Fludarabine with cytarabine followed by reduced-intensity conditioning and allogeneic hematopoietic stem cell transplantation in patients with poor-risk chronic lymphocytic leukemia

被引:7
|
作者
Krejci, Marta [1 ]
Doubek, Michael [1 ,2 ]
Brychtova, Yvona [1 ]
Stehlikova, Olga [1 ]
Chovancova, Jana [1 ]
Tichy, Boris [1 ,2 ]
Francova, Hana Skuhrova [1 ]
Navratil, Milan [1 ]
Tomiska, Miroslav [1 ]
Horky, Ondrej [1 ]
Pospisilova, Sarka [1 ,2 ]
Mayer, Jiri [1 ,2 ]
机构
[1] Univ Hosp Brno, Dept Internal Med Hematol & Oncol, Brno 62500, Czech Republic
[2] Masaryk Univ, Cent European Inst Technol, Brno 62500, Czech Republic
关键词
Chronic lymphocytic leukemia; Reduced-intensity conditioning; Fludarabine; Cytarabine; ACUTE MYELOID-LEUKEMIA; RESIDUAL DISEASE; CHEMOTHERAPY; PROPHYLAXIS; GUIDELINES; SURVIVAL;
D O I
10.1007/s00277-012-1579-y
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Allogeneic stem cell transplantation (SCT) is a treatment option for patients with poor-risk chronic lymphocytic leukemia (CLL). Sequential use of chemotherapy and reduced-intensity conditioning has been proposed to improve the treatment outcomes. Fludarabine (30 mg/m(2)/day) and cytarabine (2 g/m(2)/day) for 4 days (combination of fludarabine with cytarabine; FAraC) were used for cytoreduction. After 3 days of rest, reduced intensity conditioning (RIC) was carried out consisting of 4 Gy total body irradiation, 10-20 mg/kg/day antithymocyte globulin for 3 days, and 40-60 mg/kg/day cyclophosphamide for 2 days. The median time of neutrophil engraftment was 16 days. The most frequent toxicities were grades III/IV infections in 12 of 15 cases and gastrointestinal toxicities in 8 of 15 cases. Remission (complete remission + partial remission) was achieved in 14 of 15 patients (93 %), minimal residual disease negativity according to flowcytometric analysis was observed in 10 patients. Nonrelapse mortality after 1 and 2 years was 7 and 13 %, respectively. After the median follow-up from SCT of 30 months, 80 % of patients were alive (12/15), three patients have died, and three relapses occurred. The FAraC-RIC protocol seems to be a promising approach to the treatment of poor-risk CLL with a high response rate of 93 % and favorable progression-free survival and overall survival of 70 and 85 % at 2 years after SCT, respectively. Other prospective clinical trials are needed to confirm the results of this novel therapeutic strategy.
引用
收藏
页码:249 / 254
页数:6
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