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针对具有不良遗传学特征的急性髓系白血病的精准医学方法。

Precision Medicine Approaches in Acute Myeloid Leukemia with Adverse Genetics.

作者信息

Santoro Nicole, Salutari Prassede, Di Ianni Mauro, Marra Andrea

机构信息

Hematology Unit, Department of Hematology and Oncology, Ospedale Civile "Santo Spirito", 65122 Pescara, Italy.

Department of Medicine and Science of Aging, "G.D'Annunzio" University of Chieti-Pescara, 66100 Chieti, Italy.

出版信息

Int J Mol Sci. 2024 Apr 11;25(8):4259. doi: 10.3390/ijms25084259.

Abstract

The treatment of acute myeloid leukemia (AML) with adverse genetics remains unsatisfactory, with very low response rates to standard chemotherapy and shorter durations of remission commonly observed in these patients. The complex biology of AML with adverse genetics is continuously evolving. Herein, we discuss recent advances in the field focusing on the contribution of molecular drivers of leukemia biogenesis and evolution and on the alterations of the immune system that can be exploited with immune-based therapeutic strategies. We focus on the biological rationales for combining targeted therapy and immunotherapy, which are currently being investigated in ongoing trials, and could hopefully ameliorate the poor outcomes of patients affected by AML with adverse genetics.

摘要

对具有不良遗传学特征的急性髓系白血病(AML)的治疗仍不尽人意,这些患者对标准化疗的反应率非常低,且缓解期通常较短。具有不良遗传学特征的AML复杂生物学特性在不断演变。在此,我们讨论该领域的最新进展,重点关注白血病发生和演变的分子驱动因素的作用以及可通过基于免疫的治疗策略加以利用的免疫系统改变。我们关注联合靶向治疗和免疫治疗的生物学原理,目前正在进行的试验中对其进行研究,有望改善受具有不良遗传学特征的AML影响患者的不良预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf2b/11050344/2c4aaa22f331/ijms-25-04259-g001.jpg

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