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Retrospective Analysis of the Treatment Outcome in Myeloid Leukemia of Down Syndrome in Polish Pediatric Leukemia and Lymphoma Study Group From 2005 to 2019

机译:2005至2019年波兰小儿白血病唐氏综合征骨髓白血病治疗结果的回顾性分析

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Background: Children with Down syndrome (DS) have increased risk of myeloid leukemia (ML), but specific treatment protocols ensure excellent outcome. This study was a retrospective analysis of the treatment results and genetic characteristics of ML of DS (ML-DS) in Poland from 2005 to 2019. Methods: All 54 patients with ML-DS registered in the Polish Pediatric Leukemia and Lymphoma Study Group in analyzed period were enrolled to the study. There were 34 children treated with Acute Myeloid Leukemia–Berlin-Frankfurt-Munster 2004 Interim Protocol (group I) and 20 patients treated with ML-DS 2006 Protocol (group II). In the first protocol, there was reduction of the antracyclines doses and intrathecal treatment for ML-DS compared to non-DS patients. In the second protocol, further reduction of the treatment was introduced (omission of etoposide in the last cycle, no maintenance therapy). Results: Probabilities of 5-year overall survival (OS), event-free survival (EFS), and relapse-free survival in the whole analyzed group were 0.85 ± 0.05, 0.83 ± 0.05, and 0.97 ± 0.03, respectively. No significant differences were found between two protocols in the terms of OS and EFS (0.79 ± 0.07 vs. 0.95 ± 0.05, p = 0.14, and 0.76 ± 0.07 vs. 0.95 ± 0.05, p = 0.12, respectively). All deaths were caused by the treatment-related toxicities. Reduction of the treatment-related mortality was noticed (20% in group I and 5% in group II). The only one relapse in the whole cohort occurred in the patient from group I, older than 4 years, without GATA1 gene mutation. He was treated successfully with IdaFLA cycle followed by hematopoietic stem cell transplantation from matched sibling donor. No significant prognostic factor was found in the study group probably due to low number of patients in the subgroups. Conclusions: The study confirms that the reduced intensity protocols are very effective in ML-DS patients. The only cause of deaths was toxicities; however, systematic decrease of the treatment-related mortality was noticed.
机译:背景:唐氏综合症(DS)的儿童增加了骨髓白血病(ML)的风险,但具体的治疗方案确保了出色的结果。该研究是从2005年到2019年开始对波兰的DS(ML-DS)Ml(ML-DS)的治疗结果和遗传特征的回顾性分析。方法:在波兰小儿白血病和淋巴瘤研究组中注册的所有54例ML-DS患者分析期限已注册研究。有34名儿童治疗急性髓性白血病 - 柏林 - 法兰克福 - Munster 2004年临时协议(I型)和20名患有ML-DS 2006议定书的患者(II组)。在第一方案中,与非DS患者相比,对ML-DS的ML-DS进行了减少的亚锡管剂量和鞘内治疗。在第二方案中,引入了进一步减少治疗(在最后一个循环中遗漏依托泊苷,没有维持治疗)。结果:整个分析组的5年总存活(OS),无事项存活率(EFS)和无复发存活的概率分别为0.85±0.05,0.83±0.05和0.97±0.03。在OS和EF的两种方案之间没有发现显着差异(0.79±0.07与0.95±0.05,P = 0.14和0.76±0.07和0.95±0.05,P = 0.12)。所有死亡均由治疗有关的毒性引起。将注意到治疗相关的死亡率(II组中的20%和5%)。整个队列中唯一的复发,患者患者来自4年的患者,没有GATA1基因突变。他用idafla循环成功治疗,然后由匹配的兄弟供体中的造血干细胞移植。在研究组中没有发现显着的预后因子可能是由于亚组中患者数量的患者较少。结论:该研究证实,降低的强度方案在ML-DS患者中非常有效。死亡的唯一原因是毒性;然而,注意到治疗相关死亡率的系统性降低。

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