Pediatric BMT Unit, Medstar Yıldız Hospital, Antalya, Turkey.
Pediatric BMT Unit, Medical Park Göztepe Hospital, Istanbul, Turkey.
Pediatr Transplant. 2021 Aug;25(5):e13942. doi: 10.1111/petr.13942. Epub 2020 Dec 15.
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.
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.
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.
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.
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。
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。
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。
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。