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Concise drug review: Azacitidine and decitabine

机译:简明药物审查:阿扎胞苷和地西他滨

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The hypomethylating agents azacitidine and decitabine (5-aza-2'-deoxycytidine) are currently approved for the treatment of several specific forms of myelodysplastic syndromes (MDS), chronic myelomonocytic leukemia (CMML), and acute myeloid leukemia (AML), as depicted in Table 1.The only potentially curative therapy for patients with higher-risk MDS (International Prognostic Scoring System intermedi-ate-2 risk and high risk) is an allogeneic stem cell transplantation (allo-SCT). However, for the majority of patients, allo-SCT is not an option because of advanced age and/or comorbidities. In addition, the results obtained with intensive chemotherapy (when feasible) are often disappointing. For patients with MDS, the probability of complete remission after intensive chemotherapy is generally lower and the remission duration shorterthan for patients with primary AML [1]. Therefore, the introduction of the hypomethylating agents has been a major advancement in the treatment of patients with higher-risk M DS who are ineligible for allo-SCT. Table 2 summarizes the key pharmacologic features of these two agents.
机译:如图所示,低甲基化剂阿扎胞苷和地西他滨(5-氮杂-2'-脱氧胞苷)目前已被批准用于治疗多种特定形式的骨髓增生异常综合症(MDS),慢性粒细胞性白血病(CMML)和急性髓性白血病(AML)。在表1中但是,对于大多数患者,由于年龄大和/或合并症,不能选择allo-SCT。此外,强化化疗(可行时)获得的结果通常令人失望。对于MDS患者,强化化疗后完全缓解的可能性通常比原发性AML患者低,且缓解时间较短[1]。因此,引入次甲基化剂已成为治疗不适合异种SCT的高危MDS患者的主要进展。表2总结了这两种药物的关键药理特性。

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