Vincristine treatment in steroid-dependent nephrotic syndrome
Vincristine treatment in steroid-dependent nephrotic syndrome
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DOI:
10.1007/s00467-005-1940-7
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发表时间:
2005-10-01
影响因子:
3
通讯作者:
Powell, HR
中科院分区:
文献类型:
--
作者:
Kausman, J;Yin, L;Powell, HR
Treatment of children with steroid-dependent nephrotic syndrome (SDNS) continues to be a challenge when relapses recur after treatment with cyclophosphamide and side effects or non-compliance make steroids and cyclosporin unsatisfactory. We treated 12 patients with intravenous vincristine for SDNS in a regime of 1-1.5 mg/m(2) weekly for 4 weeks then monthly for 4 months. Four of the 5 patients in relapse when commencing vincristine remitted within 2 doses. Comparing relapse frequency in the 12 months before and after vincristine, there was a reduction from 4 to 1.5 (p=0.004) relapses per year. Median sustained remission was 5 months, but 1 frequently relapsing patient remains in remission 4 years after vincristine. Vincristine was also successfully used in 1 or 2 doses at weekly intervals for subsequent relapses in 5 patients. Side effects were minimal in most cases. Abdominal pain occurred in 2 patients who commenced vincristine at 1.5 mg/m(2), but resolved when continued at 1 mg/m(2). We felt vincristine had a role in a subset of children with challenging SDNS administered as 1 mg/m(2) weekly for 4 weeks then 1.5 mg/m(2) monthly for 4 months. Vincristine allowed steroid- and cyclosporin-sparing, contributed to long-term remission in some patients, and was especially valuable in children with poor compliance with oral medication. Many patients expressed a preference for a few doses of vincristine rather than a standard course of oral prednisolone or cyclosporin.