Nitschke R, Komp D M, Morgan S K, Starling K A, Vietti T J
J Clin Pharmacol. 1978 Feb-Mar;18(2-3):131-5. doi: 10.1002/j.1552-4604.1978.tb02433.x.
In a toxicity study to determine the feasibility of treating patients with acute lymphocytic leukemia (ALL) using an intravenous combination of cytosine arabinoside (Ara-C) and methotrexate (MTX), the drugs were given either simultaneously or sequentially every two weeks. Twenty-nine patients were studied, 17 treated simultaneously, 12 treated sequentially. The tolerated doses of Ara-C and MTX were 60 mg/m2 and 90 mg/m2, respectively, for the simultaneous treatment schedule and 90 mg/m2 and 150 mg/m2, respectively, for the sequential treatment schedule. The dose-limiting factor of the drug combination was gastrointestinal toxicity. The observed recurrent vomiting on both schedules rendered the treatment unsuitable for maintenance therapy.
在一项毒性研究中,为确定使用阿糖胞苷(Ara-C)和甲氨蝶呤(MTX)静脉联合用药治疗急性淋巴细胞白血病(ALL)患者的可行性,药物每两周同时或序贯给药。共研究了29例患者,17例同时给药,12例序贯给药。对于同时给药方案,阿糖胞苷和甲氨蝶呤的耐受剂量分别为60mg/m²和90mg/m²;对于序贯给药方案,耐受剂量分别为90mg/m²和150mg/m²。药物联合的剂量限制因素是胃肠道毒性。两种给药方案中均观察到反复呕吐,使得该治疗不适用于维持治疗。