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Dose escalation of infliximab in clinical practice: improvements seen may be explained by a regression-like effect

机译:英夫利昔单抗的剂量递增在临床实践中:所见的改善可能由类似回归的效应解释

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摘要

>Objective: To determine whether increased infliximab doses result in better clinical outcome in rheumatic diseases. >Methods: Subjects were 124 patients with rheumatoid arthritis treated with biological agents at a single institute. Index cases were 44 patients whose infliximab doses had been increased. Controls were patients treated with infliximab without dose increase (n = 44), and patients treated with etanercept (n = 36). Disease activity score (DAS28), ACR28 swollen joint counts, and numerical ACR responses were compared before and after dose increases. For the controls, the point at which the DAS28 value showed any increase (despite infliximab/etanercept treatment) was used as the reference time point. Comparisons were made between three sets of outcomes: best outcome achieved before the dose increase (cases) or before the reference time point (controls); outcomes at this point; and best outcomes after this point. >Results: Following dose increase, disease activity showed modest but statistically significant improvements. The improvement achieved after dosage escalation was equal to, but not better than, the best values before dose escalation. While this finding could be interpreted as "recapturing" the previous response, similar improvements were seen in both control groups. Thus the same pattern of worsening and subsequent improvement was seen with or without the infliximab dose increase. >Conclusions: Clinical improvement with increased infliximab dose, and the impression that a previous response can be "recaptured" with higher doses, cannot be taken at face value, as similar improvements occurred in two control groups. The use of infliximab at doses higher than 3 mg/kg needs to be evaluated further.
机译:>目的:要确定英夫利昔单抗剂量的增加是否能在风湿性疾病中带来更好的临床效果。 >方法:对象是在一家机构中用生物制剂治疗的124名类风湿关节炎患者。索引病例为44例英夫利昔单抗剂量增加的患者。对照组为未增加剂量的英夫利昔单抗治疗的患者(n = 44)和依那西普治疗的患者(n = 36)。在增加剂量之前和之后比较疾病活动评分(DAS28),ACR28肿胀关节计数和数字ACR反应。对于对照,将DAS28值显示出任何增加的点(尽管英夫利昔单抗/依那西普治疗)用作参考时间点。在三组结果之间进行了比较:剂量增加之前(病例)或参考时间点之前的最佳结果(对照组);此时的结果;在此之后取得最佳结果。 >结果:剂量增加后,疾病活动显示出适度但有统计学意义的改善。剂量增加后获得的改善与剂量增加前的最佳值相等,但并不比其更好。尽管这一发现可以解释为“重新捕获”了先前的反应,但在两个对照组中都看到了类似的改善。因此,无论有无英夫利昔单抗剂量增加,都观察到恶化和随后改善的相同模式。 >结论:英夫利昔单抗剂量的增加可改善临床症状,以前的反应可以用更高的剂量“重获”的印象不能从表面上体现出来,因为两个对照组发生了类似的改善。英夫利昔单抗以高于3 mg / kg的剂量使用需要进一步评估。

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