Goyal Ravi K, Chen Hua, Abughosh Susan M, Holmes Holly M, Candrilli Sean D, Johnson Michael L
Department of Pharmaceutical Health Outcomes and Policy, College of Pharmacy, University of Houston, Houston, Texas, USA.
RTI Health Solutions, Research Triangle Park, North Carolina, USA.
Cancer. 2023 Apr 1;129(7):1051-1063. doi: 10.1002/cncr.34675. Epub 2023 Feb 9.
Evidence on overall survival (OS) with cyclin-dependent kinase 4 and 6 (CDK4/6) inhibitors is generally limited to data from clinical trials or a few observational studies with limited generalizability to Medicare population. The aim of this study was to determine OS benefits associated with CDK4/6 inhibitors in older Medicare patients with hormone receptor (HR)-positive and human epidermal growth factor receptor-2 overexpressing (HER2-) metastatic breast cancer (MBC).
In a retrospective cohort design, female patients aged ≥65 years with diagnosis of HR+/HER2- MBC from 2015 to 2017 who initiated first-line systemic therapy within 12 months of MBC diagnosis were selected from the Survey Epidemiology and End Results-Medicare database. The effect of treatment type (endocrine therapy [ET]+CDK4/6 inhibitor vs. ET alone) on OS was analyzed using Kaplan-Meier methods and multivariable Cox regression models. Adjusted hazard ratio (aHR) and 95% CIs were estimated.
A total of 630 eligible patients were identified (169 patients treated with ET+CDK4/6 inhibitor and 461 patients treated with ET alone). In the Kaplan-Meier analysis, OS rate at 3 years after first-line treatment initiation was 73.0% for ET+CDK4/6 inhibitor versus 49.1% for ET alone (log-rank p < .0001). In Cox regression analysis, first-line ET+CDK4/6 inhibitor therapy was associated with 41% lower rate of mortality versus ET alone (aHR, 0.590; 95% CI, 0.423-0.823).
The findings of this real-world study demonstrate significant OS benefit associated with ET+CDK4/6 inhibitor therapy over ET alone in an older Medicare population of patients with HR+/HER2- MBC, largely consistent with the evidence from clinical trials.
细胞周期蛋白依赖性激酶4和6(CDK4/6)抑制剂的总生存期(OS)证据通常仅限于临床试验数据或一些观察性研究,对医疗保险人群的普遍适用性有限。本研究的目的是确定CDK4/6抑制剂在老年医疗保险患者中,对激素受体(HR)阳性且人表皮生长因子受体2过表达(HER2-)的转移性乳腺癌(MBC)患者的OS益处。
采用回顾性队列设计,从监测、流行病学和最终结果-医疗保险数据库中选取2015年至2017年诊断为HR+/HER2-MBC且在MBC诊断后12个月内开始一线全身治疗的65岁及以上女性患者。使用Kaplan-Meier方法和多变量Cox回归模型分析治疗类型(内分泌治疗[ET]+CDK4/6抑制剂与单纯ET)对OS的影响。估计调整后的危险比(aHR)和95%置信区间。
共确定630例符合条件的患者(169例接受ET+CDK4/6抑制剂治疗,461例接受单纯ET治疗)。在Kaplan-Meier分析中,一线治疗开始后3年的OS率,ET+CDK4/6抑制剂组为73.0%,单纯ET组为49.1%(对数秩检验p<0.0001)。在Cox回归分析中,一线ET+CDK4/6抑制剂治疗与单纯ET相比,死亡率降低41%(aHR,0.590;95%置信区间,0.423-0.823)。
这项真实世界研究的结果表明,在老年医疗保险HR+/HER2-MBC患者中,ET+CDK4/6抑制剂治疗与单纯ET相比,具有显著的OS益处,这在很大程度上与临床试验证据一致。