[Venetoclax联合地西他滨、改良HA方案和DLI治疗异基因造血干细胞移植后复发的小儿急性髓细胞白血病/MDS的有效性和安全性]。

F Zhang, H F Wang, G H Hu, P Suo, L Bai, Y Wang, X H Zhang, X J Huang, Y F Cheng
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引用次数: 0

摘要

目的研究Venetoclax联合地西他滨、阿糖胞苷和同型异构化干细胞移植(HSCT)方案和供体淋巴细胞输注(DLI)对异基因造血干细胞移植(HSCT)后小儿急性髓性白血病(AML)/骨髓增生异常综合征(MDS)预防和挽救治疗的有效性和安全性。方法:2021年1月1日至2023年6月1日,北京大学血液病研究所共招募了29例造血干细胞移植后复发的小儿/最小残留病阳性AML患者。他们接受上述联合方案治疗,并在化疗结束24-48小时后给予DLI,定期评估治疗反应和不良反应。结果血液学复发组的总反应率(ORR)为75.8%,CR率为88.9%(8/9),MRD阳性组的MRD阴性率为61.1%(11/18)。粒细胞减少症、贫血和血小板减少症三级以上的发生率分别为100%、82.7%和100%。粒细胞缺乏期的中位时间为 15 天。DLI 后,11.1% 的患者发生了Ⅲ-Ⅳ级急性移植物抗宿主疾病(aGVHD),7.4% 的患者发生了中度或重度 cGVHD。MNC计数低于10×10(8)/kg是导致ORR的唯一风险因素,而且复发发生在100天内。中位随访期为406天,1年生存率为65%,无反应组的1年生存率为57%(P=0.164),而有总体反应组的1年生存率为71%。结论在造血干细胞移植复发后的小儿急性髓细胞白血病挽救治疗中,基于DAC、VEN和改良HA方案的联合方案显示出较高的反应率。不过,应在病情缓解后立即进行移植桥接,以提高存活率。
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[Efficacy and safety of venetoclax combined with decitabine, modified HA regimen and DLI in the treatment of relapsed pediatric AML/MDS after allogeneic hematopoietic stem cell transplantation].

Objective: To investigate the efficacy and safety of venetoclax combined with the decitabine, cytarabine, and homoharringtonine (HHT) regimen and donor lymphocyte infusion (DLI) for the preventive and salvage therapy of pediatric acute myeloid leukemia (AML) /myelodysplastic syndrome (MDS) after allogeneic hematopoietic stem cell transplantation (HSCT) . Methods: A total of 29 relapsed pediatric/minimal residual disease-positive AML after HSCT were recruited at the Peking University Institute of Hematology from January 1, 2021, to June 1, 2023. They were treated with the above combination regimen and administered with DLI after 24-48 hours at the end of chemotherapy, and the treatment response and adverse reactions were regularly assessed. Results: The overall response rate (ORR) was 75.8%, CR rate was 88.9% (8/9) in the hematologic relapse group, and MRD negativity rate was 61.1% (11/18) in the MRD-positive group. The incidence of agranulocytosis, anemia, and thrombocytopenia with a classification above grade 3 were 100%, 82.7%, and 100%, respectively. The median time of the granulocyte deficiency period was 15 days. Acute graft-versus-host diseases (aGVHD) with a classification of grades Ⅲ-Ⅳ occurred in 11.1% of the patients after DLI, while moderate or severe cGVHD occurred in 7.4% of the patients. The single risk factor for ORR was MNC counts of less than 10×10(8)/kg, and the relapse occurred within 100 days. At a median follow-up of 406 days, the 1-year OS was 65%, and the 1-year OS was 57% in the group with no reaction (P=0.164) compared with 71% in the group who had an overall reaction. Conclusion: The combined regimen based on the DAC, VEN, and modified HA regimen showed a high response rate in the salvage therapy for pediatric AML after the relapse of HSCT. However, bridging to transplantation should be performed immediately after remission to result in a long survival rate.

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