Immune anaemias in patients with chronic lymphocytic leukaemia treated with fludarabine, cyclophosphamide and rituximab - incidence and predictors

被引:61
作者
Borthakur, Gautam [1 ]
O'Brien, Susan [1 ]
Wierda, William G. [1 ]
Thomas, Deborah A. [1 ]
Cortes, Jorge E. [1 ]
Giles, Francis J. [1 ]
Kantarjian, Hagop M. [1 ]
Lerner, Susan [1 ]
Keating, Michael J. [1 ]
机构
[1] MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77030 USA
关键词
immune anaemia; autoimmune haemolytic anaemia; chronic lymphocytic leukaemia;
D O I
10.1111/j.1365-2141.2007.06513.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Immune anaemias (IA) [auto-immune haemolytic anaemia (AIHA) and pure red cell aplasia (PRCA)] are complications of chronic lymphocytic leukaemia (CLL). Fludarabine has been associated with AIHA, whereas both rituximab and cyclophosphamide have been used to treat this condition. Combining these agents with fludarabine may reduce the likelihood of AIHA. We report on the incidence, outcome and pretreatment predictors of IA in 300 patients treated with fludarabine, cyclophosphamide and rituximab (FCR). Nineteen patients (6(.)5%) developed IA [AIHA (5(.)8%), PRCA (0(.)7%)] on or after treatment with FCR. Most patients (82(.)4%) with AIHA had a negative direct antiglobulin test (DAT). Additional markers of haemolysis (indirect hyperbilirubinaemia, reticulocytosis, low haptoglobin and elevated lactate dehydrogenase levels) confirmed the presence of AIHA in these patients. The majority of patients responded to therapies including steroids, ciclosporin, i.v. immunoglobulin, etc. High pretreatment levels of beta-2 microglobulin predicted for development of IA. No haemolytic crisis was observed during FCR therapy in eight patients with AIHA prior to FCR. Thus, the incidence of IA among CLL patients treated with FCR was comparable with historical rates. The diagnosis of AIHA can be considered even if the DAT is negative. Pre-existing AIHA need not preclude front-line FCR therapy.
引用
收藏
页码:800 / 805
页数:6
相关论文
共 39 条
[1]  
[Anonymous], BLOOD
[2]   In vitro production of anti-RBC antibodies and cytokines in chronic lymphocytic leukemia [J].
Barcellini, W ;
Montesano, R ;
Clerici, G ;
Zaninoni, A ;
Imperiali, FG ;
Calori, R ;
Cortelezzi, A ;
Zanella, A .
AMERICAN JOURNAL OF HEMATOLOGY, 2002, 71 (03) :177-183
[3]   Rituximab for primary chronic cold agglutinin disease: a prospective study of 37 courses of therapy in 27 patients [J].
Berentsen, S ;
Ulvestad, E ;
Gjertsen, BT ;
Hjorth-Hansen, H ;
Langholm, R ;
Knutsen, H ;
Ghanima, W ;
Shammas, FV ;
Tjonnfjord, GE .
BLOOD, 2004, 103 (08) :2925-2928
[4]   Salivary and serum β2-microglobulin and gamma-glutamyl-transferase in patients with primary Sjogren syndrome and Sjogren syndrome secondary to systemic lupus erythematosus [J].
Castro, J ;
Jiménez-Alonso, J ;
Sabio, JM ;
Rivera-Cívico, F ;
Martín-Armada, M ;
Rodríguez, MA ;
Jáimez, L ;
Castillo, MJ ;
Sánchez-Román, J .
CLINICA CHIMICA ACTA, 2003, 334 (1-2) :225-231
[5]   National Cancer Institute-sponsored Working Group guidelines for chronic lymphocytic leukemia: Revised guidelines for diagnosis and treatment [J].
Cheson, BD ;
Bennett, JM ;
Grever, M ;
Kay, N ;
Keating, MJ ;
OBrien, S ;
Rai, KR .
BLOOD, 1996, 87 (12) :4990-4997
[6]  
COX DR, 1972, J R STAT SOC B, V34, P187
[7]   Rituximab therapy for chronic lymphocytic leukemia-associated autoimmune hemolytic anemia [J].
D'Arena, Giovanni ;
Laurenti, Luca ;
Capalbo, Silvana ;
D'Arco, Alfonso Maria ;
De Filippi, Rosaria ;
Marcacci, Gianpaolo ;
Di Renzo, Nicola ;
Storti, Sergio ;
Califano, Catello ;
Vigliotti, Maria Luigia ;
Tarnani, Michela ;
Ferrara, Felicetto ;
Pinto, Antonio .
AMERICAN JOURNAL OF HEMATOLOGY, 2006, 81 (08) :598-602
[8]  
Diehl LF, 1998, SEMIN ONCOL, V25, P80
[9]  
DIRAIMONDO F, 1993, LEUKEMIA LYMPHOMA, V11, P63
[10]   Extracellular processing and presentation of a 69-mer synthetic polypeptide to MHC class I-restricted T cells [J].
Eberl, G ;
Renggli, J ;
Men, Y ;
Roggero, MA ;
Lopez, JA ;
Corradin, G .
MOLECULAR IMMUNOLOGY, 1999, 36 (02) :103-112