Comparative clinical and economic analysis of using cabozantinib as second-line therapy for adult patients with advanced renal cell carcinoma

IF 0.1 Q4 ONCOLOGY
I. Krysanov, V. Krysanova, B. Alekseev, V. Ermakova, E. Gameeva
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引用次数: 0

Abstract

Background. Currently there exists a wide range of advanced renal cell carcinoma (RCC) treatment schemes, among them cabozantinib, registered in Russia in 2019, was approved as a second-line therapy in both foreign and domestic guidelines. Objective: to conduct a comparative clinical and economic analysis of cabozantinib and alternative drugs in adult patients with advanced RCC after previous systemic therapy. Materials and methods. A literature review was conducted on clinical efficacy and safety of various second-line therapy drugs for advanced RCC in the available databases. The foreign partitioned survival model, reflecting the development of widespread RCC when using 4 different second-line therapy drugs (cabosantinib, nivolumab, axitinib and everolimus), was adapted considering 3 consecutive mutually exclusive conditions (before progression, after progression, death). Pharmacoeconomic analysis included “cost-effectiveness” and “cost-utility” analysis. We estimated direct medical costs for second- and third-line therapy and maintenance therapy (outpatient monitoring and palliative care). To estimate drug costs we used prices from the State Register of maximum selling prices, for cabozanthinib — price presented by the manufacturer. Costs of maintenance therapy were estimated based on the normal standardfor financial costs in accordance with the Program of state guarantees for 2020. Results. Efficacy analysis based on the partitioned survival model showed the highest rates of life-years gained (3.18 life-years-gained (LYG)) and quality adjusted life-years (1.87quality adjusted life-years (QALY)) for cabozanthinib compared with nivolumab (2.53 LYG and 1.6 QALY), axitinib and everolimus (2.21 LYG and 1.31 QALY). Total costs for advanced RCC patients when treated with cabozanthinib were 4.3 million rubles, which is 5 % less than when using nivolumab (4.5 million rubles). Total costs for axitinib were 2.1 million rubles, while its effectiveness was lower compared with the cabozanthinib one. Costs of 1 life-year saved for cabozantinib were 1.4 million rubles, which is 25 % less compared to those for nivolumab. Costs of 1 quality-life year saved when using cabozantinib amounted 2.3 million rubles, which is 19 % less than those for nivolumab. Conclusion. The study results showed that using cabozantinib to treat advanced RCC after previous systemic treatment is both clinically and cost-effective for adult patients with advanced RCC in the Russian Federation.
卡博赞替尼作为成人晚期肾细胞癌二线治疗的比较临床和经济分析
背景。目前存在多种晚期肾细胞癌(RCC)治疗方案,其中2019年在俄罗斯注册的卡博赞替尼(cabozantinib)在国内外指南中均被批准为二线治疗药物。目的:对成人晚期RCC患者既往全身治疗后,卡博赞替尼与替代药物进行临床和经济对比分析。材料和方法。对现有数据库中各种二线治疗药物治疗晚期肾癌的临床疗效和安全性进行文献综述。国外的分割生存模型反映了在使用4种不同的二线治疗药物(卡博桑替尼、纳武单抗、阿西替尼和依维莫司)时广泛的RCC的发展,该模型考虑了3个连续的相互排斥的条件(进展前、进展后、死亡)。药物经济学分析包括“成本-效果”分析和“成本-效用”分析。我们估计了二线和三线治疗和维持治疗(门诊监测和姑息治疗)的直接医疗费用。为了估计药物成本,我们使用了卡博赞替尼的最高销售价格——生产商提供的价格——国家注册表中的价格。根据2020年国家保障计划,按照正常的财务费用标准估算维持治疗费用。结果。基于分区生存模型的疗效分析显示,与纳沃单抗(2.53 LYG和1.6 QALY)、阿西替尼和依维莫司(2.21 LYG和1.31 QALY)相比,卡博赞替尼获得的生命年(3.18生命年)和质量调整生命年(1.87质量调整生命年)的比率最高。使用卡博赞替尼治疗晚期RCC患者的总费用为430万卢布,比使用纳武单抗(450万卢布)低5%。阿西替尼的总成本为210万卢布,而其有效性低于卡博赞替尼。卡博赞替尼节省1个生命年的成本为140万卢布,与纳武单抗相比减少了25%。使用卡博赞替尼节省1个质量生命年的成本为230万卢布,比使用纳武单抗节省19%。结论。研究结果表明,对于俄罗斯联邦成年晚期RCC患者,在既往全身治疗后再使用卡博赞替尼治疗晚期RCC具有临床和成本效益。
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来源期刊
Onkourologiya
Onkourologiya ONCOLOGY-
CiteScore
0.40
自引率
0.00%
发文量
59
审稿时长
10 weeks
期刊介绍: The main objective of the journal "Cancer urology" is publishing up-to-date information about scientific clinical researches, diagnostics, treatment of oncologic urological diseases. The aim of the edition is to inform the experts on oncologic urology about achievements in this area, to build understanding of the necessary integrated interdisciplinary approach in therapy, alongside with urologists, combining efforts of doctors of various specialties (cardiologists, pediatricians, chemotherapeutists et al.), to contribute to raising the effectiveness of oncologic patients’ treatment.
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