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The TRACTISS protocol: a randomised double blind placebo controlled clinical trial of anti-B-cell therapy in patients with primary Sjögren's Syndrome.

机译:TRaCTIss方案:一项随机双盲安慰剂对照临床试验,用于治疗原发性干燥综合征患者的抗B细胞治疗。

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摘要

Background: Primary Sjögren's Syndrome (PSS) mainly affects women (9:1 female:male ratio) and is one of the commonest autoimmune diseases with a prevalence of 0.1 - 0.6% of adult women. For patients with PSS there is currently no effective therapy that can alter the progression of the disease. The aim of the TRACTISS study is to establish whether in patients with PSS, treatment with rituximab improves clinical outcomes. Methods/design: TRACTISS is a UK multi-centre, double-blind, randomised, controlled, parallel group trial of 110 patients with PSS. Patients will be randomised on a 1:1 basis to receive two courses of either rituximab or placebo infusion in addition to standard therapy, and will be followed up for up to 48 weeks. The primary objective is to assess the extent to which rituximab improves symptoms of fatigue and oral dryness. Secondary outcomes include ocular dryness, salivary flow rates, lacrimal flow, patient quality of life, measures of disease damage and disease activity, serological and peripheral blood biomarkers, and glandular histology and composition. Discussion: The TRACTISS trial will provide direct evidence as to whether rituximab in patients with PSS leads to an improvement in patient symptoms and a reduction in disease damage and activity. Trial registration: UKCRN Portfolio ID: 9809 ISRCTN65360827.
机译:背景:原发性干燥综合征(PSS)主要影响女性(女性与男性的比例为9:1),是最常见的自身免疫性疾病之一,患病率为成年女性的0.1-0.6%。对于PSS患者,目前尚没有可以改变疾病进展的有效疗法。 TRACTISS研究的目的是确定在PSS患者中,利妥昔单抗治疗是否可以改善临床结局。方法/设计:TRACTISS是英国的一项多中心,双盲,随机,对照,平行分组研究,涉及110名PSS患者。除标准治疗外,患者将按1:1的比例随机接受两个疗程的利妥昔单抗或安慰剂输注,并将接受长达48周的随访。主要目的是评估利妥昔单抗改善疲劳和口腔干燥症状的程度。次要结果包括眼干燥,唾液流速,泪流,患者生活质量,疾病损害和疾病活动的测量,血清学和外周血生物标志物以及腺组织学和成分。讨论:TRACTISS试验将直接提供利妥昔单抗治疗PSS患者是否可改善患者症状,减少疾病损害和活动的证据。试用注册:UKCRN产品组合ID:9809 ISRCTN65360827。

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