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治疗儿童白血病的新型药物:最新进展

Novel agents for the treatment of childhood leukemia: an update.

作者信息

Eryılmaz Ertugrul, Canpolat Cengiz

机构信息

Department of Pediatrics, Division of Pediatric Hematology and Oncology, Acibadem Maslak Hospital.

Department of Pediatric Hematology and Oncology, Acibadem Kozyatagi Hospital, Acıbadem University School of Medicine, Istanbul, Turkey.

出版信息

Onco Targets Ther. 2017 Jul 4;10:3299-3306. doi: 10.2147/OTT.S126368. eCollection 2017.

DOI:10.2147/OTT.S126368
PMID:28740405
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5505617/
Abstract

Achieving lower morbidity and higher survival rates in the treatment of childhood leukemia has been a paradigm of success in modern oncology. However, serious long-term health complications occur in very large populations of childhood leukemia survivors, in the case of both acute lymphoid leukemia and acute myeloid leukemia (AML). Additionally, 15% of acute lymphoid leukemia patients have treatment failures, and rates are even higher in childhood AML. In the last few decades, as a result of well-tested experiments that statistically analyzed treatment cohorts, new agents have emerged as alternatives or supplements to established treatments, in which high survival and/or less morbidity were observed. This review provides an overview of better practice in the treatment of childhood leukemia.

摘要

在儿童白血病治疗中实现更低的发病率和更高的生存率,已成为现代肿瘤学成功的典范。然而,在大量儿童白血病幸存者中,无论是急性淋巴细胞白血病还是急性髓系白血病(AML),都会出现严重的长期健康并发症。此外,15%的急性淋巴细胞白血病患者治疗失败,儿童AML的治疗失败率更高。在过去几十年里,经过充分测试并对治疗队列进行统计分析的实验,催生了新的药物,作为既定治疗方法的替代或补充,这些新药物显示出高生存率和/或更低的发病率。本综述概述了儿童白血病治疗的更佳实践。

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本文引用的文献

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Small molecule activation of NOTCH signaling inhibits acute myeloid leukemia.小分子激活 NOTCH 信号通路抑制急性髓系白血病。
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Making Better Chimeric Antigen Receptors for Adoptive T-cell Therapy.为过继性T细胞疗法制备更优的嵌合抗原受体
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Chimeric Antigen Receptors Modified T-Cells for Cancer Therapy.用于癌症治疗的嵌合抗原受体修饰T细胞
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Property Focused Structure-Based Optimization of Small Molecule Inhibitors of the Protein-Protein Interaction between Menin and Mixed Lineage Leukemia (MLL).基于结构的针对Menin与混合谱系白血病(MLL)蛋白-蛋白相互作用的小分子抑制剂的性质导向优化
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