移植
临床试验
造血干细胞移植
骨髓增生异常综合症
医学
造血细胞
疾病
氟达拉滨
微小残留病
重症监护医学
内科学
肿瘤科
干细胞
白血病
化疗
造血
骨髓
生物
遗传学
环磷酰胺
作者
Alain Mina,Peter L. Greenberg,H. Joachim Deeg
出处
期刊:Blood
[American Society of Hematology]
日期:2024-02-02
卷期号:143 (14): 1344-1354
被引量:2
标识
DOI:10.1182/blood.2023023005
摘要
Abstract Allogeneic hematopoietic stem cell transplantation (HSCT) is the only potentially curative option for patients with high-risk myelodysplastic syndromes (MDS). Advances in conditioning regimens and supportive measures have reduced treatment-related mortality and increased the role of transplantation, leading to more patients undergoing HSCT. However, posttransplant relapse of MDS remains a leading cause of morbidity and mortality for this procedure, necessitating expert management and ongoing results analysis. In this article, we review treatment options and our institutional approaches to managing MDS relapse after HSCT, using illustrative clinical cases that exemplify different clinical manifestations and management of relapse. We address areas of controversy relating to conditioning regimen intensity, chemotherapeutic bridging, and donor selection. In addition, we discuss future directions for advancing the field, including (1) the need for prospective clinical trials separating MDS from acute myeloid leukemia and focusing on posttransplant relapse, as well as (2) the validation of measurable residual disease methodologies to guide timely interventions.
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