Department of Gynecologic Oncology and Reproductive Medicine, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Department of Health Services Research, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Int J Gynecol Cancer. 2024 Nov 4;34(11):1661-1670. doi: 10.1136/ijgc-2024-005599.
To describe sociodemographic and racial disparities in receipt of poly ADP-ribose polymerase inhibitors (PARPi) and bevacizumab among insured patients with ovarian cancer.
This 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. χ tests were used to compare categorical variables. Factors independently associated with the receipt of PARPi and/or bevacizumab were identified using a multivariable logistic regression.
The 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).
Sociodemographic 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.
描述医疗保险覆盖的卵巢癌患者接受聚 ADP-核糖聚合酶抑制剂 (PARPi) 和贝伐珠单抗治疗的社会人口学和种族差异。
本回顾性研究使用监测、流行病学和最终结果 (SEER)-医疗保险数据库,确定 2010 年至 2019 年间诊断为晚期、高级别浆液性卵巢癌的患者。主要观察指标为诊断后任何时间接受 PARPi 或贝伐珠单抗治疗的情况。使用 χ 检验比较分类变量。使用多变量逻辑回归确定与接受 PARPi 和/或贝伐珠单抗治疗相关的独立因素。
该队列包括 6242 名患者;276 名(4.4%)接受 PARPi 治疗,2142 名(34.3%)接受贝伐珠单抗治疗,389 名(6.2%)同时接受两种治疗。接受靶向治疗的患者比例呈上升趋势。单因素分析显示,接受靶向治疗的患者年龄更小(63% vs 48%年龄<75 岁;p<0.001),合并症指数更低(86% vs 80%Charlson 合并症指数 0-1;p<0.001),社会经济地位更高(74% vs 71%高社会经济地位;p=0.047),而未接受靶向治疗的患者则较低。多变量模型显示,非西班牙裔黑人患者接受靶向治疗的可能性低于非西班牙裔白人患者(比值比 0.77;95%置信区间 0.61 至 0.98;p=0.032)。与 65-69 岁患者相比,年龄>74 岁的患者接受 PARPi 或贝伐珠单抗治疗的可能性也较低(均 p<0.001)。
医疗保险覆盖的晚期卵巢癌患者接受 PARPi 和贝伐珠单抗治疗存在社会人口学和种族差异。随着靶向治疗的广泛应用,差异可能会进一步扩大。