Costs of Treating Onasemnogene Abeparvovec-Xioi-Induced Liver Injury.

IF 2.3 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Andrej Belančić, Branislava Raičević, Ivana Stević, Dinko Vitezić, Slobodan M Janković
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Abstract

Aims were to reveal types of onasemnogene abeparvovec-xioi (OA)-induced liver injury, their treatment patterns, utilization of healthcare, and treatment costs. This study employed secondary research to analyze OA-induced liver injury using data from the EudraVigilance database, published case reports, cohort studies, and clinical trials. The extracted data were analyzed to define real-life clinical entities that could be clearly outlined as syndromes resulting from the OA-induced liver injury, and further used in guiding the development of healthcare utilization matrices. Serbian healthcare costs were calculated by multiplying utilization figures by local unit prices, converted to Euros using exchange rates and adjusted by price level indices. A spreadsheet model with uniform distributions simulated costs for 1000 virtual patients, providing mean values and standard deviations for Serbia and the EU. From 1566 adverse event reports in the EudraVigilance database following OA therapy, 231 were hepatobiliary disorders, predominantly hypertransaminasaemia (30.7%; 71/231). Liver injury largely manifested as mild-to-moderate biochemical abnormalities, rarely progressing to severe complications, and was effectively managed with corticosteroid therapy. Economic analysis highlights the manageable burden of OA-induced liver injury. In the EU, mild-to-moderate cases cost €823.7, while severe cases average €1638.6. Medication costs range from €26.8 for prednisone to €695.4 for severe cases requiring additional immunosuppressive agents like tacrolimus and mycophenolate mofetil. To conclude, OA-induced liver injury, though notable, is clinically manageable with immunosuppressive therapy and rarely causes severe complications like encephalopathy or liver failure. Its modest costs do not undermine OA's cost-effectiveness, supporting its transformative role in spinal muscular atrophy treatment.

治疗Onasemnogene abparvovec - xii诱导的肝损伤的费用。
目的是揭示onasemnogene abparvovec -xioi (OA)诱导的肝损伤类型、治疗模式、医疗保健利用和治疗费用。本研究采用二次研究方法,利用EudraVigilance数据库、已发表病例报告、队列研究和临床试验的数据,分析oa诱导的肝损伤。对提取的数据进行分析,以定义现实生活中的临床实体,这些实体可以明确地概括为由oa引起的肝损伤引起的综合征,并进一步用于指导医疗保健利用矩阵的开发。塞尔维亚保健费用的计算方法是利用数字乘以当地单位价格,用汇率换算成欧元,并按价格水平指数进行调整。一个具有均匀分布的电子表格模型模拟了1000名虚拟患者的成本,提供了塞尔维亚和欧盟的平均值和标准差。在EudraVigilance数据库中,OA治疗后的1566例不良事件报告中,231例为肝胆功能障碍,主要是高转氨酶血症(30.7%;71/231)。肝损伤主要表现为轻度至中度生化异常,很少进展为严重并发症,并通过皮质类固醇治疗有效管理。经济分析强调,oa引起的肝损伤负担是可控的。在欧盟,轻中度病例的费用为823.7欧元,而重度病例的平均费用为1638.6欧元。药物费用从强的松的26.8欧元到需要使用他克莫司和霉酚酸酯等额外免疫抑制剂的重症患者的695.4欧元不等。综上所述,oa引起的肝损伤虽然值得注意,但在临床上通过免疫抑制治疗是可以控制的,并且很少引起脑病或肝功能衰竭等严重并发症。其适度的成本并不影响OA的成本效益,支持其在脊髓性肌萎缩症治疗中的变革性作用。
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来源期刊
Pharmacology Research & Perspectives
Pharmacology Research & Perspectives Pharmacology, Toxicology and Pharmaceutics-General Pharmacology, Toxicology and Pharmaceutics
CiteScore
5.30
自引率
3.80%
发文量
120
审稿时长
20 weeks
期刊介绍: PR&P is jointly published by the American Society for Pharmacology and Experimental Therapeutics (ASPET), the British Pharmacological Society (BPS), and Wiley. PR&P is a bi-monthly open access journal that publishes a range of article types, including: target validation (preclinical papers that show a hypothesis is incorrect or papers on drugs that have failed in early clinical development); drug discovery reviews (strategy, hypotheses, and data resulting in a successful therapeutic drug); frontiers in translational medicine (drug and target validation for an unmet therapeutic need); pharmacological hypotheses (reviews that are oriented to inform a novel hypothesis); and replication studies (work that refutes key findings [failed replication] and work that validates key findings). PR&P publishes papers submitted directly to the journal and those referred from the journals of ASPET and the BPS
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