Hematopoieitic Cell Transplant and Cell Therapy Program, Massachusetts General Hospital, Boston, Massachusetts.
Hematopoietic Stem Cell Transplantation and Cellular Therapy Program, Division of Hematology/Oncology, Department of Medicine, University of California Irvine, Orange, California.
Transplant Cell Ther. 2023 Feb;29(2):71-81. doi: 10.1016/j.jtct.2022.11.014. Epub 2022 Nov 25.
The sole curative therapy for myelodysplastic syndrome (MDS) is allogeneic hematopoietic cell transplantation (HCT). Here this therapeutic modality is reviewed and critically evaluated in the context of the evidence. Specific criteria were used for searching the published literature and for grading the quality and strength of the evidence and the strength of the recommendations. A panel of MDS experts comprising transplantation and nontransplantation physicians developed consensus treatment recommendations. This review summarizes the standard MDS indications for HCT and addresses areas of controversy. Recent prospective trials have confirmed that allogeneic HCT confers survival benefits in patients with advanced or high-risk MDS compared with nontransplantation approaches, and the use of HCT is increasing in older patients with good performance status. However, patients with high-risk cytogenetic or molecular mutations remain at high risk for relapse. It is unknown whether administration of novel therapies before or after transplantation may decrease the risk of disease relapse in selected populations. Ongoing and future studies will investigate revised approaches to disease risk stratification, patient selection, and post-transplantation approaches to optimize allogeneic HCT outcomes for patients with MDS.
骨髓增生异常综合征 (MDS) 的唯一根治性治疗方法是异基因造血细胞移植 (HCT)。本文结合相关证据对此治疗方法进行了回顾和评价。通过特定的标准检索了已发表的文献,并对证据的质量和强度以及推荐的强度进行了分级。一个由移植和非移植医生组成的 MDS 专家小组制定了共识治疗建议。本综述总结了 MDS 进行 HCT 的标准适应证,并讨论了存在争议的领域。最近的前瞻性试验证实,与非移植方法相比,异基因 HCT 可使晚期或高危 MDS 患者获得生存获益,且在体能状态良好的老年患者中,HCT 的应用正在增加。然而,具有高危细胞遗传学或分子突变的患者仍存在高复发风险。尚不清楚在特定人群中,在移植前或移植后应用新型疗法是否可以降低疾病复发的风险。正在进行和未来的研究将探讨疾病风险分层、患者选择以及移植后处理等方面的修订方法,以优化 MDS 患者的异基因 HCT 结局。