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异基因造血干细胞移植治疗急性白血病后复发患儿的生存预后因素。

Prognostic factors for survival in children who relapsed after allogeneic hematopoietic stem cell transplantation for acute leukemia.

机构信息

Pediatric BMT Unit, Medstar Yıldız Hospital, Antalya, Turkey.

Pediatric BMT Unit, Medical Park Göztepe Hospital, Istanbul, Turkey.

出版信息

Pediatr Transplant. 2021 Aug;25(5):e13942. doi: 10.1111/petr.13942. Epub 2020 Dec 15.

Abstract

BACKGROUND

Post-transplant relapse has a dismal prognosis in children with acute leukemia undergoing allogeneic hematopoietic stem cell transplantation (allo-HSCT). Data on risk factors, treatment options, and outcomes are limited.

PROCEDURE

In this retrospective multicenter study in which a questionnaire was sent to all pediatric transplant centers reporting relapse after allo-HSCT for a cohort of 938 children with acute leukemia, we analyzed 255 children with relapse of acute leukemia after their first allo-HSCT.

RESULTS

The median interval from transplantation to relapse was 180 days, and the median follow-up from relapse to the last follow-up was 1844 days. The 3-year overall survival (OS) rate was 12.0%. The main cause of death was disease progression or subsequent relapse (82.6%). The majority of children received salvage treatment with curative intent without a second HSCT (67.8%), 22.0% of children underwent a second allo-HSCT, and 10.2% received palliative therapy. Isolated extramedullary relapse (hazard ratio (HR): 0.607, P = .011) and relapse earlier than 365 days post-transplantation (HR: 2.101, P < .001 for 0-180 days; HR: 1.522, P = .041 for 181-365 days) were found in multivariate analysis to be significant prognostic factors for outcome. The type of salvage therapy in chemosensitive relapse was identified as a significant prognostic factor for OS.

CONCLUSION

A salvage approach with curative intent may be considered for patients with post-transplant relapse, even if they relapse in the first year post-transplantation. For sustainable remission, a second allo-HSCT may be recommended for patients who achieve complete remission after reinduction treatment.

摘要

背景

异体造血干细胞移植(allo-HSCT)后移植后复发的急性白血病患儿预后较差。关于危险因素、治疗选择和结果的数据有限。

方法

本研究为回顾性多中心研究,我们向所有报告 allo-HSCT 后复发的儿科移植中心发送了一份问卷,对 938 例急性白血病患儿进行了队列研究,其中分析了 255 例首次 allo-HSCT 后发生急性白血病复发的患儿。

结果

从移植到复发的中位间隔时间为 180 天,从复发到最后随访的中位随访时间为 1844 天。3 年总生存率(OS)为 12.0%。死亡的主要原因是疾病进展或随后的复发(82.6%)。大多数患儿接受了根治性挽救治疗,而无需二次 HSCT(67.8%),22.0%的患儿接受了二次 allo-HSCT,10.2%的患儿接受了姑息治疗。孤立性髓外复发(危险比(HR):0.607,P=.011)和移植后 365 天内复发(0-180 天 HR:2.101,P<.001;181-365 天 HR:1.522,P=.041)是多变量分析中发现的与预后相关的显著预后因素。缓解治疗后在敏感缓解的患儿,挽救治疗的类型是 OS 的显著预后因素。

结论

即使在移植后 1 年内复发,也可考虑采用有治愈意向的挽救方法。对于那些在再诱导治疗后获得完全缓解的患者,建议进行第二次 allo-HSCT 以实现持续缓解。

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