基于 Venetoclax 的急性髓性白血病治疗:异基因造血干细胞移植道路上的意外收获?

IF 2.2 4区 医学 Q3 HEMATOLOGY
Leukemia & Lymphoma Pub Date : 2024-12-01 Epub Date: 2024-07-23 DOI:10.1080/10428194.2024.2381649
Francesco Tarantini, Cosimo Cumbo, Luisa Anelli, Antonella Zagaria, Nicoletta Coccaro, Giuseppina Tota, Angela Minervini, Crescenzio Francesco Minervini, Elisa Parciante, Maria Rosa Conserva, Immacolata Redavid, Giorgina Specchia, Pellegrino Musto, Francesco Albano
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引用次数: 0

摘要

尽管新药已获批准,组学数据已被纳入,机器学习也已融入诊断和治疗过程,但急性髓性白血病(AML)的预后仍然不容乐观。大多数患者的治愈途径仍然是成功进行异基因造血干细胞移植(HSCT)。然而,只有符合条件的患者才有机会接受造血干细胞移植。此外,造血干细胞移植后的疗效还受到急性髓细胞性白血病异质性和患者相关因素的影响。以venetoclax(VEN)为基础的联合用药已成为治疗老年或体质不佳急性髓细胞白血病患者的标准疗法,再加上其特殊的管理模式,促使研究人员开始评估这种方法在进行造血干细胞移植的患者中的可行性。我们回顾了现有的证据,以权衡这种新治疗策略的优势和缺陷。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Venetoclax-based treatment in acute myeloid leukemia: an unexpected bonus on the path to allogeneic hematopoietic stem cell transplant?

Despite the approval of new drugs, the inclusion of -omics-derived data and the integration of machine learning in both the diagnostic and therapeutic process, the prognosis of acute myeloid leukemia (AML) remains dismal. The curative path is still aimed at achieving a successful allogeneic hematopoietic stem cell transplant (HSCT) in most patients. Nevertheless, access to this procedure is limited to eligible patients. Moreover, post-HSCT outcomes are influenced by AML heterogeneity and patient-related factors. The rise of venetoclax (VEN)-based combinations as standard of care in the treatment of older or unfit AML patients, together with their peculiar management profile, has led researchers to evaluate the feasibility of this approach in patients proceeding toward HSCT. We reviewed the available evidence to weigh up the advantages and pitfalls of this new therapeutic strategy.

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来源期刊
Leukemia & Lymphoma
Leukemia & Lymphoma 医学-血液学
CiteScore
4.10
自引率
3.80%
发文量
384
审稿时长
1.8 months
期刊介绍: Leukemia & Lymphoma in its fourth decade continues to provide an international forum for publication of high quality clinical, translational, and basic science research, and original observations relating to all aspects of hematological malignancies. The scope ranges from clinical and clinico-pathological investigations to fundamental research in disease biology, mechanisms of action of novel agents, development of combination chemotherapy, pharmacology and pharmacogenomics as well as ethics and epidemiology. Submissions of unique clinical observations or confirmatory studies are considered and published as Letters to the Editor
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