High response rate and durable remissions following fludarabine and rituximab combination therapy for chronic cold agglutinin disease

被引:122
作者
Berentsen, Sigbjorn [1 ]
Randen, Ulla [2 ]
Vagan, Anne Marita [3 ]
Hjorth-Hansen, Henrik [4 ,5 ]
Vik, Anders [6 ]
Dalgaard, Jakob [7 ]
Jacobsen, Eva-Marie [8 ,9 ]
Thoresen, Aud S. [10 ]
Beiske, Klaus [2 ]
Tjonnfjord, Geir E. [8 ,9 ]
机构
[1] Haugesund Hosp, Dept Med, N-5504 Haugesund, Norway
[2] Oslo Univ Hosp, Dept Pathol, Oslo, Norway
[3] Alesund Hosp, Dept Internal Med, Alesund, Norway
[4] Univ Trondheim Hosp, St Olavs Hosp, Dept Hematol, Trondheim, Norway
[5] Norwegian Univ Sci & Technol NTNU, Dept Canc Res & Mol Med, Trondheim, Norway
[6] Univ Hosp N Norway, Dept Med, Tromso, Norway
[7] Hosp Buskerud, Dept Med, Drammen, Norway
[8] Oslo Univ Hosp, Dept Hematol, Oslo, Norway
[9] Univ Oslo, Inst Clin Med, Oslo, Norway
[10] Innlandet Hosp Trust Gjovik, Dept Med, Gjovik, Norway
关键词
AUTOIMMUNE-DISEASE; LOW-GRADE; HEMOLYSIS; MECHANISMS; UPDATE;
D O I
10.1182/blood-2010-06-288647
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Most patients diagnosed with primary chronic cold agglutinin disease (CAD) have a clonal lymphoproliferative bone marrow disorder. Treatment with rituximab is the only well-documented effective therapy, leading to 45%-60% partial responses (PR). Complete responses (CR) are rare, and median response duration is only 11 months. In a prospective multicenter trial, 29 patients received rituximab 375 mg/m(2) on days 1, 29, 57 and 85; and fludarabine orally, 40 mg/m(2) on days 1-5, 29-34, 57-61 and 85-89. Twenty-two patients (76%) responded, 6 (21%) achieving CR and 16 (55%) PR. Among 10 patients nonresponsive to rituximab monotherapy, 1 achieved CR and 6 PR. Median increase in hemoglobin level was 3.1 g/dL among the responders and 4.0 g/dL in those who achieved CR. Lower quartile of response duration was not reached after 33 months. Estimated median response duration was more than 66 months. Grade 3-4 hematologic toxicity occurred in 12 patients (41%). In conclusion, fludarabine and rituximab combination therapy is very efficient in patients with CAD. Toxicity may be a concern, and benefits should be carefully weighed against risks in very old and comorbid patients. It remains to be established whether the combination should be first-line or an efficient second-line therapy in CAD patients requiring treatment. This study is registered at http://www.clinicaltrials.gov as NCT00373594. (Blood. 2010; 116(17): 3180-3184)
引用
收藏
页码:3180 / 3184
页数:5
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