Department of Hospital Pharmaceutics, School of Pharmacy, Showa University, Japan.
Department of Date Science/Pharmacy, National Cancer Center Hospital East, Japan.
Pharmazie. 2021 Sep 1;76(9):450-454. doi: 10.1691/ph.2021.1031.
: The efficacy of docetaxel, cisplatin, and 5-fluorouracil (DCF) therapy in treating esophageal cancer has been reported. However, febrile neutropenia (FN) is a potentially serious adverse event of DCF therapy with an incidence of 10 to 40%. Pegfilgrastim, a granulocyte colony-stimulating factor (G-CSF), has been shown to have a primary prophylactic role in FN. However, it has been suggested that excessive use of expensive G-CSF should be avoided. Therefore, we performed a cost-utility analysis of primary prophylaxis with pegfilgrastim. : Cost-effectiveness analysis using decision tree modelling. : We used a decision tree analysis model based on the report of primary prophylaxis with pegfilgrastim. Based on a previous study, the FN incidence rate was set at 40.0% (95% confidence interval (CI): 11.9-68.1) for the pegfilgrastim group and 43.5% (95%CI: 21.6-65.4) for the no pegfilgrastim group. The FN treatment cost was US$726.63, and the duration of FN was 3.65±1.20 days. The utility value of patients who received DCF therapy was 0.643, and the change in utility value at FN onset was -0.15. Expected cost, quality-adjusted life year (QALY), and incremental cost-effectiveness ratio (ICER) were calculated, and cost-utility analysis was performed. : The ICER of pegfilgrastim was 184,976.75 USD/QALY. As a result of sensitivity analysis, the utility of FN had the greatest impact on the cost-effectiveness analysis, followed by the drug cost of pegfilgrastim. : Primary prophylaxis of FN with pegfilgrastim might not be cost-effectiveness. In determining whether to administer pegfilgrastim it is necessary to consider patient factors, not just the incidence of FN.
多西他赛、顺铂和 5-氟尿嘧啶(DCF)疗法治疗食管癌的疗效已有报道。然而,发热性中性粒细胞减少症(FN)是 DCF 治疗的一种潜在严重不良事件,发生率为 10%至 40%。聚乙二醇化粒细胞集落刺激因子(G-CSF)已被证明在 FN 中有初级预防作用。然而,有人认为应该避免过度使用昂贵的 G-CSF。因此,我们对聚乙二醇化粒细胞集落刺激因子的初级预防进行了成本效用分析。
成本效用分析采用决策树模型。
我们使用了基于聚乙二醇化粒细胞集落刺激因子初级预防报告的决策树分析模型。根据一项先前的研究,FN 发生率在聚乙二醇化粒细胞集落刺激因子组中为 40.0%(95%置信区间(CI):11.9-68.1),在无聚乙二醇化粒细胞集落刺激因子组中为 43.5%(95%CI:21.6-65.4)。FN 治疗费用为 726.63 美元,FN 持续时间为 3.65±1.20 天。接受 DCF 治疗的患者的效用值为 0.643,FN 发病时的效用值变化为-0.15。计算了预期成本、质量调整生命年(QALY)和增量成本效益比(ICER),并进行了成本效用分析。
聚乙二醇化粒细胞集落刺激因子的 ICER 为 184,976.75 美元/QALY。敏感性分析结果表明,FN 的效用对成本效益分析的影响最大,其次是聚乙二醇化粒细胞集落刺激因子的药物成本。
聚乙二醇化粒细胞集落刺激因子预防 FN 的初级预防可能没有成本效益。在决定是否给予聚乙二醇化粒细胞集落刺激因子时,需要考虑患者因素,而不仅仅是 FN 的发生率。