最近批准的AML分子靶向治疗

Nikolaos Papadantonakis, Harry P. Erba
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引用次数: 0

摘要

急性髓性白血病是一种疾病,直到最近,很少有选择可用于新诊断和复发/难治性患者。近年来,一些新药获得批准,为患者提供了更多的选择。令人鼓舞的是,这些新药物针对分子畸变/关键蛋白,使患者免受强化化疗方案的副作用。在这篇综述中,我们重点介绍了导致Glasdegib、Venetoclax、Enasidenib、Ivosidenib和Gilteritinib获批的研究,并重点介绍了关键的临床要点。我们还概述了新药物在临床实践中带来的挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recently approved molecularly targeted therapies in AML

Acute myeloid leukemia is a disease for which, until recently few options were available both for the newly diagnosed and relapsed/refractory patients. In the recent years, several new agents have been approved offering patients more options. Encouragingly, the new agents are targeting molecular aberrations/key proteins sparing the patients from the side effects of the intensive chemotherapy regimens. In this review, we highlight the studies leading to approval of Glasdegib, Venetoclax, Enasidenib, Ivosidenib, and Gilteritinib and we highlight key clinical points. We also outline the challenges that the new agents bring in the clinical practice.

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