Pulse cyclophosphamide for steroid-resistant focal segmental glomerulosclerosis

被引:30
作者
Rennert, WP [1 ]
Kala, UK [1 ]
Jacobs, D [1 ]
Goetsch, S [1 ]
Verhaart, S [1 ]
机构
[1] Univ Witwatersrand, Baragwanath Hosp, Dept Pediat, ZA-2013 Johannesburg, South Africa
关键词
focal segmental glomerulosclerosis; steroid resistant; intravenous pulse cyclophosphamide;
D O I
10.1007/s004670050574
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
We report the response of ten patients (6 male, 4 female) with steroid-resistant focal segmental glomerulosclerosis (FSGS) to treatment with intravenous pulse cyclophosphamide (IVCP) together with oral prednisone. All patients had been treated with 60 mg/m(2) oral prednisone daily for 2 months upon initial presentation. IVCP was given monthly at a dose of 500 mg/m(2) over 6 months. Oral prednisone was given concurrently at 60 mg/m(2) daily for 2 months and then on alternate days for 4 months, followed by 30 mg/m(2) on alternate days for 6 months. Prednisone was then tapered monthly by 10 mg and finally discontinued. Five patients failed to respond to steroids from the onset and were considered as primary steroid resistant. Two of these patients achieved sustained remission after IVCP, one patient showed a partial response, with loss of edema, normalization of serum albumin, and persistent proteinuria, while two patients showed no response to IVCP. The other five patients had achieved remission after 2 months of daily prednisone at 60 mg/m(2) upon initial presentation, but had suffered from more than three relapses per year and had eventually become steroid resistant. They were considered secondary steroid resistant. All five patients achieved sustained remission after IVCP. None of our patients suffered from adverse effects of IVCP. The suggest IVCP as an adjunctive therapy for steroid-resistant FSGS, particularly for patients with secondary steroid resistance.
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页码:113 / 116
页数:4
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