Lewis; Devon Bonner; Jongphil Kim; Susan T Vadaparampil; Tuya Pal
Journal:  Cancer       Date:  2017-02-09       Impact factor: 6.860

2.  Biospecimen donation among black and white breast cancer survivors: opportunities to promote precision medicine.

Authors:  Vanessa B Sheppard; Alejandra Hurtado-de-Mendoza; Yun-Ling Zheng; Ying Wang; Kristi D Graves; Tania Lobo; Hanfei Xu; Yvonne Jennings; Dennis Tolsma; Martha Trout; Brandi E Robinson; Brittany McKinnon; Mahlet Tadesse
Journal:  J Cancer Surviv       Date:  2017-11-16       Impact factor: 4.442

3.  Mental Illness and BRCA1/2 Genetic Testing Intention Among Multiethnic Women Undergoing Screening Mammography.

Authors:  Tarsha Jones; Katherine Freeman; Marra Ackerman; Meghna S Trivedi; Thomas Silverman; Peter Shapiro; Rita Kukafka; Katherine D Crew
Journal:  Oncol Nurs Forum       Date:  2020-01-01       Impact factor: 2.172

4.  Implementing Cancer Genomics in State Health Agencies: Mapping Activities to an Implementation Science Outcome Framework.

Authors:  Ridgely Fisk Green; Marie T Kumerow; Juan L Rodriguez; Siobhan Addie; Sarah H Beachy; Laura Senier
Journal:  Public Health Genomics       Date:  2020-09-17       Impact factor: 2.000

Review 5.  Care delivery considerations for widespread and equitable implementation of inherited cancer predisposition testing.

Authors:  Deborah Cragun; Anita Y Kinney; Tuya Pal
Journal:  Expert Rev Mol Diagn       Date:  2016-12-13       Impact factor: 5.225

6.  Communicating with Daughters About Familial Risk of Breast Cancer: Individual, Family, and Provider Influences on Women's Knowledge of Cancer Risk.

Authors:  Lucy A Peipins; Juan L Rodriguez; Nikki A Hawkins; Ashwini Soman; Mary C White; M Elizabeth Hodgson; Lisa A DeRoo; Dale P Sandler
Journal:  J Womens Health (Larchmt)       Date:  2018-01-29       Impact factor: 2.681

7.  Patterns of cancer family history and genetic counseling eligibility among African Americans with breast, prostate, lung, and colorectal cancers: A Detroit Research on Cancer Survivors cohort study.

Authors:  Kristen S Purrington; Ann G Schwartz; Julie J Ruterbusch; Mark A Manning; Mrudula Nair; Angela S Wenzlaff; Stephanie S Pandolfi; Michael S Simon; Jennifer Beebe-Dimmer
Journal:  Cancer       Date:  2020-08-04       Impact factor: 6.860

8.  Strategies to enhance identification of hereditary breast cancer gene carriers.

Authors:  Sonya Reid; Lucy B Spalluto; Tuya Pal
Journal:  Expert Rev Mol Diagn       Date:  2020-09-11       Impact factor: 5.225

9.  A comparison of cancer risk assessment and testing outcomes in patients from underserved vs. tertiary care settings.

Authors:  Huma Q Rana; Sarah R Cochrane; Elaine Hiller; Ruth N Akindele; Callie M Nibecker; Ludmila A Svoboda; Angel M Cronin; Judy E Garber; Christopher S Lathan
Journal:  J Community Genet       Date:  2017-11-18

10.  Knowledge and perceptions of BRCA1/2 genetic testing and needs of diverse women with a personal or family history of breast cancer in South Florida.

Authors:  Tarsha Jones; Heather Howard; Katherine Freeman-Costin; Ana Creighton; Karen Wisdom-Chambers; Meghan Underhill-Blazey
Journal:  J Community Genet       Date:  2021-02-08
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