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临床试验:环磷酰胺脉冲疗法——治疗难治性克罗恩病的有前途的治疗选择。

Clinical trial: cyclophosphamide pulse therapy - a promising therapeutic alternative in refractory Crohn's disease.

机构信息

Department of Internal Medicine I, University Hospital of Schleswig-Holstein, Lübeck, Germany.

出版信息

Aliment Pharmacol Ther. 2009 Jun 15;29(12):1230-9. doi: 10.1111/j.1365-2036.2009.03999.x. Epub 2009 Mar 19.

Abstract

BACKGROUND

In severe steroid-refractory Crohn's disease (CD), established therapies fail in a relevant proportion of patients. Recent pilot studies indicated the efficacy of cyclophosphamide pulse therapy in these patients.

AIM

To provide further and substantial evidence for the rationale to apply cyclophosphamide pulse therapy as therapeutic option in severe courses of CD.

METHODS

Fifteen patients with steroid-refractory (n = 13) or steroid-dependent (n = 2) CD received 2-6 (median 3) monthly pulses of 750 mg cyclophosphamide in an open-label fashion. Eleven patients were on concomitant immunosuppression (azathioprine/mercaptopurine n = 9; methotrexate n = 2).

RESULTS

Thirteen of 15 patients (87%) had a clinical response (CDAI decrease >100). Ten patients (67%) went into remission (CDAI <150) after 8 weeks. Steroid-free remission was achieved in eight patients (54%). Two patients (13%) failed to respond. Median CDAI decreased from 420 (245-550) to 100 (26-538) at week 8. Remission lasted 16 months (median, range 4-40). In three patients, arthritis, erythema nodosum and episcleritis completely resolved. Cyclophosphamide pulse therapy administration was well tolerated in all subjects.

CONCLUSIONS

Cyclophosphamide pulse therapy is safe and highly effective for induction and maintenance of remission in steroid-refractory/-dependent CD. There is a strong need for additional experience to improve the setting of the encouraging cyclophosphamide treatment in CD.

摘要

背景

在严重的激素难治性克罗恩病(CD)中,相当一部分患者的既定治疗方法均失败。最近的试点研究表明环磷酰胺冲击疗法对这些患者有效。

目的

为将环磷酰胺冲击疗法作为 CD 严重病程的治疗选择提供进一步的实质性证据。

方法

15 例激素难治性(n=13)或激素依赖型(n=2)CD 患者接受了 2-6(中位数 3)个疗程的每月环磷酰胺 750mg 冲击治疗,采用开放标签设计。11 例患者同时接受免疫抑制治疗(硫唑嘌呤/巯嘌呤 n=9;甲氨蝶呤 n=2)。

结果

15 例患者中有 13 例(87%)有临床反应(CDAI 下降>100)。10 例患者(67%)在 8 周后进入缓解期(CDAI<150)。8 例患者(54%)实现了无激素缓解。2 例患者(13%)无应答。8 周时 CDAI 中位数从 420(245-550)降至 100(26-538)。缓解持续时间为 16 个月(中位数,范围 4-40)。3 例患者的关节炎、结节性红斑和表层巩膜炎完全缓解。所有患者均能耐受环磷酰胺冲击治疗。

结论

环磷酰胺冲击疗法安全且对激素难治性/依赖性 CD 的诱导和维持缓解非常有效。需要进一步的经验来改善环磷酰胺在 CD 中的治疗设置,以获得更好的效果。

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