Disparities in cancer genetics care by race/ethnicity among pan-cancer patients with pathogenic germline variants Journal Article
| Authors: | Liu, Y. L.; Maio, A.; Kemel, Y.; Salo-Mullen, E. E.; Sheehan, M.; Tejada, P. R.; Trottier, M.; Arnold, A. G.; Fleischut, M. H.; Latham, A.; Carlo, M. I.; Murciano-Goroff, Y. R.; Walsh, M. F.; Mandelker, D.; Mehta, N.; Bandlamudi, C.; Arora, K.; Zehir, A.; Berger, M. F.; Solit, D. B.; Aghajanian, C.; Diaz, L. A. Jr; Robson, M. E.; Brown, C. L.; Offit, K.; Hamilton, J. G.; Stadler, Z. K. |
| Article Title: | Disparities in cancer genetics care by race/ethnicity among pan-cancer patients with pathogenic germline variants |
| Abstract: | Background: Germline risk assessment is increasing as part of cancer care; however, disparities in subsequent genetic counseling are unknown. Methods: Pan-cancer patients were prospectively consented to tumor-normal sequencing via custom next generation sequencing panel (Memorial Sloan Kettering-Integrated Mutation Profiling of Actionable Cancer Targets) inclusive of germline analysis of ≥76 genes from January 2015 through December 2019 (97.5% research nonbillable) with protocol for genetics referral. Rates of pathogenic/likely pathogenic germline variants (PVs) and downstream counseling were compared across ancestry groups (mutually exclusive groups based on self-reported race/ethnicity and Ashkenazi Jewish [AJ] heritage) using nonparametric tests and multivariable logistic regression models. Results: Among 15,775 patients (59.6%, non-Hispanic [NH]-White; 15.7%, AJ; 20.5%, non-White [6.9%, Asian; 6.8%, Black/African American (AA); 6.7%, Hispanic; 0.1%, Other], and 4.2%, unknown), 2663 (17%) had a PV. Non-White patients had a lower PV rate (n = 433, 13.4%) compared to NH-Whites (n = 1451, 15.4%) and AJ patients (n = 683, 27.6%), p <.01, with differences in mostly moderate and low/recessive/uncertain penetrance variants. Among 2239 patients with new PV, 1652 (73.8%) completed recommended genetic counseling. Non-White patients had lower rates of genetic counseling (67.7%) than NH-White (73.7%) and AJ patients (78.8%), p <.01, with lower rates occurring in Black/AA (63%) compared to NH-White patients, even after adjustment for confounders (odds ratio, 0.60; 95% confidence interval, 0.37–0.97; p =.036). Non-White, particularly Black/AA and Asian, probands had a trend toward lower rates and numbers of at-risk family members being seen for counseling/genetic testing. Conclusions: Despite minimizing barriers to genetic testing, non-White patients were less likely to receive recommended cancer genetics follow-up, with potential implications for oncologic care, cancer risk reduction, and at-risk family members. Lay summary: Genetic testing is becoming an important part of cancer care, and we wanted to see if genetics care was different between individuals of different backgrounds. We studied 15,775 diverse patients with cancer who had genetic testing using a test called MSK-IMPACT that was covered by research funding. Clinically important genetic findings were high in all groups. However, Black patients were less likely to get recommended counseling compared to White patients. Even after removing many roadblocks, non-White and especially Black patients were less likely to get recommended genetics care, which may affect their cancer treatments and families. © 2022 American Cancer Society. |
| Keywords: | adult; controlled study; human cell; major clinical study; genetics; cancer risk; cancer patient; follow up; prospective study; neoplasm; neoplasms; germ cell; cancer therapy; germ cells; cancer genetics; germ line; risk reduction; genetic screening; funding; ethnicity; african american; patient referral; caucasian; genetic counseling; penetrance; hispanic; nonparametric test; confounding variable; inheritance; disparities; ancestry group; blacks; race/ethnicity; high throughput sequencing; cancer; humans; human; male; female; article; black person; ancestry; protein fingerprinting; hispanic or latino; genetic testing and counseling |
| Journal Title: | Cancer |
| Volume: | 128 |
| Issue: | 21 |
| ISSN: | 0008-543X |
| Publisher: | Wiley Blackwell |
| Date Published: | 2022-11-01 |
| Start Page: | 3870 |
| End Page: | 3879 |
| Language: | English |
| DOI: | 10.1002/cncr.34434 |
| PUBMED: | 36041233 |
| PROVIDER: | scopus |
| PMCID: | PMC10335605 |
| DOI/URL: | |
| Notes: | Article -- Export Date: 1 November 2022 -- Source: Scopus |
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