Zheng Zhiwei, Zhu Huide, Fang Ling
Department of Pharmacy, Cancer Hospital of Shantou University Medical College, Shantou, China.
PLoS One. 2025 Mar 25;20(3):e0320189. doi: 10.1371/journal.pone.0320189. eCollection 2025.
This study aims to conduct a cost-effectiveness analysis of tislelizumab in combination with platinum and etoposide compared to the standard treatment of etoposide and platinum as first-line therapy for extensive-stage small cell lung cancer(ES-SCLC) from the Chinese medical system perspective.
A partitioned survival model was developed utilizing data from the RATIONALE-312 trial to accurately simulate the clinical and economic outcomes of both treatment arms. This model incorporates three distinct health states, namely progression-free survival, disease progression, and death. These states are exclusive of each other, and patients can transition between them as their disease progresses.The model accounted for various cost components such as drug therapy, management of adverse events, disease progression, and overall survival. To evaluate the cost-effectiveness of the interventions, quality-adjusted life-year (QALY) and incremental cost-effectiveness ratio (ICER) were chosen as the metrics. The analysis employed a willingness to pay (WTP) threshold of $39,855.79 per QALY. Additionally, sensitivity analyses were conducted to assess the robustness and reliability of the model.
The tislelizumab group had a total cost of $52,749.69, whereas the chemotherapy group's total expenses amounted to $8,811.62. Additionally, the tislelizumab group experienced a gain of 2.21 QALY compared to the chemotherapy group, albeit incurring an additional cost of $43,938.07. Consequently, this led to an ICER of $19,881.48, which falls below the Chinese WTP threshold of $39,855.79. Sensitivity analyses confirmed the robustness of the findings across a range of scenarios.
This cost-effectiveness analysis based on the RATIONALE-312 trial demonstrates that tislelizumab plus platinum and etoposide is a cost-effective treatment option for ES-SCLC compared to the standard chemotherapy from the Chinese medical system perspective.
本研究旨在从中国医疗体系的角度,对替雷利珠单抗联合铂类和依托泊苷与依托泊苷和铂类的标准治疗作为广泛期小细胞肺癌(ES-SCLC)一线治疗方案进行成本效益分析。
利用RATIONALE-312试验的数据建立了一个分区生存模型,以准确模拟两个治疗组的临床和经济结果。该模型包含三个不同的健康状态,即无进展生存期、疾病进展期和死亡。这些状态相互排斥,患者会随着疾病进展在它们之间转换。该模型考虑了各种成本组成部分,如药物治疗、不良事件管理、疾病进展和总生存期。为了评估干预措施的成本效益,选择了质量调整生命年(QALY)和增量成本效益比(ICER)作为指标。分析采用的支付意愿(WTP)阈值为每QALY 39,855.79美元。此外,还进行了敏感性分析,以评估模型的稳健性和可靠性。
替雷利珠单抗组的总成本为52,749.69美元,而化疗组的总费用为8,811.62美元。此外,与化疗组相比,替雷利珠单抗组的QALY增加了2.21个,尽管额外增加了43,938.07美元的成本。因此,这导致ICER为19,881.48美元,低于中国的WTP阈值39,855.79美元。敏感性分析证实了在一系列情景下研究结果的稳健性。
基于RATIONALE-312试验的这项成本效益分析表明,从中国医疗体系的角度来看,与标准化疗相比,替雷利珠单抗联合铂类和依托泊苷是ES-SCLC的一种具有成本效益的治疗选择。