儿童急性淋巴细胞白血病第二次完全缓解期异基因造血干细胞移植的结局:一项单中心研究
Outcome of allogeneic hematopoietic stem cell transplantation for childhood acute lymphoblastic leukemia in second complete remission: a single institution study.
作者信息
Lee Eun-Jung, Han Ji Yoon, Lee Jae Wook, Jang Pil-Sang, Chung Nack-Gyun, Jeong Dae-Chul, Cho Bin, Kim Hack-Ki
机构信息
Department of Pediatrics, The Catholic University of Korea, School of Medicine, Seoul, Korea.
出版信息
Korean J Pediatr. 2012 Mar;55(3):100-6. doi: 10.3345/kjp.2012.55.3.100. Epub 2012 Mar 16.
PURPOSE
The survival rate for childhood acute lymphoblastic leukemia (ALL) has improved significantly. However, overall prognosis for the 20 to 25% of patients who relapse is poor, and allogeneic hematopoietic stem cell transplantation (HSCT) offers the best chance for cure. In this study, we identified significant prognostic variables by analyzing the outcomes of allogeneic HSCT in ALL patients in second complete remission (CR).
METHODS
Fifty-three ALL patients (42 men, 79%) who received HSCT in second CR from August 1991 to February 2009 were included (26 sibling donor HSCTs, 49%; 42 bone marrow transplantations, 79%). Study endpoints included cumulative incidence of acute and chronic graft-versus-host disease (GVHD), relapse, 1-year transplant-related mortality (TRM), disease-free survival (DFS), and overall survival (OS).
RESULTS
Cumulative incidences of acute GVHD (grade 2 or above) and chronic GVHD were 45.3% and 28.5%, respectively. The estimated 5-year DFS and OS for the cohort was 45.2±6.8% and 48.3±7%, respectively. Only donor type, i.e., sibling versus unrelated, showed significant correlation with DFS in multivariate analysis (P=0.010). The rates of relapse and 1 year TRM were 28.9±6.4% and 26.4±6.1%, respectively, and unrelated donor HSCT (P=0.002) and HLA mismatch (P=0.022) were significantly correlated with increased TRM in univariate analysis.
CONCLUSION
In this single institution study spanning more than 17 years, sibling donor HSCT was the only factor predicting a favorable result in multivariate analysis, possibly due to increased TRM resulting from unrelated donor HSCT.
目的
儿童急性淋巴细胞白血病(ALL)的生存率已显著提高。然而,20%至25%复发患者的总体预后较差,异基因造血干细胞移植(HSCT)是治愈的最佳机会。在本研究中,我们通过分析处于第二次完全缓解(CR)的ALL患者异基因HSCT的结果,确定了显著的预后变量。
方法
纳入1991年8月至2009年2月期间在第二次CR时接受HSCT的53例ALL患者(42例男性,占79%)(26例同胞供体HSCT,占49%;42例骨髓移植,占79%)。研究终点包括急慢性移植物抗宿主病(GVHD)的累积发生率、复发率、1年移植相关死亡率(TRM)、无病生存率(DFS)和总生存率(OS)。
结果
急性GVHD(2级或以上)和慢性GVHD的累积发生率分别为45.3%和28.5%。该队列的估计5年DFS和OS分别为45.2±6.8%和48.3±7%。在多变量分析中,只有供体类型,即同胞与非血缘供体,与DFS显示出显著相关性(P=0.010)。复发率和1年TRM分别为28.9±6.4%和26.4±6.1%,在单变量分析中,非血缘供体HSCT(P=0.002)和HLA不匹配(P=0.022)与TRM增加显著相关。
结论
在这项跨越17年以上的单机构研究中,同胞供体HSCT是多变量分析中预测良好结果的唯一因素,这可能是由于非血缘供体HSCT导致TRM增加所致。