Health care resource utilization and costs of Medicare-enrolled patients with HR+/HER2- metastatic breast cancer treated with a CDK4/6i in the first-line setting.

IF 2.3 4区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Emma Behan, David L Veenstra, Aasthaa Bansal
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引用次数: 0

Abstract

Background: The introduction of cyclin-dependent kinases 4 and 6 inhibitors (CDK4/6is) has transformed the treatment landscape for patients with hormone receptor positive (HR+) and human epidermal growth factor receptor 2 negative (HER2-) metastatic breast cancer (MBC). To our knowledge, no studies have quantified health care resource utilization (HRU) or economic burden following CDK4/6i initiation in the Medicare population.

Objective: To describe HRU and quantify health care costs among Medicare-enrolled patients with HR+ HER2- MBC treated with CDK4/6is in the first-line setting.

Methods: We conducted a retrospective cohort study on Medicare-enrolled patients with HR+ HER2- MBC who initiated a CDK4/6i in the first-line setting between February 2, 2016, and December 31, 2022, using claims from the Merative MarketScan database. We examined all-cause HRU by summarizing the number of inpatient (IP), outpatient (OP), and emergency department (ED) visits as well as the length of stay during the 6 months following CDK4/6i initiation. Additionally, we assessed all-cause health care costs, including IP, OP, ED, and pharmacy, over the 1 year following CDK4/6i initiation using the Kaplan-Meier sample average estimator to account for censoring. We reported total health care costs as the sum of IP, OP, ED, and pharmacy costs.

Results: 901 patients met the inclusion criteria with a mean age of 74 years (SD = 6.84). Nearly 24% (n = 214) had an IP admission in the 6 months following CDK4/6i initiation. Among patients with an IP admission, the mean number of admissions per patient was 1.65 (SD = 0.98) with a mean length of stay per admission of 5.98 (SD = 6.25) days. Roughly 30% (n = 271) of patients had an ED visit, with a mean of 2.1 (SD = 1.54) visits per patient among those who had a visit. Most patients (n = 868, 96.44%) had an OP service, and among those with an OP service, the mean number of days with OP services was 19.96 (SD = 12.29). Mean total health care costs over the 1-year period following CDK4/6is were $62,228 (95% CI = 52,281-73,029) per patient with the main drivers being OP services ($31,686 [95% CI = 27,168-36,925]) and pharmacy costs ($22,727 [95% CI = 19,273-25,931]).

Conclusions: There are numerous sources of HRU and cost in patients following CDK4/6i initiation in the Medicare population. Patients with HR+ HER2- MBC incur high HRU, providing insights for health care decision-makers to optimize treatment strategies and resource allocation for this population.

医疗保险登记的HR+/HER2-转移性乳腺癌患者在一线接受CDK4/6i治疗的医疗资源利用和成本
背景:细胞周期蛋白依赖性激酶 4 和 6 抑制剂(CDK4/6is)的问世改变了激素受体阳性(HR+)和人表皮生长因子受体 2 阴性(HER2-)转移性乳腺癌(MBC)患者的治疗格局。据我们所知,还没有研究对医疗保险人群开始使用 CDK4/6i 后的医疗资源利用率(HRU)或经济负担进行量化:目的:描述一线使用 CDK4/6i 治疗的 HR+ HER2- MBC 医疗保险参保患者的 HRU 和量化医疗费用:我们利用 Merative MarketScan 数据库中的报销单,对 2016 年 2 月 2 日至 2022 年 12 月 31 日期间在一线接受 CDK4/6i 治疗的 HR+ HER2- MBC 医保参保患者进行了一项回顾性队列研究。我们总结了 CDK4/6i 使用后 6 个月内的住院患者 (IP)、门诊患者 (OP) 和急诊科患者 (ED) 的就诊次数以及住院时间,从而检查了全因 HRU。此外,我们还使用卡普兰-梅耶样本平均估算器评估了 CDK4/6i 使用后 1 年内的全因医疗费用,包括 IP、OP、ED 和药房费用,以考虑人口普查因素。我们将总医疗费用报告为IP、OP、ED和药房费用之和:901 名患者符合纳入标准,平均年龄为 74 岁(SD = 6.84)。近 24% 的患者(n = 214)在使用 CDK4/6i 后的 6 个月内曾入院接受 IP 治疗。在入院的 IP 患者中,每位患者的平均入院次数为 1.65 次(SD = 0.98),每次入院的平均住院时间为 5.98 天(SD = 6.25)。约 30% 的患者(n = 271)曾在急诊室就诊,平均每位患者就诊 2.1 次(SD = 1.54)。大多数患者(n = 868,96.44%)接受过 OP 服务,在接受过 OP 服务的患者中,接受 OP 服务的平均天数为 19.96 天(SD = 12.29)。在 CDK4/6is 后的 1 年期间,每位患者的平均医疗总成本为 62,228 美元(95% CI = 52,281-73,029 美元),其中主要是 OP 服务(31,686 美元 [95% CI = 27,168-36,925 美元] )和药房成本(22,727 美元 [95% CI = 19,273-25,931 美元]):结论:在医保人群中,患者使用 CDK4/6i 后产生的 HRU 和费用来源众多。HR+ HER2- MBC 患者的 HRU 很高,这为医疗决策者优化该人群的治疗策略和资源分配提供了启示。
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来源期刊
Journal of managed care & specialty pharmacy
Journal of managed care & specialty pharmacy Health Professions-Pharmacy
CiteScore
3.50
自引率
4.80%
发文量
131
期刊介绍: JMCP welcomes research studies conducted outside of the United States that are relevant to our readership. Our audience is primarily concerned with designing policies of formulary coverage, health benefit design, and pharmaceutical programs that are based on evidence from large populations of people. Studies of pharmacist interventions conducted outside the United States that have already been extensively studied within the United States and studies of small sample sizes in non-managed care environments outside of the United States (e.g., hospitals or community pharmacies) are generally of low interest to our readership. However, studies of health outcomes and costs assessed in large populations that provide evidence for formulary coverage, health benefit design, and pharmaceutical programs are of high interest to JMCP’s readership.
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