Literature DB >> 28669566

Recent Patterns in Genetic Testing for Breast and Ovarian Cancer Risk in the U.S.

Xuesong Han1, Ahmedin Jemal2.   

Abstract

INTRODUCTION: Mutations in BRCA genes are strongly associated with increased risk of breast and ovarian cancer, and it is recommended that women at high risk for these mutations be referred for genetic counseling and testing. The Affordable Care Act (ACA) provision implemented in 2010 eliminated cost sharing for BRCA genetic testing for privately insured women with family history of BRCA-related cancers.
METHODS: Using a nationally representative sample from the National Health Interview Survey, this study examined trends in genetic testing for breast and ovarian cancer risk from 2005 to 2015 among women by family history and insurance status. To assess the impact of the ACA provision, a difference-in-differences strategy was used to compare changes in genetic testing after ACA implementation between women with a family history of breast or ovarian cancer and those with a family history of other cancers, stratified by insurance type. Analyses were conducted in 2016.
RESULTS: Genetic testing for breast and ovarian cancer risk increased among women with private or public insurance, but not among uninsured women. Among privately insured women, those with family history of breast or ovarian cancer experienced a net increase of 2.9 percentage points (p=0.001) over those with a family history of other cancers, but no significant difference was observed among women with public insurance, suggesting a positive effect of the ACA provision.
CONCLUSIONS: This study underscores the continued need to improve access to care for all populations. Future work should monitor the impact of policy on genetic testing among the high-risk population.
Copyright © 2017 American Journal of Preventive Medicine. Published by Elsevier Inc. All rights reserved.

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Mesh:

Year:  2017        PMID: 28669566     DOI: 10.1016/j.amepre.2017.04.014

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


  6 in total

1.  Utilization of genetic testing in breast cancer treatment after implementation of comprehensive multi-disciplinary care.

Authors:  Samfee Doe; Shariska Petersen; Monique Swain
Journal:  Breast J       Date:  2020-01-09       Impact factor: 2.431

2.  Leveraging an Informatics Approach to Identify an Unmet Clinical Need for BRCA1/2 Testing Among Patients With Ovarian Cancer.

Authors:  Stacy W Gray; Rebecca A Ottesen; Madeline Currey; Mihaela Cristea; Janet Nikowitz; Susan Shehayeb; Vanessa Lozano; Julie Hom; Julie Kilburn; Lisa N Lopez; Sam Wing; Ernesto Sosa; Jenny Shen; Michael Morris; Bedros Dilsizian; Thomas Joseph; James Shen; Camille Adeimy; Tanyanika Phillips; Bahareh Bahadini; Joyce C Niland
Journal:  JCO Clin Cancer Inform       Date:  2022-09

3.  Statewide trends and factors associated with genetic testing for hereditary cancer risk in Arkansas 2013-2018.

Authors:  Mahip Acharya; Kristin K Zorn; Melinda E Simonson; Milan Bimali; Gary W Moore; Cheng Peng; Bradley C Martin
Journal:  Hered Cancer Clin Pract       Date:  2022-05-23       Impact factor: 2.164

Review 4.  [Genital metastases from breast cancer: study of 3 cases and literature review].

Authors:  Olfa Zoukar; Anis Haddad; Amira Daldoul; Sonia Zaied; Amina Ben Salem; Ines Zouari; Raja Faleh
Journal:  Pan Afr Med J       Date:  2018-05-04

5.  Challenges and Opportunities in Engaging Primary Care Providers in BRCA Testing: Results from the BFOR Study.

Authors:  Lydia E Pace; Nadine Tung; Yeonsoo S Lee; Jada G Hamilton; Camila Gabriel; Anna Revette; Sahitya Raja; Colby Jenkins; Anthony Braswell; Kelly Morgan; Jeffrey Levin; Jeremy Block; Susan M Domchek; Katherine Nathanson; Heather Symecko; Kelsey Spielman; Beth Karlan; Daniella Kamara; Jenny Lester; Kenneth Offit; Judy E Garber; Nancy L Keating
Journal:  J Gen Intern Med       Date:  2021-06-25       Impact factor: 6.473

Review 6.  Evaluating the role of public health in implementation of genomics-related recommendations: a case study of hereditary cancers using the CDC Science Impact Framework.

Authors:  Ridgely Fisk Green; Mary Ari; Katherine Kolor; W David Dotson; Scott Bowen; Nancy Habarta; Juan L Rodriguez; Lisa C Richardson; Muin J Khoury
Journal:  Genet Med       Date:  2018-06-15       Impact factor: 8.822

  6 in total

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