The effect of imatinib therapy on the outcome of allogeneic stem cell transplantation in adults with Philadelphia chromosome-positive acute lymphoblastic leukemia

被引:23
作者
Zhang, Fu-Hua [1 ]
Ling, Yi-Wen [2 ]
Zhai, Xiao [1 ]
Zhang, Yu [1 ]
Huang, Fen [1 ]
Fan, Zhi-Ping [1 ]
Zhou, Hong-Sheng [1 ]
Jiang, Qian-Li [1 ]
Sun, Jing [1 ]
Liu, Qi-Fa [1 ]
机构
[1] Southern Med Univ, Nanfang Hosp, Dept Hematol, Guangzhou 510515, Guangdong, Peoples R China
[2] Southern Med Univ, Nanhai Hosp, Dept Hematol, Foshan, Peoples R China
关键词
Philadelphia chromosome; Acute lymphocytic leukemia; Allogeneic hematopoietic stem cell transplantation; TYROSINE KINASE INHIBITORS; BONE-MARROW-TRANSPLANTATION; T-CELLS; PROGNOSIS; DISEASE;
D O I
10.1179/1607845412Y.0000000052
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To evaluate the efficacy of imatinib administration before and/or after allogeneic hematopoietic stem cell transplantation (allo-HSCT) for patients with Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL). Method: Patients with imatinib therapy time exceeding 30 days pre-/post-transplant were screened in our data. Imatinib was used in induced or consolidated chemotherapy pre-transplant, or maintenance therapy after 60 days post-transplant (therapy time was less than 180 days) regardless of the molecular status of the disease. Results: Sixty-nine patients with Ph+ ALL were enrolled in the retrospective analysis. Forty-four patients received imatinib therapy, including 24 pre-transplant, 9 post-transplant, and 11 both pre- and post-transplant. With a median follow-up time of 395 days (range, 55-2762 days) post-transplant, 3-year estimated overall survival was 62.3 +/- 16.6, 40.0 +/- 21.9, 41.7 +/- 22.2, and 25.9 +/- 11.4%, respectively (P = 0.221), and disease-free survival (DFS) was 53.6 +/- 17.9, 20.0 +/- 17.9, 33.3 +/- 25.5% and 23.6 +/- 11.4%, respectively (P = 0.421), in patients with imatinib therapy pre- transplant, post-transplant, both pre- and post-transplant, neither pre- nor post-transplant. The incidence of relapse at 3 year for patients with imatinib therapy post-transplant (n = 20) was 63.6%, comparing with 24.2% (P = 0.018) in patients without imatinib therapy post-transplant (n = 49). The ratio of CD4+CD25+Foxp3+ cells in blood was significantly higher at 30 and 60 days after imatinib therapy than that at the time of pre- imatinib in 20 patients (P = 0.019 and 0.001, respectively). Conclusions: Application of imatinib pre- transplant might have benefited for patients with Ph+ ALL. Whether administration of imatinib, regardless of the molecular status of the disease post-transplant increases relapse, is a worthy goal for further study.
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收藏
页码:151 / 157
页数:7
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