Long-Term Prognosis of Adult Patients with Steroid-Dependent Minimal Change Nephrotic Syndrome Following Rituximab Treatment

被引:38
作者
Iwabuchi, Yuko [1 ]
Takei, Takashi [1 ]
Moriyama, Takahito [1 ]
Itabashi, Mitsuyo [1 ]
Nitta, Kosaku [1 ]
机构
[1] Tokyo Womens Med Univ, Dept Med, Kidney Ctr, Tokyo 1628666, Japan
关键词
CHILDREN;
D O I
10.1097/MD.0000000000000300
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This study was to evaluate the long-term efficacy and safety of a single-dose rituximab regimen rituximab treatment in adult patients with steroid-dependent minimal change nephrotic syndrome (MCNS). We conducted a prospective cohort study with historical controls to evaluate the effect of single-dose infusions of rituximab at 375 mg/m(2) BSA per dose administered at intervals of 6 months for a period of 24 months. At the end of the 24-month period, the patients were divided into the treatment continuation (n = 20) and treatment discontinuation (n = 5) groups according to their intention to continue/discontinue the treatment. A significant reduction in the total number of relapses was observed during the 24-month period after the first rituximab infusion as compared with that during the 24-month period before the first rituximab infusion (108 vs. 8, P < 0.001). Complete remission was induced/maintained in all patients from 12 to 24 months after the first rituximab infusion. In regard to the clinical course after 24 months, 4 of the 20 patients in the treatment continuation group discontinued the rituximab treatment after the fifth infusion and 2 patients discontinued the treatment after the sixth infusion. However, complete remission was maintained in all the 20 patients of this group during the 12-month observation period after the first four single-dose rituximab infusions. On the other hand, 1 of the 5 patients in the treatment discontinuation group developed relapse during the observation period after the first four rituximab infusions, and the rituximab treatment was resumed. In our trial, rituximab therapy was associated with maintenance of complete remission. Complete remission was maintained even in most of the patients who showed B-cell repletion after discontinuation of rituximab therapy. Thus, rituximab may be considered as a radical therapeutic agent for patients with steroid-dependent MCNS.
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共 23 条
[11]   Rituximab for childhood-onset, complicated, frequently relapsing nephrotic syndrome or steroid-dependent nephrotic syndrome: a multicentre, double-blind, randomised, placebo-controlled trial [J].
Iijima, Kazumoto ;
Sako, Mayumi ;
Nozu, Kandai ;
Mori, Rintaro ;
Tuchida, Nao ;
Kamei, Koichi ;
Miura, Kenichiro ;
Aya, Kunihiko ;
Nakanishi, Koichi ;
Ohtomo, Yoshiyuki ;
Takahashi, Shori ;
Tanaka, Ryojiro ;
Kaito, Hiroshi ;
Nakamura, Hidefumi ;
Ishikura, Kenji ;
Ito, Shuichi ;
Ohashi, Yasuo .
LANCET, 2014, 384 (9950) :1273-1281
[12]   Single dose of rituximab for refractory steroid-dependent nephrotic syndrome in children [J].
Kamei, Koichi ;
Ito, Shuichi ;
Nozu, Kandai ;
Fujinaga, Shuichiro ;
Nakayama, Makiko ;
Sako, Mayumi ;
Saito, Mari ;
Yoneko, Maki ;
Iijima, Kazumoto .
PEDIATRIC NEPHROLOGY, 2009, 24 (07) :1321-1328
[13]   Long-term follow-up after rituximab for steroid-dependent idiopathic nephrotic syndrome [J].
Kemper, Markus J. ;
Gellermann, Jutta ;
Habbig, Sandra ;
Krmar, Rafael T. ;
Dittrich, Katalin ;
Jungraithmayr, Therese ;
Pape, Lars ;
Patzer, Ludwig ;
Billing, Heiko ;
Weber, Lutz ;
Pohl, Martin ;
Rosenthal, Katrin ;
Rosahl, Anne ;
Mueller-Wiefel, Dirk E. ;
Doetsch, Joerg .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2012, 27 (05) :1910-1915
[14]   Cyclosporine-A-induced nephrotoxicity in children with minimal-change nephrotic syndrome:: long-term treatment up to 10 years [J].
Kranz, Birgitta ;
Vester, Udo ;
Buescher, Rainer ;
Wingen, Anne-Margret ;
Hoyer, Peter F. .
PEDIATRIC NEPHROLOGY, 2008, 23 (04) :581-586
[15]   Reconstitution of peripheral blood B cells after depletion with rituximab in patients with rheumatoid arthritis [J].
Leandro, MJ ;
Cambridge, G ;
Ehrenstein, MR ;
Edwards, JCW .
ARTHRITIS AND RHEUMATISM, 2006, 54 (02) :613-620
[16]  
Maloney DG, 1997, BLOOD, V90, P2188
[17]   GSTT1 gene abnormality in minimal change nephrotic syndrome with elevated serum immunoglobulin E [J].
Miyazaki, Kohei ;
Sugimoto, Keisuke ;
Tsuji, Shoji ;
Iharada, Anna ;
Fujita, Shinsuke ;
Yanagida, Hidehiko ;
Sakata, Naoki ;
Okada, Mitsuru ;
Kaneko, Kazunari ;
Takemura, Tsukasa .
CLINICAL NEPHROLOGY, 2012, 77 (04) :261-266
[18]   Rituximab is an efficient and safe treatment in adults with steroid-dependent minimal change disease [J].
Munyentwali, Helene ;
Bouachi, Khedidja ;
Audard, Vincent ;
Remy, Philippe ;
Lang, Philippe ;
Mojaat, Rachid ;
Deschenes, Georges ;
Ronco, Pierre M. ;
Plaisier, Emmanuelle M. ;
Dahan, Karine Y. .
KIDNEY INTERNATIONAL, 2013, 83 (03) :511-516
[19]   CD20: A target antigen for immunotherapy of autoimmune diseases [J].
Perosa, F ;
Favoino, E ;
Caragnano, MA ;
Prete, M ;
Dammacco, F .
AUTOIMMUNITY REVIEWS, 2005, 4 (08) :526-531
[20]   Short-Term Effects of Rituximab in Children with Steroid- and Calcineurin-Dependent Nephrotic Syndrome: A Randomized Controlled Trial [J].
Ravani, Pietro ;
Magnasco, Alberto ;
Edefonti, Alberto ;
Murer, Luisa ;
Rossi, Rossella ;
Ghio, Luciana ;
Benetti, Elisa ;
Scozzola, Floriana ;
Pasini, Andrea ;
Dallera, Nadia ;
Sica, Felice ;
Belingheri, Mirco ;
Scolari, Francesco ;
Ghiggeri, Gian Marco .
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2011, 6 (06) :1308-1315