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对阿糖胞苷磷酸酯(YNK01)在一名对苯丁酸氮芥/泼尼松、氟达拉滨以及泼尼松龙/米托蒽醌治疗难治的慢性淋巴细胞白血病患者中的反应。

Response to cytarabine ocfosfate (YNK01) in a patient with chronic lymphocytic leukemia refractory to treatment with chlorambucil/prednisone, fludarabine, and prednimustine/mitoxantrone.

作者信息

Braess J, Kern W, Unterhalt M, Kaufmann C C, Ramsauer B, Schüssler M, Kaeser-Fröhlich A, Hiddemann W, Schleyer E

机构信息

Department of Internal Medicine, University of Göttingen, Germany.

出版信息

Ann Hematol. 1996 Oct;73(4):201-4. doi: 10.1007/s002770050229.

Abstract

Cytarabine ocfosfate (YNK01) is a novel orally applicable prodrug of cytosine arabinoside. Recent pharmacokinetic studies have revealed a prolonged release of the cytotoxic agent cytosine arabinoside (araC) from hepatocytes into the systemic circulation, resulting in a half-life of approximately 24 h for araC. The specific pharmacokinetic characteristics of cytarabine ocfosfate lead to a prolonged exposure of leukemic cells to this antineoplasstic agent during the 14-day cycle. the oral applicability during outpatient treatment and the sustained antineoplastic activity of araC against slowly proliferating leukemic B-cells suggest that cytarabine ocfosfate might be a useful drug in the treatment of chronic lymphocytic leukemia. Four years after diagnosis of B-CLL, a 50-year-old patient was started on cytarabine ocfosfate. Sequentially, the patient's disease had proved refractory to treatment with chlorambucil/prednisone (31 months), fludarabine (5 months), and prednimustine/mitoxantrone (3 months). These established regimens were discontinued because of increasing lymphocytosis, significant thrombocytopenia, and progressive B-symptoms. Following three cycles of cytarabine ocfosfate B-symptoms resolved, lymphadenopathy disappeared, and thrombocytopenia was significantly reduced. The patient has been free of these symptoms on a dosage of 1500 mg cytarabine ocfosfate/day (cycle of 14 days with intervals of 14-21 days) for 24 months and remains in an ongoing partial remission.

摘要

阿糖胞苷奥磷酯(YNK01)是一种新型的可口服应用的阿糖胞苷前药。最近的药代动力学研究表明,细胞毒性药物阿糖胞苷(araC)从肝细胞向体循环的释放延长,导致araC的半衰期约为24小时。阿糖胞苷奥磷酯的特定药代动力学特征导致白血病细胞在14天周期内长时间暴露于这种抗肿瘤药物。门诊治疗期间的口服适用性以及araC对缓慢增殖的白血病B细胞的持续抗肿瘤活性表明,阿糖胞苷奥磷酯可能是治疗慢性淋巴细胞白血病的一种有用药物。在诊断为B细胞慢性淋巴细胞白血病四年后,一名50岁患者开始使用阿糖胞苷奥磷酯治疗。在此之前,该患者的疾病已被证明对苯丁酸氮芥/泼尼松(31个月)、氟达拉滨(5个月)和泼尼松氮芥/米托蒽醌(3个月)治疗无效。由于淋巴细胞增多、严重血小板减少和进行性B症状加重,这些既定方案被停用。在接受三个周期的阿糖胞苷奥磷酯治疗后,B症状消失,淋巴结病消失,血小板减少症明显减轻。该患者以每天1500毫克阿糖胞苷奥磷酯的剂量(14天为一个周期,间隔14 - 21天)持续治疗24个月,一直没有出现这些症状,目前仍处于持续部分缓解状态。

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