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伊马替尼联合造血干细胞移植治疗慢性粒细胞白血病
引用本文:孟凡义,孙竞,刘启发,徐丹,魏永强,张钰,江千里. 伊马替尼联合造血干细胞移植治疗慢性粒细胞白血病[J]. 白血病.淋巴瘤, 2006, 15(4): 266-268
作者姓名:孟凡义  孙竞  刘启发  徐丹  魏永强  张钰  江千里
作者单位:510515,广州,南方医科大学南方医院血液科;510515,广州,南方医科大学南方医院血液科;510515,广州,南方医科大学南方医院血液科;510515,广州,南方医科大学南方医院血液科;510515,广州,南方医科大学南方医院血液科;510515,广州,南方医科大学南方医院血液科;510515,广州,南方医科大学南方医院血液科
基金项目:广东省社会发展攻关课题资助项目(B30202)
摘    要: 目的 研究伊马替尼(商品名:格列卫)对异基因造血干细胞移植(allo-HSCT)和自体外周血造血干细胞移植(APBSCT)的影响。方法 18例慢性粒细胞白血病(CML)分为2组:①al-lo-HSCT组14例,其中10例为CML加速期(AP)和急变期(BP),4例为CML慢性期(CP),移植之前格列卫疗程中位数为25(7~60)d,供受者HLA完全相合,亲缘相关供者9例、非亲缘供者5例,预处理方案为TBI+Cy+VP16或Bu/Cy±ATG,GVHD预防按常规方案进行;②APBSC动员4例,均为CML-CP患者,格列卫治疗的中位数疗程5.5(4~26)个月,动员前反复IFISH-bcr/abl阳性率0~2%,动员方案CAE+G-CSF,其中3例经TBI+Cy+VP16预处理后进行了APBSCT。结果 4例患者经G-CSF动员第5天分离自体外周血干细胞(APBSC)1次,得CD+34细胞的中位数6.8(3.9~9.6)×106/kg,动员产品中IFISH-bcr/abl阳性细胞比例高于动员前骨髓细胞(2.8 %∶0.8 %),4例动员PBSC的患者中3例进行了APBSCT,移植后随访中位时间24(18~28)个月,2例复发,1例持续IFISH-bcr/abl阴性。14例allo-HSCT患者中位随访8(4~20)个月,造血重建需要8~21 d,发生GVHD 8例,白血病复发2例,移植相关并发症死亡2例,复发死亡1例,无病生存9例。结论 格列卫治疗后对CML患者造血干细胞的动员、移植结果无明显影响。

关 键 词:伊马替尼  造血干细胞移植  慢性粒细胞白血病
文章编号:1009-9921(2006)04-0266-03
收稿时间:2006-10-27;
修稿时间:2006-01-18

Imatinib mesylate combined with hematopiotic stem cell transplantation for chronic myloid leukemia
MENG Fan-yi,SUN Jing,LIU Qi-fa,XU Dan,WEI Yong-qiang,ZHANG Yu,JIANG Qian-li. Imatinib mesylate combined with hematopiotic stem cell transplantation for chronic myloid leukemia[J]. Journal of Leukemia & Lymphoma, 2006, 15(4): 266-268
Authors:MENG Fan-yi  SUN Jing  LIU Qi-fa  XU Dan  WEI Yong-qiang  ZHANG Yu  JIANG Qian-li
Affiliation:Department of Hematoloy, Nanfang Hospital, Southern Medical University
Abstract:Objective To study the effect of imatinib combined with allogenic hematopoietic stem cell transplantation (allo-HSCT) or autologous peripheral blood stem cell transplantation (APBSCT) in chronic myeloid leukemia (CML) patients. Methods 18 CML patients were divided into 2 groups, 14 in group A and 4 in group B. Patients in group A undergone allo-HSCT, 10 were in CML accelerating phase or blast crisis, 4 were in chronic phase; among 14 patients, the median period of imatinib treatment before allo-HSCT was 25 d (7 ~ 60 d), 9 had related complete HLA-matched donors and 5 had unrelated complete matched donors, the regimen was TBI+Cy+VP16 or Bu/Cy±ATG, routine protocol to prevent graft versus host disease (GVHD). Patients in group B were all in chronic phase, the median period of imatinib treatment before APBSCT was 5.5 months (4 ~ 26 d), repeated negative detection of bcr/abl by IFISH, mobilization protocol was CAE+G-CSF, 3 of 4 undergone TBI+Cy+VP16 followed by APBSCT. Results In group B, 4 patients were harvested PBSC on d 5 of G-CSF mobilization, (3.9 ~ 9.6)×106/kg CD+34 cells were obtained, however, IFISH-bcr/abl postive cells in separation products increased from 0.8 % to 2.8 %. Median follow-up period after transplantation is 24 (18 ~ 28) months, 2 cases relapsed, 1 case remains IFISH-bcr/abl negative. In group A, 8 of 14 cases had GVHD, median follow-up period after transplantation is 8 (4 ~ 20) months, 2 cases relapsed, 2 cases died of trans-plantation-related complications, 1 case died of relapse, 9 cases remain disease free. Among 14 patients, hematopoietic reconstitution was on 8 ~ 21 days after transplantation. Conclusion No obvious effect of ima-tinib on the results of mobiligation and outcome of the hematopoietic stem cell transplantation in CML pa-tients.
Keywords:Imatinib  Hematopiotic stem cell transplantation  Chronic myloid leukemia
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