Key Specialty of Clinical Pharmacy, The First Affiliated Hospital of Guangdong Pharmaceutical University, Guangzhou, China.
Front Public Health. 2024 Nov 13;12:1465898. doi: 10.3389/fpubh.2024.1465898. eCollection 2024.
The combination of trifluridine/tipiracil (FTD/TPI) and bevacizumab has demonstrated promising efficacy and safety in the treatment of colorectal cancer (CRC). This study aims to evaluate the cost-effectiveness of trifluridine/tipiracil combined with bevacizumab vs. trifluridine/tipiracil monotherapy as a third-line treatment regimen for colorectal cancer within the Chinese healthcare system, providing an economic basis for clinical application.
Based on data from the SUNLIGHT Phase III clinical trial, a dynamic Markov model was constructed with a cycle length of 4 weeks and a simulation duration of 10 years. Direct medical costs and quality-adjusted life years (QALYs) were calculated. The incremental cost-effectiveness ratio (ICER) was compared with the willingness-to-pay threshold (WTP = ¥268,200.00/QALY) to assess the economic viability of the treatment regimen. One-way sensitivity analysis and probabilistic sensitivity analysis were conducted to verify the robustness of the model results.
The cost of trifluridine/tipiracil combined with bevacizumab treatment (¥838,492.74) was higher than that of trifluridine/tipiracil monotherapy (¥357,396.97), with greater health benefits (2.45 QALYs vs. 1.54 QALYs). The ICER was ¥527,577.36/QALY, exceeding the willingness-to-pay threshold. One-way sensitivity analysis indicated that drug costs and utility values during the progression-free period significantly impacted model outputs. Probabilistic sensitivity analysis further confirmed the robustness of the results, showing that at a willingness-to-pay threshold of ¥494,000.00, the probability of the combined treatment being cost-effective was 50%.
Trifluridine/tipiracil combined with bevacizumab, as a third-line treatment for colorectal cancer, does not have a cost-effectiveness advantage compared to trifluridine/tipiracil monotherapy in economic evaluations.
替氟尿苷/盐酸拓扑替康(FTD/TPI)联合贝伐珠单抗在治疗结直肠癌(CRC)方面显示出了令人鼓舞的疗效和安全性。本研究旨在评估替氟尿苷/盐酸拓扑替康联合贝伐珠单抗对比替氟尿苷/盐酸拓扑替康单药作为三线治疗方案用于中国医疗体系下结直肠癌的成本效果,为临床应用提供经济学依据。
基于 SUNLIGHT 三期临床试验数据,构建了一个周期长度为 4 周、模拟时间为 10 年的动态 Markov 模型。计算了直接医疗成本和质量调整生命年(QALY)。采用增量成本效果比(ICER)与意愿支付阈值(WTP=¥268200.00/QALY)进行比较,以评估治疗方案的经济性。进行了单因素敏感性分析和概率敏感性分析,以验证模型结果的稳健性。
替氟尿苷/盐酸拓扑替康联合贝伐珠单抗治疗的成本(¥838492.74)高于替氟尿苷/盐酸拓扑替康单药治疗(¥357396.97),但健康获益更大(2.45 QALY 对比 1.54 QALY)。ICER 为 ¥527577.36/QALY,超过了意愿支付阈值。单因素敏感性分析表明,无进展生存期的药物成本和效用值对模型结果有显著影响。概率敏感性分析进一步证实了结果的稳健性,显示在意愿支付阈值为 ¥494000.00 时,联合治疗具有成本效果的概率为 50%。
在经济评价中,与替氟尿苷/盐酸拓扑替康单药相比,替氟尿苷/盐酸拓扑替康联合贝伐珠单抗作为结直肠癌三线治疗方案不具有成本效果优势。