Current Status and Perspectives of Tyrosine Kinase Inhibitor Treatment in the Posttransplant Period in Patients with Chronic Myelogenous Leukemia (CML)

被引:30
作者
Klyuchnikov, Evgeny [1 ]
Kroeger, Nicolaus [1 ]
Brummendorf, Tim H. [2 ]
Wiedemann, Bettina [1 ]
Zander, Axel Rolf [1 ]
Bacher, Ulrike [1 ]
机构
[1] UCCH, Interdisciplinary Clin Stem Cell Transplantat, D-20246 Hamburg, Germany
[2] Univ Aachen, Dept Hematol & Oncol, Aachen, Germany
关键词
Allogeneic stem cell transplantation (SCT); Chronic myelogenous leukemia (CML); Tyrosine kinase inhibitors (TKIs); Imatinib; Dasatinib; CHRONIC MYELOID-LEUKEMIA; STEM-CELL TRANSPLANTATION; IMATINIB MESYLATE THERAPY; HIGH-DOSE IMATINIB; BCR-ABL MUTATIONS; DONOR LYMPHOCYTE INFUSIONS; ALLOGENEIC TRANSPLANTATION; MOLECULAR REMISSION; PERIPHERAL-BLOOD; DOMAIN MUTATIONS;
D O I
10.1016/j.bbmt.2009.08.019
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Following the introduction of tyrosine kinase inhibitors (TKIs) in chronic myelogenous leukemia (CML), allogeneic stem cell transplantation (SCT) took a shift toward high-risk patients. Considering the high relapse rates posttransplant in these selected patients, several studies evaluated posttransplant use of the TKI imatinib. Although the number of studies are still limited, and data have to be confirmed by additional studies, safety of imatinib even within the first months after SCT seems to be acceptable. Imatinib was shown to be effective in patients with molecular or hematologic relapse of chronic or accelerated phase posttransplant (CP, AP), whereas outcomes in blast phase were more unfavorable. The compound further seemed beneficial for prophylactic use in patients who achieved complete remission posttransplant. The combination of imatinib with donor lymphocytes did not result in increased toxicity or graft-versus-host disease (GVHD). First studies suggest that second-generation TKIs such as dasatinib or nilotinib are manageable posttransplant with acceptable toxicity as well. In conclusion, TKIs of the first- and second-generation are promising options for the posttransplant period of patients with CML, but algorithms for dosage, intervals from SCT, duration of application, and the combination with donor lymphocytes still have to be developed. Biol Blood Marrow Transplant 16: 301-310 (2010) (C) 2010 American Society for Blood and Marrow Transplantation
引用
收藏
页码:301 / 310
页数:10
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