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酮康唑在血液系统恶性肿瘤成年患者长期给药期间的药代动力学

Ketoconazole pharmacokinetics during chronic dosing in adults with haematological malignancy.

作者信息

Stockley R J, Daneshmend T K, Bredow M T, Warnock D W, Richardson M D, Slade R R

出版信息

Eur J Clin Microbiol. 1986 Oct;5(5):513-7. doi: 10.1007/BF02017693.

Abstract

Ketoconazole pharmacokinetics were determined in nine adults with haematological malignancy after one week on a 200 mg daily dose and later after one week on a 400 mg daily dose. The area under the serum concentration time curve (AUC) reached 12.3 +/- 7.7 mg/l.h (mean +/- S.D.) on the 200 mg dose and increased to 23.0 +/- 18.2 mg/l.h on the 400 mg dose (p less than 0.05). The half-life of ketoconazole was 3.1 +/- 1.9 h on the 200 mg dose and 3.5 +/- 1.7 h on the 400 mg dose. Peak concentrations were 3.2 +/- 1.8 mg/l and 4.6 +/- 3.2 mg/l on the 200 mg and 400 mg doses, respectively. Trough ketoconazole concentrations were undetectable 24 h after either dose. There was no correlation between the leucocyte count and any pharmacokinetic parameter for ketoconazole. Variation in AUC was 20-fold on the 200 mg daily dose and 8-fold on the 400 mg per day regimen. Measurement of serum levels during ketoconazole treatment appears necessary in view of the unpredictable concentrations achieved. Once-a-day dosage regimens of ketoconazole in immunocompromised patients may be inappropriate. Future clinical trials should adopt a two or three times a day dosing regimen, as this may confer a pharmacokinetic and therapeutic advantage.

摘要

在9名血液系统恶性肿瘤成年患者中,测定了酮康唑的药代动力学。这些患者先接受每日200毫克剂量治疗一周,之后接受每日400毫克剂量治疗一周。血清浓度-时间曲线下面积(AUC)在200毫克剂量时达到12.3±7.7毫克/升·小时(均值±标准差),在400毫克剂量时增至23.0±18.2毫克/升·小时(p<0.05)。酮康唑在200毫克剂量时的半衰期为3.1±1.9小时,在400毫克剂量时为3.5±1.7小时。200毫克和400毫克剂量时的峰值浓度分别为3.2±1.8毫克/升和4.6±3.2毫克/升。两种剂量给药24小时后均未检测到酮康唑谷浓度。白细胞计数与酮康唑的任何药代动力学参数之间均无相关性。每日200毫克剂量时AUC的变化为20倍,每日400毫克方案时为8倍。鉴于酮康唑治疗期间达到的浓度不可预测,测定血清水平似乎很有必要。免疫功能低下患者每日一次的酮康唑给药方案可能不合适。未来的临床试验应采用每日两到三次的给药方案,因为这可能在药代动力学和治疗方面具有优势。

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