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首页> 外文期刊>Clinical and experimental rheumatology >Inclusion criteria as widely used for rheumatoid arthritis clinical trials: patient eligibility in a Turkish cohort.
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Inclusion criteria as widely used for rheumatoid arthritis clinical trials: patient eligibility in a Turkish cohort.

机译:类风湿关节炎临床试验中广泛使用的纳入标准:土耳其队列中的患者资格。

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摘要

OBJECTIVE: To identify the proportion of patients fulfilling the inclusion criteria widely used in most clinical trials for rheumatoid arthritis (RA)--including the recent clinical trials of anti-Tumor Necrosis Factor alpha (TNFalpha) agents--in a Turkish cohort. METHODS: 186 consecutive RA patients attending a routine tertiary rheumatology clinic were evaluated in 2 groups: Early RA group (group E): 31 patients with a disease duration of < or = 3 years (mean: 1.9 +/- 0.9 years); late RA group (group L): 155 patients with a disease duration of > 3 years (mean: 13.3 +/- 8.6 years). Patients were evaluated according to 2 different sets of inclusion criteria: (i) The widely used common inclusion criteria for RA clinical studies, as outlined by Sokka and Pincus; (ii) the criteria of two major anti-TNF clinical studies, ERA and ATTRACT. RESULTS: No patients in group E, and 9 (6%) patients in group L fulfilled the common criteria used in clinical studies for RA. In group E, 28 patients had already been started on methotrexate; 2 patients were on sulphasalazine and one patient was on leflunomide. Nevertheless, even if the criterion for previous use of methotrexate was not applied patients did not fulfill the rest of the criteria of ERA study. In group L, 9 out of 155 patients (6%) met the criteria for the ATTRACT study. CONCLUSION: Only few patients met the widely used inclusion criteria for most RA clinical trials and the recent clinical trials of TNFalpha agents in this Turkish cohort. This may be explained by the milder disease activity in this geographical region, which further emphasizes the need to consider development of new criteria for inclusion in clinical trials.
机译:目的:确定在土耳其队列中符合风湿性关节炎(RA)的大多数临床试验(包括最近抗肿瘤坏死因子α(TNFalpha)药物的最新临床试验)广泛使用的纳入标准的患者比例。方法:将186例连续三级风湿病门诊就诊的RA患者分为两组:早期RA组(E组):31例病程<或= 3年(平均:1.9 +/- 0.9岁);晚期RA组(L组):155名患者,病程> 3年(平均:13.3 +/- 8.6年)。根据2套不同的纳入标准对患者进行评估:(i)如Sokka和Pincus概述的,广泛用于RA临床研究的通用纳入标准; (ii)两项主要抗TNF临床研究的标准,即ERA和ATTRACT。结果:E组中没有患者,L组中有9(6%)患者符合用于RA临床研究的通用标准。在E组中,已有28例患者开始接受甲氨蝶呤治疗; 2例患者使用柳氮磺胺吡啶,1例患者使用来氟米特。但是,即使不使用以前使用甲氨蝶呤的标准,患者也不能满足ERA研究的其他标准。在L组中,155名患者中有9名(6%)达到了ATTRACT研究的标准。结论:在该土耳其人群中,只有少数患者符合大多数RA临床试验和TNFα药物近期临床试验的广泛纳入标准。这可能是因为该地理区域的疾病活动较为温和,这进一步强调了需要考虑制定新的纳入临床试验标准的必要性。

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