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生物制剂注册在非洲和中东的实际价值:挑战与机遇。

The practical value of biologics registries in Africa and Middle East: challenges and opportunities.

机构信息

University Mohammed Vth Souissi, Rabat, Morocco.

出版信息

Clin Rheumatol. 2012 Mar;31(3):407-16. doi: 10.1007/s10067-011-1918-8. Epub 2012 Jan 7.

Abstract

Biologics, including tumor necrosis factor (TNF) inhibitors, are increasingly used for the treatment of inflammatory conditions such as rheumatoid arthritis (RA), psoriatic arthritis, and ankylosing spondylitis. The efficacy of these drugs has been demonstrated in randomized controlled trials (RCTs). However, these studies are conducted in controlled environments, and the results may not necessarily reflect clinical outcomes in daily clinical practice. In Europe and other western countries, numerous biologics registries that enroll and monitor patients receiving biologics have been established. These registries follow patients irrespective of whether they continue with the initial biologic drug. Thus, real-life efficacy data from these registries can be used to assess the long-term safety of biologics through longitudinal studies. In Africa and Middle East (AFME), such registries currently exist only in Morocco and South Africa. In light of the increasing availability of biologics and scarcity of long-term safety data of these agents in the AFME population, there is a need to establish biologics registries in other countries across the region. This review discusses the value of biologics registries versus RCTs as well as safety and efficacy data from observational studies presented as lessons from well-established biologics registries. In addition, the rationale for establishing such registries in the AFME region is also presented.

摘要

生物制剂,包括肿瘤坏死因子(TNF)抑制剂,越来越多地用于治疗炎症性疾病,如类风湿关节炎(RA)、银屑病关节炎和强直性脊柱炎。这些药物的疗效已在随机对照试验(RCT)中得到证实。然而,这些研究是在受控环境中进行的,结果不一定反映日常临床实践中的临床结果。在欧洲和其他西方国家,已经建立了许多登记和监测接受生物制剂治疗的患者的生物制剂登记处。这些登记处无论患者是否继续使用最初的生物药物,都会对其进行跟踪。因此,这些登记处的真实疗效数据可通过纵向研究用于评估生物制剂的长期安全性。在非洲和中东(AFME),此类登记处目前仅在摩洛哥和南非存在。鉴于生物制剂的可获得性不断增加,以及这些药物在 AFME 人群中的长期安全性数据稀缺,需要在该地区的其他国家建立生物制剂登记处。这篇综述讨论了生物制剂登记处与 RCT 相比的价值,以及作为从成熟的生物制剂登记处获得的经验教训提出的观察性研究中的安全性和疗效数据。此外,还提出了在 AFME 地区建立此类登记处的基本原理。

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