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血液肿瘤分子靶向治疗现状

英文原题:Current Status of Molecularly Targeted Therapeutics in Blood Cancers.

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Current Status of Molecularly Targeted Therapeutics in Blood Cancers.

PubMed 2025/10/29(内容时间) Int J Mol Sci Q1 · IF 5.6(JCR 2025)

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中文摘要

血液癌症的特征是骨髓或淋巴系统中血细胞不受控制地生长。尽管化疗存在不良反应,但在多种类型的血液癌症中,化疗仍被视为一线治疗方法。近年来,对这些癌症病理学和基因组变化认识的进展,促进了新型药物靶点的发现和新治疗药物的开发。在这篇综述中,我们将讨论用于血液癌症的几类靶向治疗的作用机制和临床效用,包括不同类型酪氨酸激酶酶(BCR-ABL、FLT3 和 BTK)的抑制剂、BCL-2 抑制剂、磷脂酰肌醇 3-激酶抑制剂、核输出抑制剂、免疫疗法(单克隆抗体、放射免疫偶联物、CAR-T 细胞、免疫检查点抑制剂和双特异性抗体),以及蛋白酶体依赖性药物(蛋白酶体抑制剂和蛋白水解靶向嵌合体)。在识别血液癌症中不同分子亚群方面的进一步进展,将为新型靶向治疗和更个性化的医学方法提供更多机会。

展开英文摘要原文

Blood cancer is characterized by the uncontrolled growth of blood cells in the bone marrow or in the lymphatic system. Chemotherapy is still considered the first line of treatment in several types of blood cancer despite its adverse effects. Recent advances in understanding the pathology and genomic changes in these cancers have led to the discovery of novel drug targets and the development of new therapeutic agents.

In this review, we will discuss the mechanisms of action and clinical utility of several classes of targeted therapy used in blood cancers, including inhibitors of different types of tyrosine kinase enzymes (BCR-ABL, FLT3 and BTK), BCL-2 inhibitors, phosphoinositide 3-kinase inhibitors, nuclear export inhibitors, immune therapies (monoclonal antibodies, radioimmunoconjugates, chimeric antigen receptor T-cells, immune checkpoint inhibitors, and bispecific antibodies), and proteasome-dependent drugs (proteasome inhibitors and proteolysis targeting chimeras).

Further advances in identifying distinct molecular subgroups in blood cancers will offer more opportunities for novel targeted therapies and more personalized medicine approaches.

论文信息

作者
Kumala C、Vu L、Fandy TE
单位
Paul L. Foster School of Medicine, Texas Tech University Health Sciences Center El Paso, El Paso, TX 79905, USA.United States
文献类型
综述
期刊
International journal of molecular sciences2025 Oct 29
原文标识
PubMed 41226551 · DOI 10.3390/ijms262110512