Department of Clinical Pharmacy and Healthcare Science, Faculty of Pharmacy, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa University, Kanazawa, 920-1192, Japan.
Comprehensive Unit for Health Economic Evidence Review and Decision Support (CHEERS), Research Organization of Science and Technology, Ritsumeikan University, Kyoto city, Kyoto, Japan.
Clin Drug Investig. 2024 Oct;44(10):749-759. doi: 10.1007/s40261-024-01383-x. Epub 2024 Sep 21.
BACKGROUND AND OBJECTIVE: Recent trials have shown that immune checkpoint inhibitors (ICIs), atezolizumab and durvalumab, in combination with chemotherapy, are effective in treating extensive-disease small-cell lung cancer (ED-SCLC). However, owing to the expensiveness of ICIs, monetary issues arise. The cost-effectiveness of ICI combination treatment with carboplatin plus etoposide (CE) as first-line therapy for patients with ED-SCLC was examined to aid public health policy in Japan.
IMpower 133 and CASPIAN data were used to create a partitioned survival model. Medical expenses and quality-adjusted life years (QALYs) were considered. The analysis period, discount rate, and threshold were set at 20 years, 2%, and 15 million Japanese yen (JPY) [114,068 US dollars (USD)] per QALY, respectively. The incremental cost-effectiveness ratio (ICER) was calculated by gathering reasonable parameters from published reports and combining the costs and effects using parametric models. Monte Carlo simulations, scenario analysis, and one-way sensitivity analyses were employed to quantify uncertainty.
After comparing atezolizumab plus CE (ACE) and durvalumab plus CE (DCE) with CE, it was found that the ICERs exceeded the threshold at 35,048,299 JPY (266,527 USD) and 36,665,583 JPY (278,826 USD) per QALY, respectively. For one-way sensitivity and scenario assessments, the ICERs exceeded the threshold, even with considerably adjusted parameters. For the probabilistic sensitivity analyses, there was no probability that the ICER of the ICI combination treatment with chemotherapy would fall below the threshold.
ACE and DCE were not cost-effective compared with CE as first-line therapy for ED-SCLC in Japan. Both these therapies exhibited high ICERs.
最近的试验表明,免疫检查点抑制剂(ICI)阿替利珠单抗和度伐利尤单抗联合化疗治疗广泛期小细胞肺癌(ED-SCLC)有效。然而,由于 ICI 昂贵,会出现经济问题。本研究旨在评估 ICI 联合卡铂加依托泊苷(CE)作为 ED-SCLC 一线治疗的成本效益,以辅助日本的公共卫生政策。
使用 IMpower 133 和 CASPIAN 数据构建分区生存模型。考虑医疗费用和质量调整生命年(QALY)。分析期、贴现率和阈值分别设定为 20 年、2%和 1500 万日元(JPY)[114068 美元(USD)]每 QALY。通过从已发表的报告中收集合理的参数并使用参数模型对成本和效果进行组合,计算增量成本效益比(ICER)。采用蒙特卡罗模拟、情景分析和单向敏感性分析来量化不确定性。
与 CE 相比,阿替利珠单抗联合 CE(ACE)和度伐利尤单抗联合 CE(DCE)的 ICER 分别为 35048299 日元(266527 美元)和 36665583 日元(278826 美元),均超过了阈值。对于单向敏感性和情景评估,即使参数调整幅度较大,ICER 仍超过了阈值。对于概率敏感性分析,ICI 联合化疗治疗的 ICER 低于阈值的概率为零。
ACE 和 DCE 作为日本 ED-SCLC 的一线治疗,与 CE 相比均不具有成本效益。这两种治疗方法的 ICER 均较高。