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巴瑞替尼治疗中重度类风湿关节炎的经济评价建模框架。

A modeling framework for the economic evaluation of baricitinib in moderate-to-severe rheumatoid arthritis.

机构信息

Real World Solutions, IQVIA, London, UK.

Global Patient Reported Outcomes and Real World Evidence (GPORWE) International, Eli Lilly, West Ryde, Australia.

出版信息

Expert Rev Pharmacoecon Outcomes Res. 2020 Apr;20(2):221-228. doi: 10.1080/14737167.2020.1744435. Epub 2020 Mar 25.

DOI:10.1080/14737167.2020.1744435
PMID:32212867
Abstract

: The approval in more than 50 countries of baricitinib, an oral Janus Kinase inhibitor for the treatment of Rheumatoid Arthritis (RA), warrants a framework for corresponding economic evaluations. To develop a comprehensive economic model assessing the cost-effectiveness of baricitinib for the treatment of moderately-to-severely active RA patients in comparison to other relevant treatments, considering the natural history of the disease, real world treatment patterns, and clinical evidence from the baricitinib trials.: A systematic literature review of previously developed models in RA was conducted to inform the model structure, key modeling assumptions and data inputs. Consultations with rheumatologists were undertaken to validate the modeling approach and underlying assumptions.: A discrete event simulation model was developed to international best practices with flexibility to assess the cost-effectiveness of baricitinib over a lifetime in a variety of markets. The model incorporates treatment sequencing to adequately reflect treatment pathways in clinical practice. Outcomes assessed include cost and quality-adjusted life years, allowing for a full incremental analysis of cost-effectiveness of competing treatments and treatment sequences.: The economic model developed provides a robust framework for future analyses assessing the cost-effectiveness of baricitinib for the treatment of RA in specific country settings.

摘要

在 50 多个国家批准巴利昔替尼用于治疗类风湿关节炎(RA),这为相应的经济评估提供了一个框架。为了开发一个全面的经济模型,评估巴利昔替尼治疗中度至重度活跃 RA 患者与其他相关治疗相比的成本效益,考虑到疾病的自然史、实际治疗模式和巴利昔替尼试验的临床证据:对 RA 中以前开发的模型进行了系统的文献回顾,以告知模型结构、关键建模假设和数据输入。与风湿病专家进行了磋商,以验证建模方法和基本假设。开发了一个离散事件模拟模型,以符合国际最佳实践,具有评估各种市场中巴利昔替尼终身成本效益的灵活性。该模型纳入了治疗顺序,以充分反映临床实践中的治疗途径。评估的结果包括成本和质量调整生命年,允许对竞争治疗和治疗顺序的成本效益进行全面的增量分析。所开发的经济模型为未来在特定国家环境中评估巴利昔替尼治疗 RA 的成本效益提供了一个强大的框架。

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引用本文的文献

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Clin Pharmacol Drug Dev. 2020 Nov;9(8):952-960. doi: 10.1002/cpdd.868. Epub 2020 Sep 17.