AML分子格局的变化及其对治疗的影响

L. Finn, C. Davis, Michael J Lunski, Muhammad Azeem Khan, A. Staton, Ambuga R. Badari
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引用次数: 1

摘要

急性髓性白血病是影响成人的原发性急性白血病,直到最近,可用的治疗选择非常有限。我们现在看到急性髓性白血病靶向治疗的发展和再开发,随后在疾病控制和总生存率方面有所改善。分子靶点疗法的发展使得那些不适合化疗的病人也能接受治疗。在这篇综述中,我们讨论了分子突变FLT3和IDH以及分子靶点CD33,它们在急性髓性白血病的发展中被认为具有关键作用。我们参考关键的临床试验来进一步讨论针对这些分子突变的急性髓性白血病的批准治疗方法。然后,我们讨论正在进行的研究,以开发新的药物和新的治疗组合,以克服耐药机制,进一步改善患者的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The changing molecular landscape of AML and its impact on treatment
Acute myeloid leukemia is the primary acute leukemia affecting adults and until recently had very limited available treatment options. We are now seeing development and redevelopment of targeted therapy in acute myeloid leukemia with subsequent improvements in disease control and overall survival. The development of therapy with molecular targets allows patients who are not candidates for chemotherapy to receive treatment. In this review, we discuss the molecular mutations FLT3 and IDH and the molecular target CD33, recognized for having key roles in the development of acute myeloid leukemia. We reference key clinical trials to further discuss the approved treatments for acute myeloid leukemia that target these molecular mutations. We then discuss ongoing research to develop new drugs and new combinations of therapy to overcome resistance mechanisms and further improve patient outcomes.
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