Literature DB >> 27161971

Health Care Segregation, Physician Recommendation, and Racial Disparities in BRCA1/2 Testing Among Women With Breast Cancer.

Anne Marie McCarthy1, Mirar Bristol2, Susan M Domchek2, Peter W Groeneveld2, Younji Kim2, U Nkiru Motanya2, Judy A Shea2, Katrina Armstrong2.   

Abstract

PURPOSE: Racial disparities in BRCA1/2 testing have been documented, but causes of these disparities are poorly understood. The study objective was to investigate whether the distribution of black and white patients across cancer providers contributes to disparities in BRCA1/2 testing. PATIENTS AND METHODS: We conducted a population-based study of women in Pennsylvania and Florida who were 18 to 64 years old and diagnosed with invasive breast cancer between 2007 and 2009, linking cancer registry data, the American Medical Association Physician Masterfile, and patient and physician surveys. The study included 3,016 women (69% white, 31% black), 808 medical oncologists, and 732 surgeons.
RESULTS: Black women were less likely to undergo BRCA1/2 testing than white women (odds ratio [OR], 0.40; 95% CI, 0.34 to 0.48; P < .001). This difference was attenuated but not eliminated by adjustment for mutation risk, clinical factors, sociodemographic characteristics, and attitudes about testing (OR, 0.66; 95% CI, 0.53 to 0.81; P < .001). The care of black and white women was highly segregated across surgeons and oncologists (index of dissimilarity 64.1 and 61.9, respectively), but adjusting for clustering within physician or physician characteristics did not change the size of the testing disparity. Black women were less likely to report that they had received physician recommendation for BRCA1/2 testing even after adjusting for mutation risk (OR, 0.66; 95% CI, 0.54 to 0.82; P < .001). Adjusting for physician recommendation further attenuated the testing disparity (OR, 0.76; 95% CI, 0.57 to 1.02; P = .06).
CONCLUSION: Although black and white patients with breast cancer tend to see different surgeons and oncologists, this distribution does not contribute to disparities in BRCA1/2 testing. Instead, residual racial differences in testing after accounting for patient and physician characteristics are largely attributable to differences in physician recommendations. Efforts to address these disparities should focus on ensuring equity in testing recommendations.
© 2016 by American Society of Clinical Oncology.

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Year:  2016        PMID: 27161971      PMCID: PMC5012689          DOI: 10.1200/JCO.2015.66.0019

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  58 in total

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4.  Barriers to genetic testing for breast cancer risk among ethnic minority women: an exploratory study.

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7.  Frequency of breast cancer attributable to BRCA1 in a population-based series of American women.

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9.  Early adoption of BRCA1/2 testing: who and why.

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Journal:  J Clin Oncol       Date:  2019-04-09       Impact factor: 44.544

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4.  Promoting guideline-based cancer genetic risk assessment for hereditary breast and ovarian cancer in ethnically and geographically diverse cancer survivors: Rationale and design of a 3-arm randomized controlled trial.

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

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Journal:  Cancer       Date:  2017-02-09       Impact factor: 6.860

Review 6.  Disparities in gynecologic cancer genetics evaluation.

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Journal:  Gynecol Oncol       Date:  2019-01-31       Impact factor: 5.482

7.  The big reveal: Family disclosure patterns of BRCA genetic test results among young Black women with invasive breast cancer.

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8.  Racial and Ethnic Differences in Knowledge About One's Dementia Status.

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9.  Genetic Counseling Referral Rates in Long-Term Survivors of Triple-Negative Breast Cancer.

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