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英夫利昔单抗剂量与临床状况:针对1642例类风湿关节炎患者的两项研究结果

Infliximab dose and clinical status: results of 2 studies in 1642 patients with rheumatoid arthritis.

作者信息

Stern Richard, Wolfe Frederick

机构信息

University of Texas Southwestern Medical Center at Dallas, Dallas, Texas, USA.

出版信息

J Rheumatol. 2004 Aug;31(8):1538-45.

Abstract

OBJECTIVE

Infliximab is an effective anti-tumor necrosis factor (TNF) agent widely used in the treatment of rheumatoid arthritis (RA). Initially recommended at a dose of 3 mg/kg, subsequent label revisions allowed doses up to 10 mg/kg or at 4-week intervals rather than the originally suggested 8-week intervals, if clinically indicated. The doses used have implications for efficacy and costs, but no data exist for actual dose used in the US. This study evaluates the dosage and rates of increase in infliximab-treated patients with RA.

METHODS

Study 1: Review of patient charts and infusion records for 394 RA patients from 2 large rheumatology practices comprising 15 rheumatologists in Dallas, Texas. Study 2: Survey of 1324 RA patients using infliximab participating in a longitudinal study of RA outcomes. Patients completed a detailed questionnaire about clinical status and infliximab use.

RESULTS

The results of the 2 studies were similar: the average infliximab dose was 5 mg/kg, increasing most rapidly until the end of the first years, after which the increase was slowed. Increases > 3 mg/kg occurred in 61% of patients in Study 1 and 56% in Study 2. The 8-week treatment interval was almost universally used, and more than 95% of infusions occurred in this interval. The most common reason for increase in dose was insufficient response. Among patients who completed 4 infusions, 75% remained on therapy at 2 years after infliximab start. The average improvement in Health Assessment Questionnaire disability score was 0.28.

CONCLUSION

Infliximab dose increases are common, particularly during the first year of treatment. The average dose is 5 mg/kg. Seventy-five percent of patients continue using infliximab 2 years after treatment onset.

摘要

目的

英夫利昔单抗是一种有效的抗肿瘤坏死因子(TNF)药物,广泛用于治疗类风湿关节炎(RA)。最初推荐剂量为3mg/kg,随后标签修订允许剂量高达10mg/kg,或在临床指征明确时每4周给药一次,而非最初建议的每8周给药一次。所使用的剂量对疗效和成本有影响,但美国实际使用剂量的数据尚不存在。本研究评估英夫利昔单抗治疗的RA患者的剂量及剂量增加率。

方法

研究1:回顾得克萨斯州达拉斯市15名风湿病学家所在的2个大型风湿病诊疗机构中394例RA患者的病历和输液记录。研究2:对1324例使用英夫利昔单抗并参与RA结局纵向研究的RA患者进行调查。患者完成了一份关于临床状况和英夫利昔单抗使用情况的详细问卷。

结果

两项研究结果相似:英夫利昔单抗平均剂量为5mg/kg,在第一年年底前增加最快,此后增速放缓。研究1中61%的患者剂量增加>3mg/kg,研究2中为56%。几乎普遍采用8周的治疗间隔,超过95%的输液在此间隔内进行。剂量增加的最常见原因是反应不足。在完成4次输液的患者中,75%在英夫利昔单抗开始治疗2年后仍在接受治疗。健康评估问卷残疾评分的平均改善为0.28。

结论

英夫利昔单抗剂量增加很常见,尤其是在治疗的第一年。平均剂量为5mg/kg。75%的患者在治疗开始2年后继续使用英夫利昔单抗。

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