He Yi, Feng Si-zhou, Wang Mei, Wei Jia-lin, Qin Tie-jun, Zhou Zheng, Zhai Wen-jing, Qiu Lu-gui, Han Ming-zhe
Institute of Hematology and Blood Diseases Hospital, CAMS & PUMC, Tianjin 300020, China.
Zhonghua Xue Ye Xue Za Zhi. 2005 Jul;26(7):389-92.
To evaluate the treatment outcome of HLA-identical sibling allogeneic hematopoietic stem cell transplantation (allo-HSCT) for chronic myelogenous leukemia (CML) patients in first chronic phase (CP(1)).
Fifty-one patients with CML-CP(1) received HLA-identical sibling allo-HSCT with conditioning regimens of TBI plus Cy or Bu plus Cy. Allogeneic peripheral blood stem cell transplantation (PBSCT) and bone marrow transplantation (BMT) were performed for 28 and 23 patients, respectively. The median follow-up duration was 1434 (60 - 4062) days.
Fifty (98.0%) patients were successfully engrafted. Transplant-related mortality occurred in 8 (15.7%) patients. Acute graft-versus-host disease (aGVHD) occurred in 35 (68.6%) patients and 11 (21.6%) patients were grade II-IV, while chronic GVHD (cGVHD) did in 17 (37.8%) patients. Five (7.4%) patients relapsed. The 5-year probability of disease-free survival (DFS) was (79.2 +/- 6.4)%. There was no significant difference in 5-year DFS, death rate and treatment related syndromes between the two conditioning regimens (P > 0.05), and in 5-year DFS, relapse rate and death rate between two transplant choices (P > 0.05). However, the rate of relapse was lower in Bu/Cy group (P < 0.01) and the rate of cGVHD was higher in allo-PBSCT group (P < 0.05).
Allo-HSCT can cure a significant proportion of patients with CML-CP(1). There was no significant difference in DFS between the two different conditioning regimens and between the different transplant choices. Donor lymphocyte infusion is a therapeutic alternative for CML patients relapsed after transplantation.
评估人类白细胞抗原(HLA)全相合同胞异基因造血干细胞移植(allo-HSCT)治疗慢性髓性白血病(CML)慢性期(CP(1))患者的疗效。
51例CML-CP(1)患者接受了HLA全相合同胞allo-HSCT,预处理方案为全身照射(TBI)加环磷酰胺(Cy)或白消安(Bu)加Cy。分别对28例和23例患者进行了异基因外周血干细胞移植(PBSCT)和骨髓移植(BMT)。中位随访时间为1434(60 - 4062)天。
50例(98.0%)患者成功植入。8例(15.7%)患者发生移植相关死亡。35例(68.6%)患者发生急性移植物抗宿主病(aGVHD),11例(21.6%)患者为Ⅱ-Ⅳ级,17例(37.8%)患者发生慢性移植物抗宿主病(cGVHD)。5例(7.4%)患者复发。5年无病生存率(DFS)为(79.2±6.4)%。两种预处理方案之间的5年DFS、死亡率和治疗相关综合征无显著差异(P>0.05),两种移植选择之间的5年DFS、复发率和死亡率也无显著差异(P>0.05)。然而,Bu/Cy组的复发率较低(P<0.01),异基因PBSCT组的cGVHD发生率较高(P<0.05)。
allo-HSCT可治愈相当比例的CML-CP(1)患者。两种不同预处理方案之间以及不同移植选择之间的DFS无显著差异。供体淋巴细胞输注是移植后复发的CML患者的一种治疗选择。