Long-term follow-up of idiopathic thrombotic thrombocytopenic purpura treated with rituximab

被引:36
作者
Chemnitz, Jens Marcus [1 ,2 ]
Uener, Jens [2 ]
Hallek, Michael [2 ]
Scheid, Christof [2 ]
机构
[1] Univ Hosp Cologne, Dept Internal Med, D-50937 Cologne, Germany
[2] Univ Cologne, Dept Internal Med 1, Cologne, Germany
关键词
TTP; Treatment; Rituximab; Follow-up; VON-WILLEBRAND-FACTOR; HEMOLYTIC-UREMIC SYNDROME; FACTOR-CLEAVING PROTEASE; ANTIBODIES; DISORDERS; ADAMTS13; SURVIVAL; THERAPY;
D O I
10.1007/s00277-010-0968-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Rituximab may be used to treat patients with thrombotic thrombocytopenic purpura (TTP) refractory to plasma exchange or recurrent disease. While initial response rates are reported to be high, long-term follow-up data of patients treated with rituximab are not available to date, however important to estimate the safety and benefit of this treatment. Twelve patients with non-familial idiopathic TTP refractory to plasma exchange or with recurrent disease treated with rituximab between 2000 and 2008 were reexamined. The median follow-up was 49.6 months, ranging from 11 to 97 months. All patients achieved initial complete remission after application of rituximab. During follow-up, nine patients remained disease-free and three patients suffered from recurrent disease. All patients with recurrent disease responded to subsequent rituximab therapy. No long-term side effects were noted during the follow-up period. In conclusion, rituximab represents an effective second-line treatment option in relapsing or refractory TTP. Still, patients need to be closely monitored for relapses with extended follow-up.
引用
收藏
页码:1029 / 1033
页数:5
相关论文
共 25 条
[1]   IMPROVED SURVIVAL IN THROMBOTIC THROMBOCYTOPENIC PURPURA HEMOLYTIC UREMIC SYNDROME - CLINICAL-EXPERIENCE IN 108 PATIENTS [J].
BELL, WR ;
BRAINE, HG ;
NESS, PM ;
KICKLER, TS .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (06) :398-403
[2]   Rituximab as pre-emptive treatment in patients with thrombotic thrombocytopenic purpura and evidence of anti-ADAMTS13 autoantibodies [J].
Bresin, Elena ;
Gastoldi, Sara ;
Daina, Erica ;
Belotti, Daniela ;
Pogliani, Enrico ;
Perseghin, Paolo ;
Scalzulli, Potito R. ;
Paolini, Rossella ;
Marceno, Raimondo ;
Remuzzi, Giuseppe ;
Galbusera, Miriam .
THROMBOSIS AND HAEMOSTASIS, 2009, 101 (02) :233-238
[3]   Successful treatment of severe thrombotic thrombocytopenic purpura with the monoclonal antibody rituximab [J].
Chemnitz, J ;
Draube, A ;
Scheid, C ;
Staib, P ;
Schulz, A ;
Diehl, V ;
Söhngen, D .
AMERICAN JOURNAL OF HEMATOLOGY, 2002, 71 (02) :105-108
[4]   The effect of rituximab on humoral and cell mediated immunity and infection in the treatment of autoimmune diseases [J].
Cooper, Nichola ;
Arnold, Donald M. .
BRITISH JOURNAL OF HAEMATOLOGY, 2010, 149 (01) :3-13
[5]   Efficiency of curative and prophylactic treatment with rituximab in ADAMTS 13-deficient thrombotic thrombocytopenic purpura:: a study of 11 cases [J].
Fakhouri, F ;
Vernant, JP ;
Veyradier, A ;
Wolf, M ;
Kaplanski, G ;
Binaut, R ;
Rieger, M ;
Scheiflinger, F ;
Poullin, P ;
Deroure, B ;
Delarue, R ;
Lesavre, P ;
Vanhille, P ;
Hermine, O ;
Remuzzi, G ;
Grünfeld, JP .
BLOOD, 2005, 106 (06) :1932-1937
[6]   Deficient activity of von Willebrand factor-cleaving protease in chronic relapsing thrombotic thrombocytopenic purpura [J].
Furlan, M ;
Robles, R ;
Solenthaler, M ;
Wassmer, M ;
Sandoz, P ;
Lammle, B .
BLOOD, 1997, 89 (09) :3097-3103
[7]   Von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome [J].
Furlan, M ;
Robles, R ;
Galbusera, M ;
Remuzzi, G ;
Kyrle, PA ;
Brenner, B ;
Krause, M ;
Scharrer, I ;
Aumann, V ;
Mittler, U ;
Solenthaler, M ;
Lämmle, B .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (22) :1578-1584
[8]   Partial purification and characterization of a protease from human plasma cleaving von Willebrand factor to fragments produced by in vivo proteolysis [J].
Furlan, M ;
Robles, R ;
Lammle, B .
BLOOD, 1996, 87 (10) :4223-4234
[9]   Rituximab in the treatment of autoimmune haematological disorders [J].
Garvey, Bernadette .
BRITISH JOURNAL OF HAEMATOLOGY, 2008, 141 (02) :149-169
[10]   How I treat patients with thrombotic thrombocytopenic purpura-hemolytic uremic syndrome [J].
George, JN .
BLOOD, 2000, 96 (04) :1223-1229