Allogeneic hematopoietic stem cell transplantation from matched related donors for acute myeloid leukemia.

IF 1.5 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL
Balazs Galffy, Ladislav Sopko, Jozef Lukas, Michaela Martisova, Barbora Ziakova, Peter Rohon, Silvia Cingelova, Martin Mistrik, Eva Bojtarova, Angelika Batorova
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引用次数: 0

Abstract

Introduction: In patients with acute myeloid leukemia (AML), allogeneic hematopoietic stem cell transplantation (HSCT) remains the priority treatment option as the most effective prevention of relapse. When an HLA-matched sibling is available, these transplants are preferred.

Objectives: We stratificated patients according to risk, disease state (an active disease, the 1st or 2nd complete remission ‒ CR1, CR2, which was achieved after the 1st or 2nd induction) and type of graft (from brother or sister). Finally, the overall survival (OS) of patients in individual groups was evaluated.

Material and methods: The retrospective single-center study included 104 transplantations in 97 adult patients with AML who underwent HSCT from matched sibling donor in a period of 10 years between January 2011 and December 2020.

Results: 54 patients (55.7%) were alive as of the January 1, 2022. The median OS of the entire group, as well as the cohort with favorable (5y-OS 75.0%) and intermediate prognosis risk (5y‒OS 78.5%) was not reached. We found that patients, who required second induction therapy to achieve CR, had poorer OS after allogeneic HSCT, median 20.7 months (95% CI, 6.5-35.5) than those who achieved CR after first induction, median not reached (95% CI, 63.5‒63.5, p=0.0048). Statistically significant effect on OS shows transplantation in CR2 (HR 6.76, CI 95% 2.19‒20.80, p=0.0009), In addition, this parameter influenced OS more than achieving CR up to the 2nd induction course (HR 2.44, CI 95% 1.17‒5.11; p=0.0180) or entry to transplantation without CR (HR 2.81, CI 95% 1.09‒7.26; p=0.0326).

Conclusion: The results presented in the work show the high efficiency of HSCT in each risk group. The number of induction therapies required to achieve CR is a good prognostic factor. The gender of a sibling has no impact on OS (Tab. 11, Fig. 7, Ref. 18). Text in PDF www.elis.sk Keywords: acute myeloid leukemia, allogeneic hematopoietic stem cell transplantation, overall survival, remission status, donor tender.

急性髓性白血病的配型亲属异体造血干细胞移植。
简介在急性髓性白血病(AML)患者中,异基因造血干细胞移植(HSCT)仍是最有效的预防复发的优先选择。如果有HLA匹配的兄弟姐妹,这些移植是首选:我们根据风险、疾病状态(活动性疾病、第一次或第二次完全缓解--CR1、CR2,在第一次或第二次诱导后达到)和移植类型(来自兄弟或姐妹)对患者进行了分层。最后,对各组患者的总生存期(OS)进行了评估:这项回顾性单中心研究纳入了 2011 年 1 月至 2020 年 12 月的 10 年间,97 名接受匹配同胞供者造血干细胞移植的急性髓细胞性白血病成年患者的 104 例移植:截至2022年1月1日,54名患者(55.7%)存活。整组患者以及预后良好(5 年生存率为 75.0%)和预后中等风险(5 年生存率为 78.5%)患者的中位生存率均未达到预期。我们发现,需要第二次诱导治疗才能达到 CR 的患者,其异体造血干细胞移植后的 OS 较差,中位数为 20.7 个月(95% CI,6.5-35.5),低于第一次诱导治疗后达到 CR 的患者,中位数未达到(95% CI,63.5-63.5,P=0.0048)。此外,该参数对OS的影响大于在第2个诱导疗程前达到CR(HR 2.44,CI 95% 1.17-5.11;P=0.0180)或未达到CR即进行移植(HR 2.81,CI 95% 1.09-7.26;P=0.0326):本文的研究结果表明,造血干细胞移植在各个风险组别中都具有很高的效率。达到 CR 所需的诱导治疗次数是一个很好的预后因素。同胞的性别对OS没有影响(表11,图7,参考文献18)。PDF 格式的文本 www.elis.sk 关键词:急性髓性白血病、异基因造血干细胞移植、总生存期、缓解状态、供体柔嫩。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.60
自引率
0.00%
发文量
185
审稿时长
3-8 weeks
期刊介绍: The international biomedical journal - Bratislava Medical Journal – Bratislavske lekarske listy (Bratisl Lek Listy/Bratisl Med J) publishes peer-reviewed articles on all aspects of biomedical sciences, including experimental investigations with clear clinical relevance, original clinical studies and review articles.
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