Department of Pharmacy, Nanxishan Hospital of Guangxi Zhuang Autonomous Region, Guilin, China.
Department of Oncology, Nanxishan Hospital of Guangxi Zhuang Autonomous Region, Guilin, China.
Int J Clin Pharm. 2024 Dec;46(6):1536-1545. doi: 10.1007/s11096-024-01802-1. Epub 2024 Sep 14.
Tislelizumab combined with chemotherapy has shown significant clinical benefits in improving overall survival compared to chemotherapy alone for patients with extensive-stage small-cell lung cancer (ES-SCLC).
This study aimed to evaluate the cost-effectiveness of tislelizumab plus chemotherapy versus standard chemotherapy as a first-line treatment for ES-SCLC from the US payer perspective and the perspective of the Chinese healthcare system.
We conducted an economic evaluation using a Markov state-transition model, reflecting the US payer perspective and the perspective of the Chinese healthcare system. Baseline patient characteristics and essential clinical data were obtained from the RATIONALE-312 trial. The costs and utilities were derived from open-access databases and published literature. The primary outcomes measured included quality-adjusted life years (QALYs), incremental cost-effectiveness ratio (ICER), incremental net health benefit (INHB), and incremental net monetary benefit (INMB). Uncertainties in the model were addressed by probabilistic sensitivity analysis (PSA) and one-way sensitivity analysis (OWSA).
In the base-case analysis, the addition of tislelizumab to chemotherapy provided an incremental gain of 0.16 QALYs at an additional cost of $7430.73, resulting in an ICER of $46,132.33 per QALY. Although above the willingness-to-pay (WTP) threshold of China of $38,042.49 per QALY, the cost-effectiveness was marginal, with an INHB of - 0.03 QALYs and an INMB of $- 1303.06. In the US, despite a slightly higher effectiveness gain of 0.28 QALYs, the increased cost of $45,157.35 resulted in an unfavorable ICER of $163,885.06 per QALY, exceeding the US WTP threshold of $150,000.00. PSA showed probabilities of cost-effectiveness of tislelizumab plus chemotherapy at 17.18% in China and 40.41% in the US.
Tislelizumab combined with chemotherapy was not a cost-effective first-line treatment option for ES-SCLC in China or the US; however, the margin of cost-effectiveness was narrow.
替雷利珠单抗联合化疗与单纯化疗相比,可显著改善广泛期小细胞肺癌(ES-SCLC)患者的总生存期,具有显著的临床获益。
本研究旨在从美国支付者和中国医保视角评估替雷利珠单抗联合化疗对比标准化疗作为 ES-SCLC 一线治疗的成本-效果。
我们采用 Markov 状态转移模型进行经济评价,反映了美国支付者和中国医保视角。患者基线特征和关键临床数据来自 RATIONALE-312 试验。成本和效用值来自公开数据库和已发表的文献。主要结局指标包括质量调整生命年(QALYs)、增量成本效果比(ICER)、增量净健康收益(INHB)和增量净货币收益(INMB)。模型中的不确定性通过概率敏感性分析(PSA)和单因素敏感性分析(OWSA)进行处理。
在基础分析中,替雷利珠单抗联合化疗可使 QALY 增加 0.16,成本增加 7430.73 美元,ICER 为 46132.33 美元/QALY。尽管高于中国 38042.49 美元/QALY 的意愿支付阈值,但成本效果较为边缘,INHB 为-0.03 QALY,INMB 为-1303.06 美元。在美国,尽管疗效提高了 0.28 QALY,但增加的 45157.35 美元成本导致 ICER 为 163885.06 美元/QALY,超过了美国 150000.00 美元的意愿支付阈值。PSA 显示替雷利珠单抗联合化疗在中国的成本效果概率为 17.18%,在美国为 40.41%。
替雷利珠单抗联合化疗在中国或美国均不是 ES-SCLC 的一种具有成本效果的一线治疗选择,但是成本效果的边缘很窄。