Racial Differences in Germline Genetic Testing Completion Among Males With Pancreatic, Breast, or Metastatic Prostate Cancers.

IF 14.8 2区 医学 Q1 ONCOLOGY Journal of the National Comprehensive Cancer Network Pub Date : 2024-04-17 DOI:10.6004/jnccn.2023.7105
Jeffrey W Shevach, Danielle Candelieri-Surette, Julie A Lynch, Rebecca A Hubbard, Patrick R Alba, Karen Glanz, Ravi B Parikh, Kara N Maxwell
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Abstract

Background: Germline genetic testing is a vital component of guideline-recommended cancer care for males with pancreatic, breast, or metastatic prostate cancers. We sought to determine whether there were racial disparities in germline genetic testing completion in this population.

Patients and methods: This retrospective cohort study included non-Hispanic White and Black males with incident pancreatic, breast, or metastatic prostate cancers between January 1, 2019, and September 30, 2021. Two nationwide cohorts were examined: (1) commercially insured individuals in an administrative claims database, and (2) Veterans receiving care in the Veterans Health Administration. One-year germline genetic testing rates were estimated by using Kaplan-Meier methods. Cox proportional hazards regression was used to test the association between race and genetic testing completion. Causal mediation analyses were performed to investigate whether socioeconomic variables contributed to associations between race and germline testing.

Results: Our cohort consisted of 7,894 males (5,142 commercially insured; 2,752 Veterans). One-year testing rates were 18.0% (95% CI, 16.8%-19.2%) in commercially insured individuals and 14.2% (95% CI, 11.5%-15.0%) in Veterans. Black race was associated with a lower hazard of testing among commercially insured individuals (adjusted hazard ratio [aHR], 0.73; 95% CI, 0.58-0.91; P=.005) but not among Veterans (aHR, 0.99; 95% CI, 0.75-1.32; P=.960). In commercially insured individuals, income (aHR, 0.90; 95% CI, 0.86-0.96) and net worth (aHR, 0.92; 95% CI, 0.86-0.98) mediated racial disparities, whereas education (aHR, 0.98; 95% CI, 0.94-1.01) did not.

Conclusions: Overall rates of guideline-recommended genetic testing are low in males with pancreatic, breast, or metastatic prostate cancers. Racial disparities in genetic testing among males exist in a commercially insured population, mediated by net worth and household income; these disparities are not seen in the equal-access Veterans Health Administration. Alleviating financial and access barriers may mitigate racial disparities in genetic testing.

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胰腺癌、乳腺癌或转移性前列腺癌男性患者完成基因检测的种族差异。
背景:对于胰腺癌、乳腺癌或转移性前列腺癌男性患者来说,种系基因检测是指南推荐的癌症治疗的重要组成部分。我们试图确定在这一人群中完成种系基因检测是否存在种族差异:这项回顾性队列研究包括 2019 年 1 月 1 日至 2021 年 9 月 30 日期间罹患胰腺癌、乳腺癌或转移性前列腺癌的非西班牙裔白人和黑人男性。研究对象包括两个全国性队列:(1)行政索赔数据库中的商业保险投保人;(2)在退伍军人健康管理局接受治疗的退伍军人。使用 Kaplan-Meier 方法估算了一年的种系基因检测率。采用 Cox 比例危险回归法检验种族与基因检测完成率之间的关系。我们还进行了因果中介分析,以研究社会经济变量是否会导致种族与种系检测之间的关联:我们的队列由 7894 名男性组成(5142 名有商业保险;2752 名退伍军人)。商业保险人员的一年检测率为 18.0%(95% CI,16.8%-19.2%),退伍军人的一年检测率为 14.2%(95% CI,11.5%-15.0%)。黑色人种与商业保险投保人中较低的检测风险有关(调整后风险比 [aHR],0.73;95% CI,0.58-0.91;P=.005),但与退伍军人中较低的检测风险无关(aHR,0.99;95% CI,0.75-1.32;P=.960)。在参加商业保险的个人中,收入(aHR,0.90;95% CI,0.86-0.96)和净资产(aHR,0.92;95% CI,0.86-0.98)可以调节种族差异,而教育程度(aHR,0.98;95% CI,0.94-1.01)则不能:结论:在男性胰腺癌、乳腺癌或转移性前列腺癌患者中,指南推荐的基因检测总体比率较低。在商业保险人群中,男性在基因检测方面存在种族差异,这种差异受净资产和家庭收入的影响;而在平等就医的退伍军人健康管理局中则没有这种差异。消除经济和获取方面的障碍可减轻基因检测中的种族差异。
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来源期刊
CiteScore
20.20
自引率
0.00%
发文量
388
审稿时长
4-8 weeks
期刊介绍: JNCCN—Journal of the National Comprehensive Cancer Network is a peer-reviewed medical journal read by over 25,000 oncologists and cancer care professionals nationwide. This indexed publication delivers the latest insights into best clinical practices, oncology health services research, and translational medicine. Notably, JNCCN provides updates on the NCCN Clinical Practice Guidelines in Oncology® (NCCN Guidelines®), review articles elaborating on guideline recommendations, health services research, and case reports that spotlight molecular insights in patient care. Guided by its vision, JNCCN seeks to advance the mission of NCCN by serving as the primary resource for information on NCCN Guidelines®, innovation in translational medicine, and scientific studies related to oncology health services research. This encompasses quality care and value, bioethics, comparative and cost effectiveness, public policy, and interventional research on supportive care and survivorship. JNCCN boasts indexing by prominent databases such as MEDLINE/PubMed, Chemical Abstracts, Embase, EmCare, and Scopus, reinforcing its standing as a reputable source for comprehensive information in the field of oncology.
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