Comparative clinical and economic assessment of polatuzumab vedotin therapy in combination with bendamustine and rituximab for adult transplantation-ineligible patients with relapsed/refractory diffuse large B-cell lymphoma

Q4 Medicine
I. Dyakov, K. K. Bushkova
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引用次数: 0

Abstract

Aim. To evaluate the pharmacoeconomic feasibility of using polatuzumab vedotin in combination with bendamustine and rituximab for the treatment of adult transplantation-ineligible patients with relapsed/refractory diffuse large B-cell lymphoma.Materials and methods. Study design - retrospective analysis of literature data. Pharmacoeconomic research methods - clinical and economic analysis (incremental cost-effectiveness analysis, case-based approach) using sensitivity assessment. The sources of the drug efficacy data were publications on conducted clinical trials; on the drugs cost -the State register of maximum selling prices, data from the manufacturer's company.Results. Polatuzumab vedotin is the unique drug from the class of monoclonal antibody-antimitotic agent conjugates registered in Russia for the treatment of adult transplantation-ineligible patients with relapsed/refractory diffuse large B-cell lymphoma. for this reason a case-based approach was applied as part of the cost-effectiveness analysis. As a result of clinical and economic analysis, it was found that the cost of progression free life-year added when using polatuzumab vedotin in combination with bendamustine and rituximab in patients with relapsed/refractory diffuse large b-cell lymphoma by 50.7 %, or by 11.4 million rubles, lower than the cost of progression free life-year added when using brentuximab vedotin in patients with relapsed/refractory Hodgkin's lymphoma. The sensitivity assessment showed the stability of the obtained results to changes in the input parameters of treatment cost and efficacy in a wide range of values.Conclusion. Use of polatuzumab vedotin in combination with bendamustine and rituximab for the treatment of adult transplantation-ineligible patients with diffuse large B-cell non-Hodgkin's lymphoma is pharmacoeconomically justified and appropriate. 
polatuzumab vedotin联合苯达莫司汀和利妥昔单抗治疗复发/难治性弥漫性大b细胞淋巴瘤成人不适合移植患者的比较临床和经济评估
的目标。评估polatuzumab vedotin联合苯达莫司汀和利妥昔单抗治疗复发/难治性弥漫性大b细胞淋巴瘤成人不适合移植患者的药物经济学可行性。材料和方法。研究设计-文献资料回顾性分析。药物经济学研究方法-使用敏感性评估的临床和经济分析(增量成本效益分析,基于病例的方法)。药物疗效数据的来源是已进行的临床试验的出版物;关于药品成本——国家最高销售价格注册表,来自制造商公司的数据。Polatuzumab vedotin是俄罗斯注册的单克隆抗体-抗核分裂药物偶联物类中唯一的药物,用于治疗复发/难治性弥漫性大b细胞淋巴瘤的成人不适合移植患者。因此,采用了基于案例的方法作为成本效益分析的一部分。临床和经济分析的结果发现,在复发/难治性弥漫性大b细胞淋巴瘤患者中使用polatuzumab vedotin联合苯达莫司汀和利妥昔单抗时,增加的无进展生命年成本为50.7%,或1140万卢布,低于在复发/难治性霍奇金淋巴瘤患者中使用brentuximab vedotin时增加的无进展生命年成本。敏感性评价表明,所得结果在较宽范围内对治疗费用和疗效输入参数的变化具有稳定性。使用polatuzumab vedotin联合苯达莫司汀和利妥昔单抗治疗不适合移植的成人弥漫性大b细胞非霍奇金淋巴瘤患者在药物经济学上是合理和适当的。
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来源期刊
CiteScore
0.80
自引率
0.00%
发文量
20
审稿时长
12 weeks
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