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在韦格纳肉芽肿缓解期维持治疗中,口服甲氨蝶呤与来氟米特相比复发率更高。

Elevated relapse rate under oral methotrexate versus leflunomide for maintenance of remission in Wegener's granulomatosis.

作者信息

Metzler C, Miehle N, Manger K, Iking-Konert C, de Groot K, Hellmich B, Gross W L, Reinhold-Keller E

机构信息

Department of Rheumatology, University Hospital of Schleswig-Holstein, Campus Luebeck, Ratzeburger Allee 160, D-23538 Luebeck, Germany.

出版信息

Rheumatology (Oxford). 2007 Jul;46(7):1087-91. doi: 10.1093/rheumatology/kem029. Epub 2007 May 22.

Abstract

OBJECTIVES

Results from open-label trials suggest that methotrexate (MTX) and leflunomide (LEF) are effective for maintenance of remission in Wegener's granulomatosis (WG), but data from randomized controlled clinical trails are not yet available.

METHODS

In this multicentre, prospective randomized controlled clinical trial, patients with generalized WG were treated either with oral LEF 30 mg/day or oral MTX (starting with 7.5 mg/week reaching 20 mg/week after 8 weeks) for 2 yrs following induction of remission with cyclophosphamide. The primary endpoint was the incidence of relapses. Secondary outcome parameters were DEI, BVAS, SF-36, cANCA-titre, ESR and CRP.

RESULTS

Fifty-four patients were included in the study, 26 in the LEF-limb, 28 in the MTX-limb. In the LEF-group, six patients relapsed after a median time of 7 months, thereof one major relapse with a new pulmonary manifestation. In the MTX-group, 13 relapses occurred in 6 months, of which seven were major: rapidly progressive glomerulonephritis (n = 4), pulmonary haemorrhage (n = 2) and one cerebral granuloma. The significantly higher incidence of major relapses in the MTX-limb (P = 0.037) led to premature termination of the study. In the LEF-limb, four patients were withdrawn due to hypertension (n = 2), peripheral neuropathy (n = 1) and leucopenia (n = 1).

CONCLUSION

LEF at a dosage of 30 mg/day appears to be effective in the prevention of major relapses in WG, however, this is associated with an increased frequency of adverse events. Further studies testing other dosing regimens of lower doses of LEF are needed to confirm these promising results in larger patients cohorts.

摘要

目的

开放标签试验结果表明,甲氨蝶呤(MTX)和来氟米特(LEF)对维持韦格纳肉芽肿(WG)缓解有效,但随机对照临床试验的数据尚未可得。

方法

在这项多中心、前瞻性随机对照临床试验中,全身性WG患者在接受环磷酰胺诱导缓解后,接受口服LEF 30毫克/天或口服MTX(起始剂量为7.5毫克/周,8周后增至20毫克/周)治疗2年。主要终点是复发率。次要结局参数包括疾病活动指数(DEI)、伯明翰血管炎活动评分(BVAS)、健康调查简表36(SF - 36)、抗中性粒细胞胞浆抗体(cANCA)滴度、红细胞沉降率(ESR)和C反应蛋白(CRP)。

结果

54例患者纳入研究,来氟米特组26例,甲氨蝶呤组28例。来氟米特组中,6例患者在中位时间7个月后复发,其中1例为伴有新肺部表现的严重复发。甲氨蝶呤组在6个月内发生13次复发,其中7次为严重复发:快速进行性肾小球肾炎(4例)、肺出血(2例)和1例脑肉芽肿。甲氨蝶呤组严重复发的发生率显著更高(P = 0.037),导致研究提前终止。来氟米特组中,4例患者因高血压(2例)、周围神经病变(1例)和白细胞减少(1例)退出研究。

结论

30毫克/天剂量的来氟米特似乎对预防WG的严重复发有效,然而,这与不良事件发生率增加有关。需要进一步研究来测试更低剂量来氟米特的其他给药方案,以在更大患者队列中证实这些有前景的结果。

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