Literature DB >> 27552275

Effective Referral of Low-Income Women at Risk for Hereditary Breast and Ovarian Cancer to Genetic Counseling: A Randomized Delayed Intervention Control Trial.

Rena J Pasick1, Galen Joseph1, Susan Stewart1, Celia Kaplan1, Robin Lee1, Judith Luce1, Sharon Davis1, Titas Marquez1, Tung Nguyen1, Claudia Guerra1.   

Abstract

OBJECTIVES: To determine the effectiveness of a statewide telephone service in identifying low-income women at risk for hereditary breast and ovarian cancer and referring them to free genetic counseling.
METHODS: From June 2010 through August 2011, eligible callers to California's toll-free breast and cervical cancer telephone service were screened for their family histories of breast and ovarian cancer. High-risk women were identified and called for a baseline survey and randomization to an immediate offer of genetic counseling or a mailed brochure on how to obtain counseling. Clinic records were used to assess receipt of genetic counseling after 2 months.
RESULTS: Among 1212 eligible callers, 709 (58.5%) agreed to answer family history questions; 102 (14%) were at high risk (25% Hispanic, 46% White, 10% Black, 16% Asian, 3% of other racial/ethnic backgrounds). Of the high-risk women offered an immediate appointment, 39% received counseling during the intervention period, as compared with 4.5% of those receiving the brochure.
CONCLUSIONS: A public health approach to the rare but serious risk of hereditary breast and ovarian cancer can be successful when integrated into the efforts of existing safety net organizations.

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Year:  2016        PMID: 27552275      PMCID: PMC5024372          DOI: 10.2105/AJPH.2016.303312

Source DB:  PubMed          Journal:  Am J Public Health        ISSN: 0090-0036            Impact factor:   9.308


  29 in total

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2.  Recruitment, genetic counseling, and BRCA testing for underserved women at a public hospital.

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3.  A multiple testing procedure for clinical trials.

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4.  Efficient identification and referral of low-income women at high risk for hereditary breast cancer: a practice-based approach.

Authors:  G Joseph; C Kaplan; J Luce; R Lee; S Stewart; C Guerra; R Pasick
Journal:  Public Health Genomics       Date:  2012-04-04       Impact factor: 2.000

5.  Meta-analysis of BRCA1 and BRCA2 penetrance.

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6.  Low rates of African American participation in genetic counseling and testing for BRCA1/2 mutations: racial disparities or just a difference?

Authors:  Chanita Hughes Halbert; Lisa Kessler; Aliya Collier; Benita Weathers; Jill Stopfer; Susan Domchek; Jasmine A McDonald
Journal:  J Genet Couns       Date:  2012-07-12       Impact factor: 2.537

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8.  Evaluation of a breast/ovarian cancer genetics referral screening tool in a mammography population.

Authors:  Cecelia A Bellcross; Amy A Lemke; Laura S Pape; Angela L Tess; Lorraine T Meisner
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9.  Pre-counseling education for low literacy women at risk of Hereditary Breast and Ovarian Cancer (HBOC): patient experiences using the Cancer Risk Education Intervention Tool (CREdIT).

Authors:  Galen Joseph; Mary S Beattie; Robin Lee; Dejana Braithwaite; Carolina Wilcox; Maya Metrikin; Kate Lamvik; Judith Luce
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10.  The BOADICEA model of genetic susceptibility to breast and ovarian cancer.

Authors:  A C Antoniou; P P D Pharoah; P Smith; D F Easton
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  15 in total

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3.  Screening for Individuals at Risk for Hereditary Breast and Ovarian Cancer: A Statewide Initiative, Georgia, 2012-2020.

Authors:  Julia K Veitinger; Alice S Kerber; Sheryl G A Gabram-Mendola; Yuan Liu; Lynn M Durham; Diane Durrence; Alissa K Berzen; Janet Y Shin; Cindy Snyder; Cecelia A Bellcross; Yue Guan
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Review 4.  Initiatives to Scale Up and Expand Reach of Cancer Genomic Services Outside of Specialty Clinical Settings: A Systematic Review.

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5.  Genetic counseling and testing for Asian Americans: a systematic review.

Authors:  Jennifer L Young; Julie Mak; Talia Stanley; Michelle Bass; Mildred K Cho; Holly K Tabor
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6.  Genetic Counseling, Screening and Risk-Reducing Surgery in Patients with Primary Breast Cancer and Germline BRCA Mutations: Unmet Needs in Low- and Middle-Income Countries.

Authors:  Hiba A Moukadem; Ahmad Al Masry; Rula W Atwani; Firas Kreidieh; Lana E Khalil; Rita Saroufim; Sarah Daouk; Iman Abou Dalle; Nagi S El Saghir
Journal:  Eur J Breast Health       Date:  2021-12-30

7.  Population screening to identify women at risk for hereditary breast cancer syndromes: The path forward or the road not taken?

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8.  Advancing precision public health using human genomics: examples from the field and future research opportunities.

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9.  Identification of hereditary cancer in the general population: development and validation of a screening questionnaire for obtaining the family history of cancer.

Authors:  Natalia Campacci; Juliana O de Lima; André L Carvalho; Rodrigo D Michelli; Rafael Haikel; Edmundo Mauad; Danilo V Viana; Matias E Melendez; Fabiana de L Vazquez; Cleyton Zanardo; Rui M Reis; Benedito M Rossi; Edenir I Palmero
Journal:  Cancer Med       Date:  2017-10-21       Impact factor: 4.452

10.  Provider's Perceptions of Barriers and Facilitators for Latinas to Participate in Genetic Cancer Risk Assessment for Hereditary Breast and Ovarian Cancer.

Authors:  Alejandra Hurtado-de-Mendoza; Kristi Graves; Sara Gómez-Trillos; Lyndsay Anderson; Claudia Campos; Chalanda Evans; Selma Stearns; Qi Zhu; Nathaly Gonzalez; Vanessa B Sheppard
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