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TAS-102联合或不联合贝伐单抗治疗转移性结直肠癌患者:一项多国成本效益分析。

TAS-102 with or without bevacizumab treatment for patients with metastatic colorectal cancer: a multi-country cost-effectiveness analysis.

作者信息

Zhu Youwen, Liu Kun, Zhu Hong

机构信息

Department of Oncology, Xiangya Hospital, Central South University, Changsha, Hunan, China.

Department of Oncology, Xiangya Hospital, Central South University, No. 87 Xiangya North Road, Changsha, Hunan 410008, China National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, Hunan, China.

出版信息

Therap Adv Gastroenterol. 2024 Sep 28;17:17562848241284998. doi: 10.1177/17562848241284998. eCollection 2024.

Abstract

BACKGROUND

TAS-102 (trifluridine/tipiracil) plus bevacizumab demonstrated a significant survival benefit in patients with refractory metastatic colorectal cancer (mCRC). Physicians and patients are uncertain whether this treatment option is clinically acceptable in different countries, underscoring the need for analyses of the cost-effectiveness of this regimen.

OBJECTIVES

To guide doctors and patients to choose TAS-102 plus bevacizumab or TAS-102 monotherapy in cancer treatment.

DESIGN

The cost-effective analysis.

METHODS

A comprehensive Markov model of the 10-year horizon for three health states was established using data from the SUNLIGHT trial to evaluate the cost and health effects of TAS-102 with or without bevacizumab at particular willingness-to-pay (WTP) thresholds, analyzing parameters including quality-adjusted life-years (QALYs), incremental cost-effectiveness ratios (ICERs), incremental net monetary benefit, as well as incremental net-health benefit (INHB). Sensitivity and subgroup analyses were additionally conducted.

RESULTS

Treatment with TAS-102 plus bevacizumab versus TAS-102 monotherapy increased effectiveness (cost) by 0.39 ($151,474), 0.38 ($26,794), and 0.41 ($8596) QALYs, with an ICER of $388,171, $69,617, and $20,919 per QALY and an INHB of -0.62, -0.03, and 0.18 QALYs in the United States, United Kingdom, and China, respectively. The utility of progression-free survival was the most important factor in this model. At respective WTP thresholds of $150,000, $65,000, and $37,653 per QALY in the United States, United Kingdom, and China, the odds of TAS-102 plus bevacizumab being the dominant treatment were 0%, 49.6%, and 87.8%, respectively. In addition, mCRC patients with an Eastern Oncology Cooperative Group performance status ⩾ 1 may be the best candidates for treatment.

CONCLUSION

TAS-102 plus bevacizumab treatment represents a cost-effective third-line treatment for refractory mCRC from a Chinese payers' perspective, although the same was not true in the United States or United Kingdom at current drug prices.

摘要

背景

TAS-102(曲氟尿苷/替匹嘧啶)联合贝伐单抗在难治性转移性结直肠癌(mCRC)患者中显示出显著的生存获益。医生和患者不确定这种治疗方案在不同国家是否在临床上可接受,这突出了对该方案成本效益分析的必要性。

目的

指导医生和患者在癌症治疗中选择TAS-102联合贝伐单抗或TAS-102单药治疗。

设计

成本效益分析。

方法

利用SUNLIGHT试验的数据建立了一个为期10年、包含三种健康状态的综合马尔可夫模型,以评估在特定支付意愿(WTP)阈值下,使用或不使用贝伐单抗的TAS-102的成本和健康效果,分析参数包括质量调整生命年(QALY)、增量成本效益比(ICER)、增量净货币效益以及增量净健康效益(INHB)。此外还进行了敏感性和亚组分析。

结果

在美国、英国和中国,TAS-102联合贝伐单抗治疗与TAS-102单药治疗相比,有效性(成本)分别增加了0.39(151,474美元)、0.38(26,794美元)和0.41(8596美元)个QALY,ICER分别为每QALY 388,171美元、69,617美元和20,919美元,INHB分别为-0.62、-0.03和0.18个QALY。无进展生存的效用是该模型中最重要的因素。在美国、英国和中国,每QALY的WTP阈值分别为150,000美元、65,000美元和37,653美元时,TAS-102联合贝伐单抗成为主要治疗方案的概率分别为0%、49.6%和87.8%。此外,东部肿瘤协作组体能状态⩾1的mCRC患者可能是最佳治疗候选者。

结论

从中国支付方的角度来看,TAS-102联合贝伐单抗治疗代表了一种针对难治性mCRC具有成本效益的三线治疗方案,尽管按照当前药品价格,在美国和英国并非如此。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5417/11450621/6f24f3bfe2ed/10.1177_17562848241284998-fig1.jpg

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