Disparities in immune and targeted therapy utilization for older US patients with metastatic renal cell carcinoma

Author:

Chow Ryan D1ORCID,Long Jessica B2,Hassan Sirad2,Wheeler Stephanie B34,Spees Lisa P34,Leapman Michael S25,Hurwitz Michael E6,McManus Hannah D7,Gross Cary P26ORCID,Dinan Michaela A28ORCID

Affiliation:

1. Yale School of Medicine , New Haven, CT, USA

2. Yale Cancer Outcomes, Public Policy, and Effectiveness Research Center , New Haven, CT, USA

3. Department of Health Policy and Management, Gillings School of Global Public Health, University of North Carolina at Chapel Hill (UNC-CH) , Chapel Hill, NC, USA

4. Lineberger Comprehensive Cancer Center, UNC-CH , Chapel Hill, NC, USA

5. Department of Urology, Yale School of Medicine , New Haven, CT, USA

6. Department of Internal Medicine, Yale School of Medicine , New Haven, CT, USA

7. Department of Medicine, Duke University School of Medicine , Durham, NC, USA

8. Department of Chronic Disease Epidemiology, Yale School of Public Health , New Haven, CT, USA

Abstract

Abstract Disparities in metastatic renal cell carcinoma (mRCC) outcomes persist in the era of oral anticancer agents (OAAs) and immunotherapies (IOs). We examined variation in the utilization of mRCC systemic therapies among US Medicare beneficiaries from 2015 to 2019. Logistic regression models evaluated the association between therapy receipt and demographic covariates including patient race, ethnicity, and sex. In total, 15 407 patients met study criteria. After multivariable adjustment, non-Hispanic Black race and ethnicity was associated with reduced IO (adjusted relative risk ratio [aRRR] = 0.76, 95% confidence interval [CI] = 0.61 to 0.95; P = .015) and OAA receipt (aRRR = 0.76, 95% CI = 0.64 to 0.90; P = .002) compared with non-Hispanic White race and ethnicity. Female sex was associated with reduced IO (aRRR = 0.73, 95% CI = 0.66 to 0.81; P < .001) and OAA receipt (aRRR = 0.74, 95% CI = 0.68 to 0.81; P < .001) compared with male sex. Thus, disparities by race, ethnicity, and sex were observed in mRCC systemic therapy utilization for Medicare beneficiaries from 2015 to 2019.

Funder

NIH/NCI

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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