Cost-effectiveness of socazolimab plus chemotherapy vs. standard chemotherapy for first-line treatment of extensive-stage small cell lung cancer: a U.S. and China perspective.

IF 2.5 3区 医学 Q2 ONCOLOGY
Wenwang Lang, Jiangbo Wang, Haiqing Zhao, Yulong He, Qinling Jiang, Qi Ai, Ming Ouyang
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引用次数: 0

Abstract

Purpose: Socazolimab, in combination with chemotherapy, has been shown to prolong progression-free survival (PFS) and overall survival (OS) compared with chemotherapy alone in patients with extensive-stage small cell lung cancer (ES-SCLC). This study is the first to evaluate its cost-effectiveness from the perspectives of both the U.S. payer and Chinese healthcare systems.

Methods: A Markov state-transition model was employed to conduct an economic evaluation, incorporating clinical and economic parameters from both the U.S. and China. Baseline patient characteristics and key clinical inputs were sourced from a randomized phase 3 trial, whereas cost and utility values were derived from open-access databases and published literature. The primary outcomes assessed included quality-adjusted life-years (QALYs), incremental cost-effectiveness ratio (ICER), incremental net health benefit (INHB), and incremental net monetary benefit (INMB). Model uncertainty was addressed through probabilistic sensitivity, one-way sensitivity, and scenario analyses.

Results: In the base-case scenario, the addition of socazolimab to chemotherapy resulted in a marginal QALY gain of 0.09, at an incremental cost of $14,504.53, leading to an ICER of $152,228.60 per QALY. This ICER was below China's willingness-to-pay (WTP) threshold of $40,354.27 per QALY, making it not cost-effective, with an INHB of -0.26 QALYs and an INMB of -$10,523.93. In the U.S., while the incremental QALY gain remained at 0.10, the additional cost increased to $85,599.55, yielding an ICER of $878,912.80 per QALY, far exceeding that of the U.S. WTP threshold of $150,000.00, confirming its lack of cost-effectiveness.

Conclusions: The combination of socazolimab with chemotherapy is not a cost-effective first-line treatment option for ES-SCLC in either China or the United States, highlighting the need for price adjustments and alternative treatment strategies to improve economic viability.

索卡唑单抗联合化疗与标准化疗在一线广泛期小细胞肺癌治疗中的成本效益:美国和中国的视角
目的:与单纯化疗相比,索卡唑单抗联合化疗可延长广泛期小细胞肺癌(ES-SCLC)患者的无进展生存期(PFS)和总生存期(OS)。本研究首次从美国付款人和中国医疗保健系统的角度评估其成本效益。方法:采用马尔可夫状态转换模型,结合美国和中国的临床和经济参数进行经济评估。基线患者特征和关键临床输入来自随机3期试验,而成本和效用值来自开放获取数据库和已发表的文献。评估的主要结局包括质量调整生命年(QALYs)、增量成本-效果比(ICER)、增量净健康效益(INHB)和增量净货币效益(INMB)。模型的不确定性通过概率敏感性、单向敏感性和情景分析来解决。结果:在基本情况下,化疗中加入索卡唑单抗导致边际QALY增加0.09,增量成本为14,504.53美元,导致每个QALY的ICER为152,228.60美元。该ICER低于中国的支付意愿(WTP)门槛40,354.27美元/ QALY,使得其不具有成本效益,INHB为-0.26 QALY, INMB为- 10,523.93美元。在美国,虽然QALY增量收益保持在0.10,但额外成本增加到85,599.55美元,每个QALY的ICER为878,912.80美元,远远超过美国WTP门槛150,000.00美元,证实其缺乏成本效益。结论:无论在中国还是美国,索卡唑单抗联合化疗都不是ES-SCLC的一种具有成本效益的一线治疗选择,这突出了价格调整和替代治疗策略的必要性,以提高经济可行性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.20
自引率
2.90%
发文量
240
审稿时长
1 months
期刊介绍: Clinical and Translational Oncology is an international journal devoted to fostering interaction between experimental and clinical oncology. It covers all aspects of research on cancer, from the more basic discoveries dealing with both cell and molecular biology of tumour cells, to the most advanced clinical assays of conventional and new drugs. In addition, the journal has a strong commitment to facilitating the transfer of knowledge from the basic laboratory to the clinical practice, with the publication of educational series devoted to closing the gap between molecular and clinical oncologists. Molecular biology of tumours, identification of new targets for cancer therapy, and new technologies for research and treatment of cancer are the major themes covered by the educational series. Full research articles on a broad spectrum of subjects, including the molecular and cellular bases of disease, aetiology, pathophysiology, pathology, epidemiology, clinical features, and the diagnosis, prognosis and treatment of cancer, will be considered for publication.
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