Allogeneic Transplant for CMML.

IF 3.3 3区 医学 Q2 HEMATOLOGY
Nico Gagelmann, Nihar Desai
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引用次数: 0

Abstract

Purpose of review: Chronic myelomonocytic leukemia (CMML) is a rare hematologic malignancy at the intersection of myelodysplastic (MDS) and myeloproliferative neoplasms, predominantly affecting older adults. Allogeneic hematopoietic cell transplantation (allo-HCT) remains the only curative option, yet its application is limited by the advanced age and comorbidities of most patients. Recent classification updates and refined prognostic tools, particularly molecularly integrated models like CPSS-Mol have enhanced patient stratification and informed transplant timing. The aim of this review is to highlight the evolving landscape of CMML management, with a focus on the role of allo-HCT.

Recent findings: Novel studies patients demonstrated that individualized transplant timing significantly improved life expectancy. Optimizing transplant outcomes hinges on several factors:managing pretransplant splenomegaly, choosing appropriate debulking strategies, selecting optimal donors, and tailoring conditioning regimens. New data favor treosulfan-based and thiotepa-busulfan regimens for their favorable toxicity and relapse profiles. Post-transplant, strategies like post-transplant cyclophosphamide (PTCy) for GVHD prophylaxis and emerging approaches to minimal residual disease (MRD) monitoring offer additional refinements in patient management. While no MRD studies are CMML-specific, extrapolation from MDS supports its role in relapse prediction. Innovative therapies, including hypomethylating agent combinations, venetoclax, targeted inhibitors, and immunotherapies are under active investigation, with potential to improve pre- and post-transplant outcomes. Advancements in molecular classification, dynamic prognostic tools, and therapeutic strategies are reshaping the CMML treatment paradigm. Personalized approaches that integrate genetic risk, patient fitness, and disease characteristics are enabling more effective transplant strategies, with the ultimate goal of extending survival and improving quality of life in this complex and historically difficult-to-treat malignancy.

同种异体移植治疗CMML。
综述目的:慢性髓细胞白血病(CMML)是一种罕见的血液系统恶性肿瘤,介于骨髓增生异常(MDS)和骨髓增生性肿瘤之间,主要影响老年人。同种异体造血细胞移植(allo-HCT)仍然是唯一的治疗选择,但其应用受到大多数患者高龄和合并症的限制。最近更新的分类和完善的预后工具,特别是分子集成模型,如CPSS-Mol,增强了患者分层和知情移植时机。这篇综述的目的是强调cml管理的发展前景,重点是allo-HCT的作用。最新发现:新的研究表明,个体化的移植时间可以显著提高患者的预期寿命。优化移植结果取决于几个因素:处理移植前脾肿大,选择适当的减容策略,选择最佳供体,以及定制调理方案。新的数据支持基于曲硫丹和硫特帕-布硫丹的方案,因为它们具有良好的毒性和复发特征。移植后,移植后环磷酰胺(PTCy)预防GVHD的策略和微小残留病(MRD)监测的新方法为患者管理提供了额外的改进。虽然没有MRD研究是cmml特异性的,但MDS的推断支持其在复发预测中的作用。创新疗法,包括低甲基化药物组合、venetoclax、靶向抑制剂和免疫疗法正在积极研究中,有可能改善移植前和移植后的预后。分子分类、动态预后工具和治疗策略的进步正在重塑CMML的治疗范式。整合遗传风险、患者适应性和疾病特征的个性化方法使更有效的移植策略成为可能,最终目标是延长这种复杂且历史上难以治疗的恶性肿瘤的生存期和提高生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.00
自引率
0.00%
发文量
28
审稿时长
>12 weeks
期刊介绍: his journal intends to provide clear, insightful, balanced contributions by international experts that review the most important, recently published clinical findings related to the diagnosis, treatment, management, and prevention of hematologic malignancy. We accomplish this aim by appointing international authorities to serve as Section Editors in key subject areas, such as leukemia, lymphoma, myeloma, and T-cell and other lymphoproliferative malignancies. Section Editors, in turn, select topics for which leading experts contribute comprehensive review articles that emphasize new developments and recently published papers of major importance, highlighted by annotated reference lists. An international Editorial Board reviews the annual table of contents, suggests articles of special interest to their country/region, and ensures that topics are current and include emerging research. Commentaries from well-known figures in the field are also provided.
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