Retrospective multicenter study on the development of peripheral lymphocytosis following second-line dasatinib therapy for chronic myeloid leukemia

被引:23
|
作者
Lee, Su Jin [7 ]
Jung, Chul Won [7 ]
Kim, Dae-Young [2 ,7 ]
Lee, Kyoo-Hyung [2 ,7 ]
Sohn, Sang Kyun [3 ,7 ]
Kwak, Jae-Yong [4 ,7 ]
Kim, Hyeoung-Joon [5 ,7 ]
Kim, In Ho [6 ,7 ]
Park, Seonyang [6 ,7 ]
Kim, Dong Hwan [1 ,7 ]
机构
[1] Sungkyunkwan Univ, Sch Med, Div Hematol Oncol, Dept Med,Samsung Med Ctr, Seoul 135710, South Korea
[2] Asan Med Ctr, Dept Internal Med, Seoul, South Korea
[3] Kyungpook Natl Univ Hosp, Dept Hematol Oncol, Taegu, South Korea
[4] Chonbuk Natl Univ Hosp, Div Hematol Oncol, Jeonju, South Korea
[5] Chonnam Natl Univ Hwasun Hosp, Dept Hematol Oncol, Hwasun, South Korea
[6] Seoul Natl Univ Hosp, Dept Internal Med, Seoul 110744, South Korea
[7] Korean Soc Hematol CML Working Party, Seoul, South Korea
关键词
TYROSINE KINASE INHIBITOR; IMATINIB-RESISTANT; CYTOGENETIC RESPONSES; FAILURE; TARGET; CELLS;
D O I
10.1002/ajh.21980
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The current retrospective study investigated the incidence of lymphocytosis following second-line dasatinib therapy in chronic myeloid leukemia (CML) and analyzed the clinical factors predictive of the development of lymphocytosis, as well as association with treatment outcomes. Fifty CML patients who failed imatinib treatment and received dasatinib were included from nine centers in the Republic of Korea. The cumulative incidence of lymphocytosis was assessed, and cytogenetic and molecular response, treatment failure, loss of response, progression to advanced disease, and survival were evaluated and analyzed according to the development of lymphocytosis. After a median of 17 months of dasatinib therapy, 23 patients (46%) developed lymphocytosis (median onset 4 months). No clinical predictive factor for the development of lymphocytosis was found. The group presenting lymphocytosis showed a higher complete cytogenetic response (CCyR; 78.3 vs. 29.6%, P = 0.001) and major molecular response (MMR; 52.2 vs. 14.8%, P = 0.005), in comparison to the group without presenting lymphocytosis. The development of lymphocytosis after dasatinib was identified as a favorable independent marker for predicting a CCyR (P = 0.002) or MMR (P = 0.003). Further study is necessary to identify which subset of lymphocytes was expanded and to reveal the exact mechanism by which dasatinib induces lymphocyte expansion. Am. J. Hematol. 86:346-350, 2011. (C) 2011 Wiley-Liss, Inc.
引用
收藏
页码:346 / 350
页数:5
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