Lyman G H, Lyman C G, Sanderson R A, Balducci L
Department of Internal Medicine, University of South Florida College of Medicine, Tampa 33612.
J Natl Cancer Inst. 1993 Mar 17;85(6):488-93. doi: 10.1093/jnci/85.6.488.
Hematopoietic growth factors (HGFs) have been shown to reduce the incidence of neutropenia and fever in patients receiving cancer chemotherapy.
This cost analysis was designed to determine the conditions in which use of HGFs in patients receiving cancer chemotherapy is cost-effective.
We used a standard model based on decision theory; the model assumes that all patients experiencing neutropenia and fever will be hospitalized and treated with intravenous antibiotics. Data from a prospective, randomized clinical trial of granulocyte colony-stimulating factor in small-cell lung cancer treated with combination chemotherapy were used to determine baseline probabilities for control hospitalization risk and survival; proportional hospitalization risk with prophylactic HGF; and median durations of hospitalization and prophylactic HGF use. The model was analyzed by one-way and multivariate sensitivity analyses, with estimation of threshold values at which the expected cost is the same for either of two treatment options. One or more of the specific costs and durations and the probability for each group of threshold curves were varied in a sensitivity analysis that generated variable thresholds. Use of Monte Carlo analysis based on the available distributions of the main variables provided 90% confidence limits and an inference method for comparing decision options.
The expected excess cost per treatment cycle, based on hospitalization for neutropenic fever and/or HGF administration, was $5500 for no HGF, $4750 for prophylactic HGF, and $6875 for therapeutic HGF. Sensitivity analysis provided the following thresholds for no HGF versus prophylactic HGF: control risk of hospitalization, 0.40; risk of hospitalization with HGF as a proportion of control, 0.64; total daily cost of hospitalization, $727; total daily cost of HGF, $344; duration of hospitalization, 7.3 days; and duration of HGF use, 11.0 days. Multivariate analysis revealed that conditions favoring the use of HGF on a cost basis become greater (a) as risk of hospitalization, total daily hospital cost, and duration of hospitalization increase and (b) as the proportional risk of hospitalization with HGF, daily cost of HGF, and duration of HGF treatment decrease.
The major determinants of total excess cost were the control risk of hospitalization, the proportional reduction in risk with HGF, and the average daily hospital cost.
Use of HGFs should be based on the risk of hospitalization for neutropenic fever and consideration of the patient population and institutional costs.
造血生长因子(HGFs)已被证明可降低接受癌症化疗患者的中性粒细胞减少症和发热的发生率。
本成本分析旨在确定在接受癌症化疗的患者中使用HGFs具有成本效益的条件。
我们使用了基于决策理论的标准模型;该模型假设所有发生中性粒细胞减少症和发热的患者都将住院并用静脉抗生素治疗。来自一项前瞻性、随机临床试验的数据,该试验对接受联合化疗的小细胞肺癌患者使用粒细胞集落刺激因子,用于确定控制住院风险和生存的基线概率;预防性使用HGF时的成比例住院风险;以及住院和预防性使用HGF的中位持续时间。通过单因素和多因素敏感性分析对模型进行分析,估计两个治疗方案中预期成本相同时的阈值。在敏感性分析中改变一个或多个特定成本、持续时间以及每组阈值曲线的概率,从而产生可变阈值。基于主要变量的可用分布进行蒙特卡罗分析,提供90%的置信区间和用于比较决策选项的推断方法。
基于中性粒细胞减少性发热住院和/或使用HGF,每个治疗周期的预期额外成本为:不使用HGF时为5500美元,预防性使用HGF时为4750美元,治疗性使用HGF时为6875美元。敏感性分析给出了不使用HGF与预防性使用HGF的以下阈值:控制住院风险为0.40;使用HGF时的住院风险相对于对照的比例为0.64;住院每日总成本为727美元;HGF每日总成本为344美元;住院持续时间为7.3天;以及使用HGF的持续时间为11.0天。多因素分析表明,在成本基础上有利于使用HGF的条件变得更加有利:(a)随着住院风险、住院每日总成本和住院持续时间增加;(b)随着使用HGF时的成比例住院风险、HGF每日成本和HGF治疗持续时间减少。
总额外成本的主要决定因素是控制住院风险、使用HGF时风险的成比例降低以及住院平均每日成本。
HGFs的使用应基于中性粒细胞减少性发热的住院风险,并考虑患者群体和机构成本。