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异基因造血干细胞移植后复发的急性髓系白血病或骨髓增生异常综合征的阿扎胞苷治疗,多中心 PALG 分析。

Azacitidine for relapse of acute myeloid leukemia or myelodysplastic syndrome after allogeneic hematopoietic stem cell transplantation, multicenter PALG analysis.

机构信息

Department of Hematology, Transplantation and Internal Medicine, Medical University of Warsaw, Warsaw, Poland.

Faculty of Mathematics and Information Science, Warsaw University of Technology, Warsaw, Poland.

出版信息

Eur J Haematol. 2021 Jul;107(1):129-136. doi: 10.1111/ejh.13628. Epub 2021 Apr 4.

Abstract

OBJECTIVES

Relapse of myelodysplastic syndromes (MDS) or acute myeloid leukemia (AML) after allogeneic hematopoietic stem cell transplantation (allo-HSCT) belongs to the major causes of treatment failure.

METHODS

Retrospective multicenter analysis of patients diagnosed with AML or MDS who had hematological relapse after allo-HSCT and were treated with azacitidine for this indication.

RESULTS

Twenty-three patients receiving azacitidine as the first treatment of relapse (Group_1) and 8 patients receiving azacitidine after other treatment of relapse (Group_2) were included. There were 68% males, median age at initiation of azacitidine was 53 years (15-66). Median time to relapse was 3.5 months and 6.3 months in Group_1 and Group_2, respectively; median time from relapse to azacitidine 0.2 and 2.3 months. Azacitidine 75 mg/m , days 1-7, was administered in 78% and 75% of patients in Group_1 and Group_2, concomitant DLI in 48% and 50%. With median follow-up of 4.7 and 13.6 months, the median overall survival was 5.9 and 9.5 months. 17% and 37.5% patients proceeded to salvage allo-HSCT, with median OS of 11.6 months and not reached respectively.

CONCLUSIONS

Azacitidine treatment for hematological relapse is associated with poor outcome; nevertheless, a proportion of patients may benefit from it, including patients receiving subsequent salvage allo-HSCT.

摘要

目的

异基因造血干细胞移植(allo-HSCT)后骨髓增生异常综合征(MDS)或急性髓系白血病(AML)的复发属于治疗失败的主要原因之一。

方法

回顾性分析了诊断为 AML 或 MDS 的患者,这些患者在 allo-HSCT 后发生血液学复发,并接受阿扎胞苷治疗。

结果

共纳入 23 例患者接受阿扎胞苷作为复发的一线治疗(组 1),8 例患者在其他治疗方案失败后接受阿扎胞苷治疗(组 2)。男性占 68%,阿扎胞苷起始年龄的中位数为 53 岁(15-66 岁)。组 1 和组 2 的中位复发时间分别为 3.5 个月和 6.3 个月;从复发到阿扎胞苷的中位时间分别为 0.2 个月和 2.3 个月。组 1 和组 2 中分别有 78%和 75%的患者接受了 75mg/m 的阿扎胞苷治疗,第 1-7 天;48%和 50%的患者接受了同时的供者淋巴细胞输注(DLI)。在中位随访 4.7 个月和 13.6 个月时,中位总生存期分别为 5.9 个月和 9.5 个月。17%和 37.5%的患者接受了挽救性 allo-HSCT,中位 OS 分别为 11.6 个月和未达到。

结论

阿扎胞苷治疗血液学复发的疗效不佳;然而,仍有一部分患者可能从中获益,包括接受后续挽救性 allo-HSCT 的患者。

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