首页> 外文期刊>Arthritis research & therapy. >Association of serum markers with improvement in clinical response measures after treatment with golimumab in patients with active rheumatoid arthritis despite receiving methotrexate: results from the GO-FORWARD study.
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Association of serum markers with improvement in clinical response measures after treatment with golimumab in patients with active rheumatoid arthritis despite receiving methotrexate: results from the GO-FORWARD study.

机译:尽管接受甲氨蝶呤治疗的活动性类风湿关节炎患者在接受戈利木单抗治疗后血清标志物与临床反应措施改善之间的关联:GO-FORWARD研究的结果。

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INTRODUCTION: The goal of this study was to identify serum markers that are modulated by treatment with golimumab with or without methotrexate (MTX) and are associated with clinical response. METHODS: Sera were collected at weeks 0 and 4 from a total of 336 patients (training dataset, n = 100; test dataset, n = 236) from the GO-FORWARD study of patients with active rheumatoid arthritis despite MTX. Patients were randomly assigned to receive placebo plus MTX; golimumab, 100 mg plus placebo; golimumab, 50 mg plus MTX; or golimumab, 100 mg plus MTX. Subcutaneous injections were administered every 4 weeks. Samples were tested for select inflammatory, bone, and cartilage markers and for protein profiling using multianalyte profiles. RESULTS: Treatment with golimumab with or without MTX resulted in significant decreases in a variety of serum proteins at week 4 as compared with placebo plus MTX. The American College of Rheumatology (ACR) 20, ACR 50, and Disease Activity Score (DAS) 28 responders showed a distinct biomarker profile compared with nonresponding patients. CONCLUSIONS: ACR 20 and ACR 50 responders among the golimumab/golimumab + MTX-treated patients had a distinct change from baseline to week 4 in serum protein profile as compared with nonresponders. Some of these changed markers were also associated with multiple clinical response measures and improvement in outcome measures in golimumab/golimumab + MTX-treated patients. Although the positive and negative predictive values of the panel of markers were modest, they were stronger than C-reactive protein alone in predicting clinical response to golimumab. TRIAL REGISTRATION: http://ClinicalTrials.gov identification number: NCT00264550.
机译:简介:本研究的目的是鉴定血清标记物,该标记物可通过接受或不接受甲氨蝶呤(MTX)的戈利木单抗治疗而调节,并与临床反应相关。方法:在第0和第4周,从接受MTX治疗的活动性类风湿关节炎患者的GO-FORWARD研究中,总共从336例患者中收集了血清(训练数据集,n = 100;测试数据集,n = 236)。患者被随机分配接受安慰剂加MTX治疗;戈利木单抗100毫克加安慰剂;戈利木单抗,50 mg加MTX;或戈利木单抗100毫克加MTX。每4周皮下注射一次。使用多分析物谱对样品进行了选择的炎性,骨和软骨标志物测试以及蛋白质谱分析。结果:与安慰剂加MTX相比,在有或没有MTX的情况下用戈利木单抗治疗导致第4周各种血清蛋白的显着降低。与无反应的患者相比,美国风湿病学会(ACR)20,ACR 50和疾病活动评分(DAS)28的反应者表现出明显的生物标志物特征。结论:经戈利木单抗/戈利木单抗+ MTX治疗的患者中,ACR 20和ACR 50应答者与无应答者相比,从基线到第4周血清蛋白谱有明显变化。这些改变的标志物中的一些还与戈利木单抗/戈利木单抗+ MTX治疗的患者的多种临床反应措施和预后措施的改善有关。尽管这组标志物的阳性和阴性预测值均中等,但在预测对戈利木单抗的临床反应时,它们比单独的C反应蛋白强。试用注册:http://ClinicalTrials.gov标识号:NCT00264550。

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