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首页> 外文期刊>BioMed research international >Predictive Factors of Clinical Response of Infliximab Therapy in Active Nonradiographic Axial Spondyloarthritis Patients
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Predictive Factors of Clinical Response of Infliximab Therapy in Active Nonradiographic Axial Spondyloarthritis Patients

机译:主动非放射照相型轴突性脊柱关节炎患者英夫利昔单抗治疗临床反应的预测因素

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Objectives.To evaluate the efficiency and the predictive factors of clinical response of infliximab in active nonradiographic axial spondyloarthritis patients.Methods.Active nonradiographic patients fulfilling ESSG criteria for SpA but not fulfilling modified New York criteria were included. All patients received infliximab treatment for 24 weeks. The primary endpoint was ASAS20 response at weeks 12 and 24. The abilities of baseline parameters and response at week 2 to predict ASAS20 response at weeks 12 and 24 were assessed using ROC curve and logistic regression analysis, respectively.Results.Of 70 axial SpA patients included, the proportions of patients achieving an ASAS20 response at weeks 2, 6, 12, and 24 were 85.7%, 88.6%, 87.1%, and 84.3%, respectively. Baseline MRI sacroiliitis score (AUC = 0.791;P=0.005), CRP (AUC = 0.75;P=0.017), and ASDAS (AUC = 0.778,P=0.007) significantly predicted ASAS20 response at week 12. However, only ASDAS (AUC = 0.696,P=0.040) significantly predicted ASAS20 response at week 24. Achievement of ASAS20 response after the first infliximab infusion was a significant predictor of subsequent ASAS20 response at weeks 12 and 24 (waldχ2=6.87,P=0.009, and waldχ2=5.171,P=0.023).Conclusions.Infliximab shows efficiency in active nonradiographic axial spondyloarthritis patients. ASDAS score and first-dose response could help predicting clinical efficacy of infliximab therapy in these patients.
机译:目的:评价英夫利昔单抗在活动性非放射线轴性脊椎关节炎患者中的疗效和预测因素。方法:包括在活动中非放射线患者符合SpA的ESSG标准,但不满足纽约州标准的修改。所有患者接受英夫利昔单抗治疗24周。主要终点是第12和24周的ASAS20应答。分别使用ROC曲线和Logistic回归分析评估基线参数和第2周的应答预测第12和24周的ASAS20应答的能力。结果:70例轴向SpA患者包括在内,在第2、6、12和24周达到ASAS20反应的患者比例分别为85.7%,88.6%,87.1%和84.3%。基线MRI cro关节炎评分(AUC = 0.791; P = 0.005),CRP(AUC = 0.75; P = 0.017)和ASDAS(AUC = 0.778,P = 0.007)显着预测了第12周的ASAS20反应。但是,只有ASDAS(AUC = 0.696,P = 0.040)在第24周时显着预测了ASAS20反应。首次英夫利昔单抗输注后获得ASAS20反应是在第12和24周时随后ASAS20反应的重要预测指标(waldχ2= 6.87,P = 0.009,以及waldχ2= 5.171)。 ,P = 0.023)。结论。英夫利昔单抗显示出对非放射性活动性轴索性脊柱关节炎患者有效。 ASDAS评分和首剂反应可以帮助预测英夫利昔单抗在这些患者中的临床疗效。

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