在美国,与转移性去势敏感前列腺癌发展为去势耐药前列腺癌治疗相关的实际经济负担。

IF 2.3 4区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Deborah R Kaye, Ibrahim Khilfeh, Erik Muser, Laura Morrison, Frederic Kinkead, Patrick Lefebvre, Dominic Pilon, Daniel J George
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引用次数: 0

摘要

背景:下一代成像技术的出现可能会降低非转移性前列腺癌(PC)的发病率,增加转移性前列腺癌病例的识别率,从而导致转移性前列腺癌的两个主要晚期阶段。当转移性阉割敏感性前列腺癌(mCSPC)发展为转移性阉割耐药前列腺癌(mCRPC)时,有必要描述医疗资源利用率(HRU)和成本的变化,以确定当前和新疗法的价值驱动因素:描述mCSPC患者在进展为mCRPC前后的治疗模式、HRU和医疗总成本:方法:利用Flatiron转移性PC核心注册中心(2013年1月1日至2021年12月1日)的临床数据和Komodo Health(2014年1月1日至2021年12月1日)的关联理赔数据,确定从mCSPC进展为mCRPC(进展日期为索引日期)并随后于2017年1月1日/之后开始接受一线mCRPC治疗的患者。治疗模式和全因/PC 相关 HRU 和医疗成本按患者每月 (PPPM) 进行描述,分别在指标前(mCSPC 疾病状态)和指标后(mCRPC 疾病状态)不超过 12 个月的时间内进行描述。费用(支付方角度)包括医疗报销中的服务/程序费用和药房报销中的费用。采用 Wilcoxon 符号秩检验对 mCSPC 和 mCRPC 疾病状态下的连续 HRU 和费用进行比较:在 296 名进展为 mCRPC 的 mCSPC 患者(中位年龄 69.0 岁,60.5% 为白人,15.9% 为黑人)中,使用雄激素剥夺疗法的系统疗法从 mCSPC 疾病状态下的 35.1% 大幅增加到 mCRPC 疾病状态下的 92.9%,而使用雄激素剥夺疗法的单一疗法则分别从 25.7% 下降到 2.4%。虽然有39.2%的患者在mCSPC疾病状态下没有接受过上述疗法,但在转为mCRPC后,这一比例降至4.7%。在 mCSPC 和 mCRPC 疾病状态下,PC 相关门诊的平均就诊天数从 1.57 PPPM 增加到 2.16 PPPM(P < 0.001)。从 mCSPC 疾病状态到 mCRPC 疾病状态,平均全因医疗总成本 PPPM 从 4424 美元(医疗成本:2846 美元)增加到 9717 美元(医疗成本:4654 美元),平均 PC 相关医疗总成本 PPPM 从 2859 美元(医疗成本:1626 美元)增加到 8012 美元(医疗成本:3285 美元;所有 P < 0.001):在这项针对美国临床实践中从mCSPC进展为mCRPC患者的真实世界研究中,近2/3的患者在进展为阉割抵抗前没有接受额外的系统疗法治疗。病情恶化后,与 PC 相关的平均总费用增加了近 3 倍,与 PC 相关的医疗费用增加了 2 倍多。使用额外的系统疗法可能会延迟疾病进展到阉割耐药所需的时间和费用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Real-world economic burden associated with disease progression from metastatic castration-sensitive to castration-resistant prostate cancer on treatment in the United States.

Background: The advent of next-generation imaging will likely reduce nonmetastatic prostate cancer (PC) prevalence and increase identification of metastatic prostate cancer cases, resulting in two predominant advanced stages in the metastatic setting. There is a need to characterize changes in health care resource utilization (HRU) and costs when metastatic castration-sensitive PC (mCSPC) progresses to metastatic castration-resistant PC (mCRPC) to identify value drivers from current and new treatments.

Objective: To describe treatment patterns, HRU, and total health care costs among patients with mCSPC, before and after progression to mCRPC.

Methods: Clinical data from the Flatiron Metastatic PC Core Registry (January 1, 2013, to December 1, 2021) and linked claims from Komodo Health (January 1, 2014, to December 1, 2021) were used to identify patients with progression from mCSPC to mCRPC (date of progression was the index date) and subsequently initiated first-line mCRPC therapy on/after January 1, 2017. Treatment patterns and all-cause/PC-related HRU and health care costs were described per-patient-per-month (PPPM), separately for no more than 12 months pre-index (mCSPC disease state) and post-index (mCRPC disease state). Costs (payer's perspective) included those for services/procedures from medical claims and costs from pharmacy claims. Continuous HRU and costs were compared between the mCSPC and mCRPC disease states using Wilcoxon signed rank tests.

Results: Among 296 patients with mCSPC progressing to mCRPC (median age 69.0 years, 60.5% White, 15.9% Black), use of systemic therapies with androgen deprivation therapy increased dramatically from 35.1% in the mCSPC disease state to 92.9% in the mCRPC disease state, and use of androgen deprivation therapy monotherapy decreased from 25.7% to 2.4%, respectively. Although 39.2% received none of these therapies in the mCSPC disease state, this proportion decreased to 4.7% after transition to mCRPC. The mean number of days with PC-related outpatient visits increased from 1.57 to 2.16 PPPM in the mCSPC and mCRPC disease states (P < 0.001). From the mCSPC to mCRPC disease states, mean all-cause total health care costs PPPM increased from $4,424 (medical costs: $2,846) to $9,717 (medical costs: $4,654), and mean PC-related total health care costs PPPM increased from $2,859 (medical costs: $1,626) to $8,012 (medical costs: $3,285; all P < 0.001).

Conclusions: In this real-world study of patients with disease progression from mCSPC to mCRPC in US clinical practice, nearly 2-in-3 patients did not receive treatment with additional systemic therapies before progression to castration resistance. Post-progression, mean PC-related total costs increased nearly 3-fold, with a more than 2-fold increase in PC-related medical costs. Use of additional systemic therapies may delay the time and cost associated with disease progression to castration resistance.

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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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