Focus on biosimilar etanercept - bioequivalence and interchangeability.

IF 5.3 Q1 MEDICINE, RESEARCH & EXPERIMENTAL Biologics : Targets & Therapy Pub Date : 2018-08-30 eCollection Date: 2018-01-01 DOI:10.2147/BTT.S126854
Fabrizio Cantini, Maurizio Benucci
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引用次数: 0

Abstract

Background: The recent approval of reference etanercept (re-ETN) biosimilars SB4, GP2015, and HD203 produced relevant changes in the management of rheumatoid arthritis (RA), psoriatic arthritis, and ankylosing spondylitis due to the considerably lower cost of these products and the consequent savings.

Aims: To review the pharmacodynamics, pharmacokinetics, efficacy, and safety of ETN biosimilars when employed as first-line therapy or after transition from re-ETN. Patients' acceptability was also addressed.

Evidence review: The available literature was reviewed through a search of PubMed database, and abstract books of the American College for Rheumatology and European League Against Rheumatism annual meetings. SB4, GP2015, and HD203 were licensed by the US, European and South Korea regulatory agencies after the bioequivalence to re-ETN was demonstrated through pharmacodynamic and pharmacokinetic studies, and randomized, head to head, controlled trials. Based on the evidence of efficacy and safety of SB4 and HD203 in RA, and of GP2015 in psoriasis, by the extrapolation principle, the three biosimilars were approved for all indications licensed for re-ETN, and the regulatory agencies introduced the interchangeability from the originator to the biosimilar. Extrapolation of indications, and particularly interchangeability raised relevant concerns among the rheumatologists due to the low level of evidence supporting the switching strategy (or transition). Rheumatologists' concerns are oriented toward the relevant number of biosimilar discontinuations after the transition ranging from 7%-17% over a short-term follow-up period. As resulted from two studies, at least 20%-30% of the patients claimed more exhaustive information on the switching procedure.

Conclusion: Based on the available evidence, re-ETN biosimilars may be a good option as first-line therapy, while further data are needed to definitively establish the efficacy, safety, and the economic reflexes of transitioning from re-ETN.

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重点关注生物仿制药依那西普的生物等效性和互换性。
背景:最近批准的参考依那西普(re-ETN)生物仿制药SB4、GP2015和HD203在类风湿性关节炎(RA)、银屑病关节炎和强直性脊柱炎的治疗中产生了相关变化,因为这些产品的成本显著降低,并因此节省了费用。目的:综述ETN生物仿制药在用作一线治疗或从再ETN过渡后的药效学、药代动力学、疗效和安全性。患者的可接受性也得到了解决。证据综述:通过检索PubMed数据库以及美国风湿病学会和欧洲抗风湿病联盟年会的摘要书籍,对现有文献进行了综述。SB4、GP2015和HD203获得了美国、欧洲和韩国监管机构的许可,此前通过药效学和药代动力学研究以及随机、头对头对照试验证明了re-ETN的生物等效性。根据SB4和HD203治疗RA和GP2015治疗银屑病的有效性和安全性证据,根据外推原则,这三种生物仿制药被批准用于所有许可用于再ETN的适应症,监管机构引入了从原始生物到生物仿制药的互换性。适应症的推断,特别是互换性,由于支持转换策略(或过渡)的证据水平较低,引起了风湿病学家的相关担忧。风湿病学家关注的是,在短期随访期间,过渡后生物类似物的停用数量在7%-17%之间。根据两项研究的结果,至少20%-30%的患者声称对转换程序有更详尽的信息。结论:根据现有证据,再ETN生物仿制药可能是一线治疗的良好选择,同时还需要进一步的数据来确定从再ETN过渡的疗效、安全性和经济反应。
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来源期刊
Biologics : Targets & Therapy
Biologics : Targets & Therapy MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
8.30
自引率
0.00%
发文量
22
审稿时长
16 weeks
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