Cost-utility analysis of pembrolizumab versus nivolumab in the treatment of metastatic colorectal cancer from the perspective of the healthcare payer.

IF 0.9 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Zhen Lu, Xiaoyan Huang, Yingjuan Ou, Qinbo Wang, Qirong Tan
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引用次数: 0

Abstract

Background: Colorectal cancer (CRC) is a malignant tumor with the third highest incidence worldwide. The comprehensive economic evaluation of programmed cell death protein-1 inhibitors in China, however, has not yet been carried out. The aim of this study is to assess the cost-utility of pembrolizumab and nivolumab in the treatment of metastatic colorectal cancer (mCRC).

Materials and methods: A Markov model microsimulation of efficacy and cost-utility analysis (CUA) was carried out, and efficacy and safety data were compared using network meta-analysis. Literature screening and data extraction were performed according to established criteria where the main outcome indicators, complete response (CR), partial response (PR), stable disease (SD), and progressive disease (PD) were compared between two treatments. The lifetime cost and outcomes of mCRC treatment were estimated, and quality-adjusted life years (-QALYs) and incremental cost-effectiveness ratio (ICER) were used to evaluate the economy of each program.

Results: A total of 442 studies were evaluated of which 15, with a total of 798 patients, were included in the analysis. Of these, 13 evaluated PD, and total patients for CR, PR, SD, and PD were 82, 283, 160, and 180 respectively. The corresponding heterogeneity values were (p = 0.13, heterogeneity index as percentage (I2) = 29.53%), (p < 0.01, I2 = 72.55%), (p = 0.03, I2 = 46.54%), (p < 0.01, I2 = 80.31%), and (p = 0.13 > 0.05). The proportion of patients classified as CR in the pembrolizumab group was greater than in the nivolumab group (0.105 vs. 0.085). However, the number of patients classified as PR and SD in the nivolumab group exceeded those in the pembrolizumab group. The number of patients classified as PD were similar in the two groups. Combination therapy nivolumab + ipilimumab yielded an incremental gain of 0.04 QALYs at an additional cost of 356,723 ¥. The ICER reached 8,918,075 ¥/QALYs, surpassing three times the per capita gross domestic product (GDP).

Conclusion: Both pembrolizumab and nivolumab showed beneficial effects in patients with mCRC. Nivolumab in combination with ipilimumab led to improved progression-free survival, but the values for ICER reached 8,918,075 ¥/QALYs. Treatment of non-resectable or metastatic microsatellite instability-high (MSI-H)/deficient mismatch repair (dMMR) advanced solid tumors CRC with pembrolizumab alone, in the Chinese population examined, was the most cost-effective, where the willingness-to-pay threshold was 242,928 ¥/QALY (100 ¥ = 13.75 US$ and 12.63 €).

从医疗保健支付者的角度分析派姆单抗与纳武单抗治疗转移性结直肠癌的成本效用。
背景:结直肠癌(Colorectal cancer, CRC)是全球发病率第三高的恶性肿瘤。然而,中国尚未对程序性细胞死亡蛋白-1抑制剂进行全面的经济评估。本研究的目的是评估派姆单抗和纳武单抗治疗转移性结直肠癌(mCRC)的成本-效用。材料和方法:采用马尔科夫模型进行疗效和成本效用分析(CUA)微观模拟,并采用网络meta分析对疗效和安全性数据进行比较。根据建立的标准进行文献筛选和数据提取,比较两种治疗的主要结局指标,完全缓解(CR)、部分缓解(PR)、疾病稳定(SD)和疾病进展(PD)。评估mCRC治疗的终生成本和结局,并使用质量调整生命年(-QALYs)和增量成本-效果比(ICER)来评估每个方案的经济性。结果:共评估了442项研究,其中15项共798例患者被纳入分析。其中13例评估PD, CR、PR、SD和PD患者总数分别为82例、283例、160例和180例。相应的异质性值分别为(p = 0.13,异质性指数百分比(I2) = 29.53%)、(p < 0.01, I2 = 72.55%)、(p = 0.03, I2 = 46.54%)、(p < 0.01, I2 = 80.31%)和(p = 0.13 bb0 0.05)。派姆单抗组CR患者比例大于纳武单抗组(0.105 vs 0.085)。然而,在纳武单抗组中,归类为PR和SD的患者数量超过了派姆单抗组。两组PD患者数量相近。联合治疗nivolumab + ipilimumab获得0.04 QALYs的增量收益,额外成本为356,723日元。ICER达到8,918,075元/QALYs,超过人均国内生产总值(GDP)的三倍。结论:派姆单抗和纳武单抗对mCRC患者均有有益效果。Nivolumab联合ipilimumab可改善无进展生存期,但ICER值达到8,918,075¥/QALYs。在中国人群中,单独使用pembrolizumab治疗不可切除或转移性微卫星不稳定性高(MSI-H)/缺陷错配修复(dMMR)晚期实体肿瘤CRC是最具成本效益的,其支付意愿阈值为242,928元/QALY(100元= 13.75美元和12.63欧元)。
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
1.70
自引率
12.50%
发文量
116
审稿时长
4-8 weeks
期刊介绍: The International Journal of Clinical Pharmacology and Therapeutics appears monthly and publishes manuscripts containing original material with emphasis on the following topics: Clinical trials, Pharmacoepidemiology - Pharmacovigilance, Pharmacodynamics, Drug disposition and Pharmacokinetics, Quality assurance, Pharmacogenetics, Biotechnological drugs such as cytokines and recombinant antibiotics. Case reports on adverse reactions are also of interest.
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