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含地西他滨预处理方案的异基因造血干细胞移植治疗TP53突变型骨髓增生异常综合征:一例病例报告

Allogeneic haematopoietic stem cell transplantation with decitabine-containing preconditioning regimen in TP53-mutant myelodysplastic syndromes: A case study.

作者信息

Wang Yuxin, Sun Yao, Xie Jing, Hu Jiangwei, Liu Na, Chen Jianlin, Li Botao, Lan Sanchun, Niu Jingwen, Wang Lei, Qiao Zhuoqing, Zhang Yu, Ren Jing, Zhang Bin, Qian Liren, Tan Yehui, Dou Liping, Li Yuhang, Hu Liangding

机构信息

Senior Department of Hematology, The Fifth Medical Centre of Chinese People's Liberation Army General Hospital, Beijing, China.

Department of Hematology, The First Hospital of Jilin University, Changchun, China.

出版信息

Front Oncol. 2022 Jul 18;12:928324. doi: 10.3389/fonc.2022.928324. eCollection 2022.

Abstract

Myelodysplastic syndrome (MDS) with TP53 mutations has a poor prognosis after transplantation, and novel therapeutic means are urgently needed. Decitabine (Dec) monotherapy has demonstrated improved overall response rates in MDS and acute myeloid leukaemia, although these responses were not durable. This study aimed to preliminary evaluate the efficacy of a Dec-containing allogeneic haematopoietic stem cell transplantation (allo-HSCT) preconditioning regimen in TP53-mutant MDS. Nine patients with TP53-mutant myelodysplastic syndromes received the decitabine-containing preconditioning regimen and subsequent myeloablative allo-HCT between April 2013 and September 2021 in different centres. At a median follow-up of 42 months (range, 5 to 61 months), the overall survival (OS) was 89% (8/9), progression-free survival (PFS) was 89% (8/9), and relapse incidence was 11.1%. The incidence of severe acute (grade III-IV) graft-versus-host disease (GVHD) was 22.2% (2/9) and that of chronic moderate-to-severe GVHD was 11.1% (1/9). The 1-year GVHD-free/relapse-free survival (GRFS) was 56% (5/9). In conclusion, we found real-world clinical data that supports the use of a Dec-containing preconditioning regimen before allo-HSCT for possible improved outcomes in TP53-mutant MDS patients; there is therefore an urgent call for an in-depth exploration of the involved mechanism to confirm these preliminary findings.

摘要

伴有TP53突变的骨髓增生异常综合征(MDS)患者移植后预后较差,急需新的治疗方法。地西他滨(Dec)单药治疗已显示出可提高MDS和急性髓系白血病的总体缓解率,尽管这些缓解并不持久。本研究旨在初步评估含Dec的异基因造血干细胞移植(allo-HSCT)预处理方案对TP53突变型MDS的疗效。2013年4月至2021年9月期间,9例TP53突变型骨髓增生异常综合征患者在不同中心接受了含地西他滨的预处理方案及随后的清髓性异基因造血细胞移植。中位随访42个月(范围5至61个月)时,总生存率(OS)为89%(8/9),无进展生存率(PFS)为89%(8/9),复发率为11.1%。重度急性(III-IV级)移植物抗宿主病(GVHD)的发生率为22.2%(2/9),慢性中重度GVHD的发生率为11.1%(1/9)。1年无GVHD/无复发生存率(GRFS)为56%(5/9)。总之,我们发现了真实世界的临床数据,支持在allo-HSCT前使用含Dec的预处理方案,可能改善TP53突变型MDS患者的预后;因此,迫切需要深入探索相关机制以证实这些初步发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4202/9339648/e09d78bde4ee/fonc-12-928324-g001.jpg

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