Prognostic impact of total body irradiation dose in pediatric acute lymphoblastic leukemia patients treated with allogeneic hematopoietic stem cell transplantation in second complete remission.

IF 2.3 Q2 HEMATOLOGY Blood Research Pub Date : 2022-12-31 DOI:10.5045/br.2022.2022174
Wonjin Jang, Suejung Jo, Jae Won Yoo, Seongkoo Kim, Jae Wook Lee, Pil-Sang Jang, Nack-Gyun Chung, Bin Cho
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Abstract

Background: Allogeneic HSCT may improve survival in pediatric ALL patients who relapse. In this study, we analyzed the outcome and prognostic factors of 62 ALL patients (35 male, 56.5%) who received allogeneic HSCT in second complete remission (CR) at our institution between April 1st 2009 and December 31st 2019.

Methods: The median time from diagnosis to relapse was 35.1 months (range, 6.0‒113.6 mo). Fifty-three patients (85.5%) experienced bone marrow relapse only. The number of patients who received transplant according to each donor type was as follows: HLA matched family donor 17 (27.4%), matched unrelated donor (UD) 22 (35.5%), mismatched donor 23 (37.1%). All patients received HSCT with a myeloablative conditioning, 58 patients (93.5%) with the incorporation of TBI [31 patients 12 Gray (Gy), 24 patients 13.2 Gy, 3 patients 8 Gy].

Results: The 5-year event-free survival (EFS), and overall survival of the study group was 41.3±6.3% (26/62), and 42.3±6.6% (27/62), respectively. The cumulative incidence of relapse and transplant-related mortality was 57.1±6.4% and 1.6±1.6%, respectively. Infant ALL, shorter time from diagnosis to relapse, and TBI dose of 12 Gy, rather than 13.2 Gy, resulted in significantly worse EFS. In multivariate analysis, infant ALL and TBI dose of 12 Gy during conditioning predicted significantly lower EFS.

Conclusion: In our study group, treatment with a higher dose of TBI during conditioning resulted in better EFS for ALL patients who underwent HSCT in second CR. Further study is needed to determine potential long-term complications associated with a higher TBI dose.

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全身照射剂量对小儿急性淋巴细胞白血病异基因造血干细胞移植第二次完全缓解患者预后的影响。
背景:同种异体造血干细胞移植可能提高复发的儿科ALL患者的生存率。在这项研究中,我们分析了2009年4月1日至2019年12月31日在我们机构接受第二次完全缓解(CR)的62例ALL患者(35例男性,56.5%)的结局和预后因素。方法:从诊断到复发的中位时间为35.1个月(范围:6.0-113.6个月)。53例(85.5%)仅发生骨髓复发。按供体类型进行移植的患者数为:HLA匹配家族供体17例(27.4%),匹配非亲属供体22例(35.5%),错配供体23例(37.1%)。所有患者均接受骨髓清除条件下的HSCT, 58例(93.5%)合并TBI[31例12 Gy, 24例13.2 Gy, 3例8 Gy]。结果:研究组的5年无事件生存率(EFS)和总生存率分别为41.3±6.3%(26/62)和42.3±6.6%(27/62)。累计复发率和移植相关死亡率分别为57.1±6.4%和1.6±1.6%。婴儿ALL,从诊断到复发的时间较短,TBI剂量为12 Gy而不是13.2 Gy,导致EFS明显恶化。在多变量分析中,调节期间婴儿ALL和TBI剂量为12 Gy预测显著降低的EFS。结论:在我们的研究组中,在第二次CR中接受HSCT的ALL患者,在适应症期间接受更高剂量的TBI治疗可以获得更好的EFS,需要进一步的研究来确定高剂量TBI相关的潜在长期并发症。
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来源期刊
Blood Research
Blood Research HEMATOLOGY-
CiteScore
3.70
自引率
0.00%
发文量
64
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