a Modeling and Meta-analysis , Pharmerit International , Bethesda , MD , USA.
b HEOR & Value-Based Medicine , Helsinn Therapeutics (US), Inc , Iselin , NJ , USA.
J Med Econ. 2019 Aug;22(8):840-847. doi: 10.1080/13696998.2019.1620244. Epub 2019 Jun 11.
Chemotherapy-induced nausea and vomiting (CINV) are among the most common and debilitating side-effects patients experience during chemotherapy, and are associated with considerable acute care use and healthcare cost. It is estimated that 70-80% of CINV could be prevented through appropriate use of CINV prophylaxis; however, suboptimal CINV compliance and control remains an issue in clinical practice. Netupitant/palonosetron (NEPA) is a fixed combination of serotonin-3 (5-HT) and neurokinin-1 (NK) receptor antagonists (RAs), respectively, indicated for the prevention of acute and delayed nausea and vomiting associated with highly emetogenic chemotherapy (HEC) and moderately emetogenic chemotherapy (MEC). Phase 3 clinical trials showed a significantly higher complete response rate in both acute and delayed CINV in chemotherapy-naïve patients receiving NEPA compared to patients receiving palonosetron. The objective of this study was to estimate the budgetary impact of adding NEPA to a US payer or practice formulary for CINV prophylaxis. A model was developed to estimate the impact of adding NEPA to the formulary of a hypothetical US payer with 1.15 million members, including 150,000 (13%) Medicare beneficiaries. The model compared the annual total costs of CINV-related events and CINV prophylaxis in two scenarios: base year (no NEPA) and comparator year (10% and 5% NEPA usage in HEC and MEC patients, respectively). A univariate sensitivity analysis was conducted to explore the effect of variability in model parameters on the budget impact. A total of 2,021 patients were eligible to receive CINV prophylaxis. With NEPA, CINV prophylaxis costs increased by 0.7% ($3,493,630 vs $3,518,760) while medical costs associated with CINV events decreased by 3.9% ($15,118,639 vs $14,532,442), resulting in a net cost saving of $561,067 (3.0%) for the health plan ($18,612,269 vs $18,051,202), or $0.04 per member per month. This was equivalent to saving $5,011 per patient moved to NEPA. Among all 5-HT RA + NK RA regimens, NEPA was associated with the lowest CINV-related costs, leading to the lowest total cost of care. Adding NEPA to a payer or practice formulary results in a net decrease in the total budget due to a substantial reduction in CINV event-related resource utilization and medical costs, and an increase in pharmacy costs <1%, saving over $5,000 per patient.
化疗引起的恶心和呕吐 (CINV) 是患者在化疗期间最常见和最具衰弱性的副作用之一,与大量急性护理使用和医疗保健费用相关。据估计,通过适当使用 CINV 预防措施,70-80%的 CINV 可以预防;然而,在临床实践中,CINV 的依从性和控制仍然存在问题。奈妥吡坦/帕洛诺司琼 (NEPA) 是 5-羟色胺-3(5-HT)和神经激肽-1(NK)受体拮抗剂(RAs)的固定组合,分别用于预防与高致吐性化疗(HEC)和中度致吐性化疗(MEC)相关的急性和延迟性恶心和呕吐。III 期临床试验显示,与接受帕洛诺司琼的患者相比,在接受 NEPA 的化疗初治患者中,急性和延迟性 CINV 的完全缓解率显著更高。本研究旨在估算在美国支付者或实践处方中添加 NEPA 用于 CINV 预防的预算影响。建立了一个模型,以估算在一个拥有 115 万成员的假设美国支付者的处方中添加 NEPA 的影响,其中包括 150,000 名(13%)医疗保险受益人。该模型比较了两种情况下与 CINV 相关的事件和 CINV 预防的年度总费用:基础年(无 NEPA)和比较年(HEC 和 MEC 患者中分别使用 10%和 5%的 NEPA)。进行了单变量敏感性分析,以探讨模型参数的变异性对预算影响的影响。共有 2,021 名患者有资格接受 CINV 预防。使用 NEPA,CINV 预防成本增加了 0.7%(3,493,630 美元对 3,518,760 美元),而与 CINV 事件相关的医疗成本下降了 3.9%(15,118,639 美元对 14,532,442 美元),导致健康计划的净节省 561,067 美元(3.0%)(18,612,269 美元对 18,051,202 美元),或每个成员每月 0.04 美元。这相当于将每位患者转移到 NEPA 的费用节省了 5,011 美元。在所有 5-HT RA + NK RA 方案中,NEPA 与最低的 CINV 相关成本相关,导致最低的总护理成本。由于 CINV 事件相关资源利用和医疗成本的大幅减少,以及药房成本增加<1%,在美国支付者或实践处方中添加 NEPA 会导致总预算净减少,每个患者的节省超过 5,000 美元。