Racial and sociodemographic disparities in the use of targeted therapies in advanced ovarian cancer patients with Medicare

Author:

Knisely AnneORCID,Wu Chi-Fang,Kanbergs Alexa,Agusti NuriaORCID,Jorgensen Kirsten A,Melamed Alexander,Giordano Sharon H,Rauh-Hain Jose Alejandro,Nitecki Wilke RoniORCID

Abstract

ObjectiveTo describe sociodemographic and racial disparities in receipt of poly ADP-ribose polymerase inhibitors (PARPi) and bevacizumab among insured patients with ovarian cancer.MethodsThis retrospective study used the Surveillance, Epidemiology, and End Results (SEER)–Medicare database to identify patients with advanced stage, high grade serous ovarian cancer diagnosed between 2010 and 2019. The primary outcome of interest was receipt of PARPi or bevacizumab at any time after diagnosis. χ2tests were used to compare categorical variables. Factors independently associated with the receipt of PARPi and/or bevacizumab were identified using a multivariable logistic regression.ResultsThe cohort included 6242 patients; 276 (4.4%) received PARPi, 2142 (34.3%) received bevacizumab, and 389 (6.2%) received both. Receipt of either targeted treatment increased over the study period. On univariate analysis, patients who received either targeted therapy were younger (63% vs 48% aged <75 years; p<0.001), had a lower comorbidity index (86% vs 80% Charlson Comorbidity Index 0–1; p<0.001), and higher socioeconomic status (74% vs 71% high socioeconomic status; p=0.047) compared with those who did not receive targeted therapy. In the multivariable model, non-Hispanic black patients were less likely than non-Hispanic white patients to receive either targeted therapy (odds ratio 0.77; 95% confidence interval 0.61 to 0.98; p=0.032). Older patients (aged >74 years) were also less likely to receive PARPi or bevacizumab compared with those aged 65–69 years (all p<0.001).ConclusionSociodemographic and racial disparities exist in receipt of PARPi and bevacizumab among patients with advanced ovarian cancer insured by Medicare. As targeted therapies become more commonly used, a widening disparity gap is likely.

Funder

National Cancer Institute

CDC

Ovarian Cancer Research Program

California Department of Public Health

National Program of Cancer Registries

Department of Public Health

State of California

Centers for Disease Control and Prevention

California Health and Safety Code Section

NIH

Surveillance, Epidemiology and End Results Program

National Institutes of Health

National Institutes of Health/National Cancer Institute

CPRIT

Fundación Alfonso Martin Escudero

Department of Defense

SAC

Publisher

BMJ

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