阿扎胞苷联合venetoclax可缓解SDS中TP53突变的AML-MR:病例报告和文献综述。

IF 1.8 4区 医学 Q3 ONCOLOGY
Anti-Cancer Drugs Pub Date : 2024-07-01 Epub Date: 2024-03-14 DOI:10.1097/CAD.0000000000001594
Cuiping Ma, Haiyan Lang, Yuhan Chen, Lu Yang, Chong Wang, Lizhen Han, Xinyi Chen, Wei Ma
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引用次数: 0

摘要

舒瓦赫曼-钻石综合征(SDS)是一种常染色体隐性遗传病,易转化为骨髓增生异常综合征(MDS)和急性髓性白血病(AML)。TP53 基因突变是 SDS 向 MDS/AML 转化以及 MDS 向 AML 演变的驱动因素。异基因造血干细胞移植(Allo-HSCT)是唯一可治愈的方法,然而,如何在疗效与治疗相关毒性和死亡率的高风险之间取得平衡,在移植前实现暂时性疾病控制,为移植赢得时间和机会,仍是一项挑战。目前,移植前桥接疗法已成为重要的选择之一,它能提高疗效、减轻肿瘤负荷、减少治疗相关毒性。在此,我们报道了阿扎胞苷联合venetoclax作为移植前桥接疗法用于一例由SDS发展而来的TP53突变AML-MR病例。该患者在完全缓解且未完全康复的情况下接受了异基因造血干细胞移植(Allo-HSCT)。我们希望通过本病例的介绍,为深入研究和临床治疗提供一些证据和启示。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Azacitidine combined with venetoclax alleviates AML-MR with TP53 mutation in SDS: a case report and literature review.

Shwachman-Diamond syndrome (SDS) is an autosomal recessive genetic disease, which is prone to transform into myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML). TP53 mutation is a driving factor involved in the transformation of SDS into MDS/AML, and in the evolution of MDS to AML. Allogeneic hematopoietic stem cell transplantation (Allo-HSCT) is the only curable approach, however, challenge remains regarding the balance between efficacy and the high risk from treatment-related toxicity and mortality to achieve temporary disease control before transplantation to gain time and opportunities for transplantation. At present, pre-transplant bridging therapy has emerged as one of the important options with improved efficacy, reduced tumor burden, and less treatment-related toxicity. Here we reported azacitidine combined with venetoclax was used as pre-transplant bridging regimen in a TP53-mutant AML-MR case developed from SDS. He achieved complete remission with incomplete recovery and proceeded to Allo-HSCT. We hope to provide some evidence and insight for in-depth research and clinical treatment by presenting this case.

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来源期刊
Anti-Cancer Drugs
Anti-Cancer Drugs 医学-药学
CiteScore
3.80
自引率
0.00%
发文量
244
审稿时长
3 months
期刊介绍: Anti-Cancer Drugs reports both clinical and experimental results related to anti-cancer drugs, and welcomes contributions on anti-cancer drug design, drug delivery, pharmacology, hormonal and biological modalities and chemotherapy evaluation. An internationally refereed journal devoted to the fast publication of innovative investigations on therapeutic agents against cancer, Anti-Cancer Drugs aims to stimulate and report research on both toxic and non-toxic anti-cancer agents. Consequently, the scope on the journal will cover both conventional cytotoxic chemotherapy and hormonal or biological response modalities such as interleukins and immunotherapy. Submitted articles undergo a preliminary review by the editor. Some articles may be returned to authors without further consideration. Those being considered for publication will undergo further assessment and peer-review by the editors and those invited to do so from a reviewer pool.
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