Effect of Homoharringtonine as a Combined Regimen for Acute Myeloid Leukemia

IF 0.4 Q4 PHARMACOLOGY & PHARMACY Journal of Pharmacology & Pharmacotherapeutics Pub Date : 2021-07-01 DOI:10.4103/jpp.jpp_52_21
Abinaya Muralidharan, J. Scott, L. Joseph, S. Jeyabalan
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Abstract

Homoharringtonine (HHT), a cephalotaxus alkaloid has shown promising results in the treatment of several hematological disorders such as chronic myeloid leukemia, acute myeloid leukemia (AML), and myelodysplastic syndrome. It is known for its unique mechanism of action by which it prevents the initial elongation step of protein biosynthesis. Hence, it is used in hematological malignancies where it synergistically potentiates the action of other drugs and induces apoptosis. The relevant studies published were searched using an electronic database from 2002 to 2019. The articles published in English were only considered. Search engines such as PubMed, MEDLINE, Google Scholar, and Semantic scholar were used. In this review, we have discussed the effect of HHT in combination with other chemotherapeutic agents for AML with or without genetic mutation specification and the future perspective of these regimens. Although standard treatment options exist for most of these diseases, still cure rates are low with reported morbidity and the drug resistance emergence is pervasive. Thus, novel treatment approaches are crucial for better outcome. Alternative regimens together with HHT have not been a standard practice, although they have shown a very good potential in AML patients. Many of the combinations were also proved to be safe and effective with very low toxic potential. All these data outcomes of various combinations under different scenarios exhibit that HHT has promising results in the treatment of AML which may lead to its approval in the upcoming years.
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高三尖杉酯碱联合方案治疗急性髓细胞白血病疗效观察
高三尖杉酯碱(HHT)是一种三尖杉酯生物碱,在治疗慢性粒细胞白血病、急性粒细胞白血病(AML)和骨髓增生异常综合征等多种血液病方面显示出良好的疗效。它以其独特的作用机制而闻名,通过它可以阻止蛋白质生物合成的初始延伸步骤。因此,它被用于血液系统恶性肿瘤,协同增强其他药物的作用并诱导细胞凋亡。使用电子数据库检索了2002年至2019年发表的相关研究。只考虑了以英文发表的文章。使用了PubMed、MEDLINE、Google Scholar和Semantic Scholar等搜索引擎。在这篇综述中,我们讨论了HHT与其他化疗药物联合治疗具有或不具有遗传突变规范的AML的效果,以及这些方案的未来前景。尽管大多数这些疾病都有标准的治疗方案,但治愈率仍然很低,据报道发病率很低,耐药性的出现也很普遍。因此,新的治疗方法对于更好的结果至关重要。替代方案与HHT并不是一种标准做法,尽管它们在AML患者中显示出了很好的潜力。许多组合也被证明是安全有效的,毒性很低。不同情景下各种组合的所有这些数据结果表明,HHT在治疗AML方面具有良好的效果,这可能会在未来几年获得批准。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
0.40
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37
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