Arwanih Elly Y, Louisa Melva, Rinaldi Ikhwan, Wanandi Septelia I
Doctoral Program in Biomedical Sciences, Faculty of Medicine, Universitas Indonesia, Jakarta, IDN.
Pharmacology and Therapeutics, Faculty of Medicine, Universitas Indonesia, Jakarta, IDN.
Cureus. 2022 Dec 31;14(12):e33165. doi: 10.7759/cureus.33165. eCollection 2022 Dec.
Acute myeloid leukemia (AML) is a hematological malignancy commonly found in adult patients. Low overall survival and resistance to therapy are the main issues in AML. The first line of treatment for AML chemotherapy is the induction phase, namely, the phase to induce remission by administering a combination of daunorubicin (DNR) for three days followed by administration of cytarabine (Ara-C) with continuous infusion for seven days, which is referred to as "3 + 7." Such induction therapy has been the standard therapy for AML for the last four decades. This review article is made to discuss daunorubicin and cytarabine from their chemical structure, pharmacodynamics, pharmacokinetics, and mechanisms of resistance in AML.
急性髓系白血病(AML)是一种常见于成年患者的血液系统恶性肿瘤。总生存率低和对治疗的耐药性是AML的主要问题。AML化疗的一线治疗是诱导期,即通过连续三天给予柔红霉素(DNR),然后连续七天持续输注阿糖胞苷(Ara-C)来诱导缓解的阶段,这被称为“3 + 7”。在过去的四十年里,这种诱导治疗一直是AML的标准治疗方法。这篇综述文章旨在从柔红霉素和阿糖胞苷的化学结构、药效学、药代动力学以及AML的耐药机制方面进行讨论。