稳定期患者因非医学原因从一种参考生物制剂转用另一种参考生物制剂:文献检索和简要综述。

Q2 Medicine
Journal of market access & health policy Pub Date : 2021-08-20 eCollection Date: 2021-01-01 DOI:10.1080/20016689.2021.1964792
Knut Stavem
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引用次数: 0

摘要

背景:从参考生物药(原研药)到生物仿制药的非医疗转换(NMS)做法在一些国家已被广泛接受。然而,有关从一种原研药到另一种原研药的非医疗转换(NMS)的影响的文献却很少。目标:根据现有文献,评估从一种生物原研药到另一种生物原研药的 NMS 对患者的影响。重点关注三个疾病领域中 TNF-α 抑制剂的疗效和治疗成本。研究方法在Ovid(PubMed、EMBASE)和主要治疗领域会议的摘要中进行文献检索,以确定报告在原研生物制剂之间转换疗效、安全性或成本的研究。结果:确定了 167 篇参考文献并筛选了摘要;对 36 篇论文进行了全文审阅,其中 6 篇符合纳入标准。三项关于 NMS 的临床研究样本量很小,但表明 NMS 是有益的。其余三项研究使用的是行政数据,几乎没有临床信息,这表明 NMS 是不利的,会增加医疗使用率和成本。结论:关于 NMS 的文献资料非常有限,从一种原产生物到另一种原产生物,文献资料存在方法上的局限性。研究结果喜忧参半,无法得出压倒性结论。未来的研究是有必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Switching from one reference biological to another in stable patients for non-medical reasons: a literature search and brief review.

Switching from one reference biological to another in stable patients for non-medical reasons: a literature search and brief review.

Switching from one reference biological to another in stable patients for non-medical reasons: a literature search and brief review.

Background: The practice of non-medical switch (NMS) from a reference biological (originator) to a biosimilar is widely accepted in some countries. However, there is little documentation on the impact of NMS from one originator to another originator. Objectives: To assess the consequences for patients of NMS from one biological originator to another, based on existing literature. The focus was on efficacy and cost of treatment with TNF-α-inhibitors in three disease areas. Methods: A literature search was conducted in Ovid (PubMed, EMBASE) and abstracts from meetings in key therapeutic areas, to identify studies reporting efficacy, safety or costs by switching between originator biologics. Results: 167 references were identified and abstracts screened; 36 papers reviewed in full text, and 6 fulfilled the inclusion criteria. Three clinical studies of NMS had very small sample sizes, but suggested that NMS is beneficial. The remaining three studies used administrative data with little clinical information, indicating that NMS was disadvantageous and associated with increased health care utilization and costs. Conclusions: There is very limited documentation on NMS from one originator biological to another, and the literature suffers from methodological limitations. The results are mixed and preclude drawing an overriding conclusion. Future studies, are warranted.

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