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VM-26与阿糖胞苷联合化疗用于儿童淋巴细胞白血病初始诱导治疗失败的情况。

VM-26 and cytosine arabinoside combination chemotherapy for initial induction failures in childhood lymphocytic leukemia.

作者信息

Rivera G, Dahl G V, Bowman W P, Avery T L, Wood A, Aur R J

出版信息

Cancer. 1980 Oct 15;46(8):1727-30. doi: 10.1002/1097-0142(19801015)46:8<1727::aid-cncr2820460804>3.0.co;2-4.

Abstract

Combination chemotherapy with VM-26 and ara-C was given to 14 children with acute lymphocytic leukemia who had not responded to initial treatment with prednisone, vincristine, daunomycin, and asparaginase. Nine of these patients had also received ara-C. At diagnosis, five children were classified as having standard prognostic features and nine as being at high risk for treatment failure. The drug combination was administered by vein twice a week for four weeks at dosages of 165 mg/m2 for VM-26 and 300 mg/m2 for araC. Nine complete remissions, five in patients with high-risk leukemia, were induced with acceptable toxicity; all 9 subsequently were given continuation therapy with oral mercaptopurine and methotrexate. Four of the 9 patients have relapsed at 2--21 months. All treatment was stopped in 2 patients after 30 months of complete remission. Combinations of VM-26 and ara-C represent an alternative remission induction treatment for patients who fail to attain initial remission with agents of established effectiveness. These agents may especially benefit patients with prognostic features indicating a high risk of treatment failure.

摘要

对14例急性淋巴细胞白血病患儿进行了VM-26和阿糖胞苷联合化疗,这些患儿对泼尼松、长春新碱、柔红霉素和天冬酰胺酶的初始治疗无反应。其中9例患者也接受过阿糖胞苷治疗。诊断时,5名儿童被归类为具有标准预后特征,9名儿童被归类为治疗失败高危患者。该药物组合每周静脉给药两次,共四周,VM-26剂量为165mg/m²,阿糖胞苷剂量为300mg/m²。诱导出9例完全缓解,其中5例为高危白血病患者,毒性可接受;随后所有9例患者均接受口服巯嘌呤和甲氨蝶呤的维持治疗。9例患者中有4例在2至21个月时复发。2例患者在完全缓解30个月后停止了所有治疗。VM-26和阿糖胞苷联合用药是对使用已证实有效的药物未能获得初始缓解的患者的一种替代缓解诱导治疗方法。这些药物可能对具有提示治疗失败高危预后特征的患者特别有益。

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