Walker Ulrich A, Clements Philip J, Allanore Yannick, Distler Oliver, Oddis Chester V, Khanna Dinesh, Furst Daniel E
Department of Rheumatology, Basel University, Basel, Switzerland.
Department of Rheumatology, David Geffen School of Medicine at University of California Los Angeles, Los Angeles, CA, USA.
Rheumatology (Oxford). 2017 Sep 1;56(suppl_5):v38-v44. doi: 10.1093/rheumatology/kex196.
SSc is clinically and pathogenetically heterogeneous. Consensus standards for trial design and outcome measures are needed. International experts experienced in SSc clinical trial design and a researcher experienced in systematic literature review screened the PubMed and Cochrane Central Register of Controlled Trials in order to develop points to consider when planning a clinical trial for muscle involvement in SSc. The experts conclude that SSc-associated muscle involvement is heterogeneous and lacks a universally accepted gold-standard for measuring therapeutic response. Although outcome studies are currently limited by the inability to clearly distinguish active, reversible muscle inflammation from irreversible muscle damage and extramuscular organ involvement, strong consideration should be given to enrolling patients with a myopathy that features several elements of likely reversibility such as muscle weakness, biopsy-proven active inflammation, an MRI indicating muscle inflammation and a baseline serum creatinine kinase above three times the upper limit of normal to prevent floor effect. Randomized controlled trials are preferred, with a duration of at least 24 weeks. Outcome measures should include a combination of elements that are likely to be reversible, such as muscle weakness, biopsy-proven active inflammation, creatinine kinase/aldolase and a quality of life questionnaire. The individual measurements might require a short pre-study for further validation. A biological sample repository is recommended.
系统性硬化症在临床和发病机制上具有异质性。需要制定试验设计和结果测量的共识标准。在系统性硬化症临床试验设计方面经验丰富的国际专家以及在系统文献综述方面经验丰富的研究人员对PubMed和Cochrane对照试验中央注册库进行了筛选,以便制定在规划系统性硬化症肌肉受累的临床试验时需要考虑的要点。专家们得出结论,系统性硬化症相关的肌肉受累具有异质性,并且缺乏用于衡量治疗反应的普遍接受的金标准。尽管目前的结果研究受到无法清晰区分活动性、可逆性肌肉炎症与不可逆性肌肉损伤及肌肉外器官受累的限制,但应强烈考虑纳入患有肌病的患者,这些患者具有一些可能可逆的特征,如肌肉无力、活检证实的活动性炎症、显示肌肉炎症的MRI以及基线血清肌酸激酶高于正常上限的三倍,以防止出现地板效应。首选随机对照试验,持续时间至少为24周。结果测量应包括可能可逆的因素的组合,如肌肉无力、活检证实的活动性炎症、肌酸激酶/醛缩酶以及生活质量问卷。个别测量可能需要在研究前进行简短的进一步验证。建议建立生物样本库。