Comparison between Reference Infliximab (Remicade) and its Biosimilar (Remsima) in Patients with Ankylosing Spondylitis: A Field-based Pharmacoeconomic Study

Hasan Raid Fadhil, A. A. Al-Jumaili, Nizar Abdulateef Al Ani
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Abstract

Background: Ankylosing spondylitis is a chronic inflammatory disease that mostly involves the spine and sacroiliac joints. It is associated with a decreased quality of life. Biological medicines such as infliximab and its biosimilar are the mainstay treatments for active ankylosing spondylitis. Objective: The study objective was to conduct a pharmacoeconomic study comparing the cost-effectiveness of the reference infliximab with its biosimilar in ankylosing spondylitis patients visiting public hospitals. Subjects and Method: This is a two-center pharmacoeconomic study performed at two large teaching governmental hospitals in Baghdad, Iraq, which supplied infliximab to outpatients with ankylosing spondylitis. The outcome data were obtained from patient’s medical records and face-to-face interviews with the patients from December 2021 through April 2022. The Independent T-Test was used to measure the differences in areas of utility, and quality of life, between the two infliximab groups. Results: The study recruited 62 patients with ankylosing spondylitis who received infliximab (31 received Remicade, and 31 received Remsima) for at least 12 weeks at two public teaching hospitals. The mean age of the patients was 37.85 years and 83.9% were men. In general, both reference infliximab and its biosimilar were successful in increasing the quality of life. Their importation costs were different from 2019 to 2021. The incremental cost-effectiveness ratio of reference infliximab versus biosimilar was $ 40,909/quality-adjusted life year (QALY) according to 2019 pricing. In contrast, in 2021 reference infliximab (Remicade) was less expensive and yielded slightly better quality of life improvement than biosimilar (Remsima) making Remicade more cost-effective (dominant). Conclusion: Remicade was slightly superior to Remsima in quality of life improvement. However, it was difficult to determine whether the reference or its biosimilar was more cost-effective in 2019 because the health officials did not specify a willingness to pay per quality-adjusted life year. Compared to Remsima, Remicade was more cost-effective in 2021 because it was less expensive and more effective in terms of quality of life improvement.
对照英夫利昔单抗(Remicade)及其生物类似物(Remsima)在强直性脊柱炎患者中的比较:一项基于现场的药物经济学研究
背景:强直性脊柱炎是一种主要累及脊柱和骶髂关节的慢性炎症性疾病。它与生活质量下降有关。英夫利昔单抗及其生物类似物等生物药物是治疗活动性强直性脊柱炎的主要药物。目的:本研究的目的是进行一项药物经济学研究,比较在公立医院就诊的强直性脊柱炎患者中参考英夫利昔单抗与其生物类似物的成本效益。受试者和方法:这是一项在伊拉克巴格达的两家大型政府教学医院进行的双中心药物经济学研究,该医院为强直性脊柱炎门诊患者提供英夫利昔单抗。结果数据来自患者的医疗记录和2021年12月至2022年4月对患者的面对面访谈。独立T检验用于测量两组英夫利昔单抗在效用和生活质量方面的差异。结果:该研究招募了62名强直性脊柱炎患者,他们在两家公立教学医院接受了英夫利昔单抗治疗(31名接受了Remicade治疗,31名接受Remsima治疗)至少12周。患者的平均年龄为37.85岁,83.9%为男性。总的来说,参考英夫利昔单抗及其生物类似物都成功地提高了生活质量。从2019年到2021年,它们的进口成本有所不同。根据2019年的定价,参考英夫利昔单抗与生物仿制药的增量成本效益比为40909/质量调整生命年(QALY)。相比之下,2021年的参考英夫利昔单抗(Remicade)比生物仿制药(Remsima)便宜,生活质量改善效果略好,使Remicade更具成本效益(优势)。结论:Remicade在生活质量改善方面略优于Remsima。然而,由于卫生官员没有具体说明是否愿意为每个质量调整后的生命年支付费用,因此很难确定2019年参考品或其生物仿制品是否更具成本效益。与Remsima相比,Remicade在2021年更具成本效益,因为它在改善生活质量方面更便宜、更有效。
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
0.10
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0.00%
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34
审稿时长
12 weeks
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