The University of Texas, M.D. Anderson Cancer Center, Department of Leukemia , 1515 Holcombe Blvd. Box 428. Houston, TX 77030 , USA +1 713 792 4764 ; +1 713 794 4297 ;
Expert Opin Investig Drugs. 2014 Feb;23(2):255-63. doi: 10.1517/13543784.2014.877887.
Clofarabine is a second-generation purine nucleoside analog approved in 2004 for the treatment of pediatric patients with relapsed or refractory acute lymphocytic leukemia (ALL) following failure of at least two prior regimens. Clofarabine is a hybrid of fludarabine and cladribine, designed to overcome the pharmacologic limitations associated with its predecessors, while retaining their beneficial properties. In addition to providing a valuable treatment option for pediatric patients with ALL, clofarabine alone and in combination with cytarabine (Ara-C) has demonstrated substantial activity against myelodysplastic syndrome (MDS), thus rendering this agent a potential therapeutic option for MDS.
This review focuses on the pharmacology and clinical activity of clofarabine in MDS, as well as its emerging role in the treatment of MDS. Publications in English were selected from the MEDLINE (PubMed) database, as well articles of interest from bibliographies and abstracts based on the publication of meeting materials.
DNA-methyltransferase inhibitors are the mainstay of therapy for many patients with MDS who require treatment. Although these agents are very well tolerated and represent a significant advancement in the treatment of MDS by improving transfusion requirements and prolonging survival in various subgroups of patients, response rates are modest and the duration of response is short. In addition to providing a valuable treatment option for pediatric ALL patients, clofarabine has substantial activity against MDS and is well tolerated by elderly patients, thus rendering it a potential therapeutic option.
氯法拉滨是一种第二代嘌呤核苷类似物,于 2004 年批准用于治疗至少两种先前方案失败后复发或难治性儿童急性淋巴细胞白血病(ALL)的儿科患者。氯法拉滨是氟达拉滨和克拉屈滨的混合物,旨在克服与其前体相关的药物局限性,同时保留其有益特性。除了为 ALL 儿科患者提供有价值的治疗选择外,氯法拉滨单独或与阿糖胞苷(Ara-C)联合使用对骨髓增生异常综合征(MDS)具有显著活性,从而使该药物成为 MDS 的潜在治疗选择。
这篇综述重点介绍了氯法拉滨在 MDS 中的药理学和临床活性,以及它在 MDS 治疗中的新作用。在 MEDLINE(PubMed)数据库中选择了英文出版物,以及根据会议材料出版的相关文献和摘要中感兴趣的文章。
DNA 甲基转移酶抑制剂是许多需要治疗的 MDS 患者的主要治疗方法。尽管这些药物耐受性非常好,通过改善输血需求和延长各种亚组患者的生存时间,代表了 MDS 治疗的重大进展,但反应率较低,反应持续时间较短。除了为儿科 ALL 患者提供有价值的治疗选择外,氯法拉滨对 MDS 具有显著活性,且老年患者耐受性良好,因此成为一种潜在的治疗选择。