Hospital for Special Surgery, Weill Medical College of Cornell University, New York, NY, USA.
Lupus. 2011 Feb;20(2):219-24. doi: 10.1177/0961203310395053.
The Antiphospholipid Syndrome (APS) Clinical Research Task Force (CRTF) was one of six Task Forces developed by the 13(th) International Congress on Antiphospholipid Antibodies (aPL) organization committee with the purpose of: a) evaluating the limitations of APS clinical research and developing guidelines for researchers to help improve the quality of APS research; and b) prioritizing the ideas for a well-designed multicenter clinical trial and discussing the pragmatics of getting such a trial done. Following a systematic working algorithm, the Task Force identified five major issues that impede APS clinical research and the ability to develop evidence-based recommendations for the management of aPL-positive patients: (1) aPL detection has been based on partially or non-standardized tests, and clinical (and basic) APS research studies have included patients with heterogeneous aPL profiles with different clinical event risks; (2) clinical (and basic) APS research studies have included a heterogeneous group of patients with different aPL-related manifestations (some controversial); (3) thrombosis and/or pregnancy risk stratification and quantification are rarely incorporated in APS clinical research; (4) most APS clinical studies include patients with single positive aPL results and/or low-titer aPL ELISA results; furthermore, study designs are mostly retrospective and not population based, with limited number of prospective and/or controlled population studies; and (5) lack of the understanding the particular mechanisms of aPL-mediated clinical events limits the optimal clinical study design. The Task Force recommended that there is an urgent need for a truly international collaborative approach to design and conduct well-designed prospective large-scale multi-center clinical trials of patients with persistent and clinically significant aPL profiles. An international collaborative meeting to formulate a good research question using 'FINER' (Feasible; Interesting; Novel; Ethical; and Relevant) criteria took place in November 2010.
抗磷脂综合征(APS)临床研究工作组(CRTF)是由第 13 届国际抗磷脂抗体(aPL)大会组织委员会成立的六个工作组之一,其目的是:a)评估 APS 临床研究的局限性,并为研究人员制定指导方针,以帮助提高 APS 研究的质量;b)为精心设计的多中心临床试验确定优先事项,并讨论开展此类试验的实际问题。该工作组遵循系统的工作算法,确定了五个主要问题,这些问题阻碍了 APS 临床研究的开展,并影响了为 aPL 阳性患者制定基于证据的管理建议:(1)aPL 的检测基于部分或非标准化的检测方法,而临床(和基础)APS 研究纳入了具有不同临床事件风险的具有不同 aPL 谱的异质性患者;(2)临床(和基础)APS 研究纳入了一组具有不同与 aPL 相关表现(一些有争议)的异质性患者;(3)血栓形成和/或妊娠风险分层和量化很少纳入 APS 临床研究;(4)大多数 APS 临床研究纳入了单个 aPL 阳性结果和/或低滴度 aPL ELISA 结果的患者;此外,研究设计大多是回顾性的,而不是基于人群的,前瞻性和/或对照人群研究的数量有限;(5)缺乏对 aPL 介导的临床事件特定机制的了解,限制了最佳临床研究设计。工作组建议,迫切需要采用真正的国际合作方法来设计和开展具有持久和临床显著 aPL 谱的患者的精心设计的前瞻性大规模多中心临床试验。2010 年 11 月,举行了一次国际合作会议,根据“可行性;有趣;新颖;伦理;相关”(FINER)标准制定了一个好的研究问题。