Long-term follow-up after rituximab for steroid-dependent idiopathic nephrotic syndrome

被引:112
作者
Kemper, Markus J. [1 ]
Gellermann, Jutta [2 ]
Habbig, Sandra [3 ]
Krmar, Rafael T. [4 ]
Dittrich, Katalin [5 ]
Jungraithmayr, Therese [6 ]
Pape, Lars [7 ]
Patzer, Ludwig [8 ]
Billing, Heiko [9 ]
Weber, Lutz [10 ]
Pohl, Martin [11 ]
Rosenthal, Katrin [12 ]
Rosahl, Anne [1 ]
Mueller-Wiefel, Dirk E. [1 ]
Doetsch, Joerg [3 ]
机构
[1] Univ Childrens Hosp, Hamburg, Germany
[2] Univ Childrens Hosp, Berlin, Germany
[3] Dept Paediat & Adolsecent Med, Cologne, Germany
[4] Karolinska Univ Hosp, Univ Childrens Hosp, Stockholm, Sweden
[5] Univ Childrens Hosp, Erlangen, Germany
[6] Univ Childrens Hosp, Innsbruck, Austria
[7] Univ Childrens Hosp, Hannover, Germany
[8] St Elisabeth & Barabara Childrens Hosp, Halle, Germany
[9] Univ Childrens Hosp, Heidelberg, Germany
[10] Univ Childrens Hosp, Munich, Germany
[11] Univ Childrens Hosp, Freiburg, Germany
[12] Klinikum Nurnberg, Childrens Hosp, Nurnberg, Germany
关键词
nephrotic syndrome; rituximab; steroid sensitive; MYCOPHENOLATE-MOFETIL; T-CELL; CYCLOSPORINE; RESISTANT; CHILDREN;
D O I
10.1093/ndt/gfr548
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Background. In patients with refractory steroid-sensitive nephrotic syndrome (SSNS), treatment with rituximab has shown encouraging results; however, long-term follow-up data are not available. Methods. We performed a retrospective analysis of 37 patients (25 boys) with steroid-dependent nephrotic syndrome who were treated with rituximab (375 mg/m(2) given weekly for one to four courses). Long-term follow-up data (>2 years, median 36, range 24-92.8 months) are available for 29 patients (12 boys). Results. Twenty-six of 37 (70.3%) patients remained in remission after 12 months. Relapses occurred in 24 (64.8%) patients after a median of 9.6 (range 5.2-64.1) months. Time to first relapse was significantly shorter in patients receiving one or two compared to three or four initial infusions. In the 29 patients with long-term follow-up for >2 years, 12 (41%) patients remained in remission after the initial rituximab course for >24 months, 7 (24.1%) patients without further maintenance immunosuppression. Nineteen children received two to four repeated courses of rituximab increasing the total number of patients with long-term remission to 20 (69%), remission including 14 (48%) patients off immunosuppression. The proportion of patients with long-term remission was not related to the number of initial rituximab applications. No serious side effects were noted. Conclusion. Rituximab is an effective treatment option in the short- and long-term control of treatment refractory SSNS. Further controlled studies are needed to address optimal patient selection, dose and safety of rituximab infusions.
引用
收藏
页码:1910 / 1915
页数:6
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