Brigante Alejandro, Russo Barbara, Mongin Denis, Lauper Kim, Allali Danièle, Courvoisier Delphine S, Iudici Michele
Sanatorio Güemes, Ciudad Autónoma de Buenos Aires, Argentina.
University of Geneva, and Geneva University Hospitals, Geneva, Switzerland.
Arthritis Care Res (Hoboken). 2023 Apr;75(4):921-929. doi: 10.1002/acr.24854. Epub 2022 Nov 13.
To assess the proportion, the reasons, and the factors associated with the discontinuation or nonpublication of randomized controlled trials (RCTs) on connective tissue diseases (CTDs).
We searched all interventional RCTs on CTDs registered in ClinicalTrials.gov since 2000. Two reviewers selected studies according to prespecified eligibility criteria. Completion status, publication status, and reported reasons for discontinuation or nonpublication were retrieved on ClinicalTrials.gov, through literature search, and by contacting investigators. Multivariable logistic regression was used to identify factors associated with study noncompletion and nonpublication.
We included 175 studies, mostly phase III, placebo-controlled trials on pharmacologic treatments recruiting patients with systemic lupus erythematosus (51%), systemic sclerosis (20%), Sjögren's syndrome (12%), or other CTDs. Fifty-eight (33%) had been discontinued, mainly for insufficient patient accrual, with no differences in discontinuation rates across the CTDs (P > 0.5). Forty-six (35%) of 130 studies having included at least 1 patient were unpublished, and 86 (65%) were published in a peer-reviewed journal after a median of 24 months (interquartile range 15-41) from completion, with a significantly higher publication rate in completed versus discontinued studies (81% versus 22%; P < 0.001). We were able to obtain reasons for nonpublication in one-third of cases. Small sample size (<100 participants) was the only factor associated with study noncompletion and nonpublication.
One of 3 registered RCTs on CTDs fails to be completed or published. This represents a waste of resources and raises ethical concerns regarding hidden clinical data and unfruitful participation by patients.
评估结缔组织病(CTD)随机对照试验(RCT)终止或未发表的比例、原因及相关因素。
检索自2000年以来在ClinicalTrials.gov注册的所有关于CTD的干预性RCT。两名研究者根据预先设定的纳入标准选择研究。通过ClinicalTrials.gov、文献检索及联系研究者获取研究的完成状态、发表状态及报告的终止或未发表原因。采用多变量逻辑回归确定与研究未完成和未发表相关的因素。
我们纳入了175项研究,大多为III期、针对药物治疗的安慰剂对照试验,招募系统性红斑狼疮(51%)、系统性硬化症(20%)、干燥综合征(12%)或其他CTD患者。58项(33%)研究已终止,主要原因是患者入组不足,各CTD的终止率无差异(P>0.5)。在纳入至少1例患者的130项研究中,46项(35%)未发表,86项(65%)在完成后中位24个月(四分位间距15 - 41)在同行评审期刊上发表,完成的研究发表率显著高于终止的研究(81%对22%;P<0.001)。我们在三分之一的案例中能够获取未发表原因。小样本量(<100名参与者)是与研究未完成和未发表相关的唯一因素。
三分之一已注册的CTD-RCT未能完成或发表。这既浪费资源,也引发了对隐藏临床数据及患者无意义参与的伦理担忧。