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Targeted therapy in leukemia

机译:白血病的靶向治疗

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Research conducted over the last two decades has yielded a detailed understanding of the molecular lesions that contribute to the malignant transformation of hematopoietic stem cells and committed progenitors into the various forms of acute and chronic leukemia. Although our understanding of the molecular pathology of leukemia remains incomplete, the information gained to date has had a profound impact on the way these malignancies are both diagnosed and monitored during therapy. More recently, targeted therapies have been developed against some of the identified genetic lesions. These therapies have led to significant improvements in patient outcomes while simultaneously decreasing therapy-related toxicity. With the advent of genome-wide methods to define the total complement of genetic and epigenetic lesions involved in leukemogenesis, new targeted therapies can be anticipated. This review highlights some of the targeted therapies that are presently being used to treat hematopoietic malignancies and describes some of the recent advances that should have a significant impact on the development of future target therapies.
机译:在过去的二十年中进行的研究已对导致造血干细胞和定型祖细胞恶性转化为各种形式的急性和慢性白血病的分子损伤进行了详细的了解。尽管我们对白血病分子病理学的理解仍然不完整,但迄今为止获得的信息对治疗期间诊断和监测这些恶性肿瘤的方式产生了深远的影响。最近,已经针对某些已鉴定的遗传损伤开发了靶向疗法。这些疗法在显着改善患者预后的同时,降低了与疗法相关的毒性。随着全基因组方法的出现,以定义涉及白血病发生的遗传和表观遗传损伤的全部补体,可以期待新的靶向疗法。这篇综述重点介绍了目前用于治疗造血系统恶性肿瘤的一些靶向疗法,并介绍了一些近期的进展,这些进展将对未来靶标疗法的发展产生重大影响。

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