持续皮下输注低剂量ara-C:药理学评价。

D R Spriggs, J E Sokal, J Griffin, D W Kufe
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引用次数: 4

摘要

低剂量ara-C已广泛应用于白血病前期和白血病的治疗。这些研究通常采用每日两次皮下注射方案或连续静脉输注方案。为了克服长期静脉输注的后勤问题,同时提供长时间的ara-C暴露,我们研究了持续皮下输注ara-C (20mg /M2/d)的药理学。在8例患者中获得的结果表明,持续皮下输注(24.6-65.6 nM)获得的稳态血浆ara-C水平与静脉输注(26.2-61.5 nM)获得的血浆ara-C水平无显著差异。皮下注射导致骨髓抑制延长,与连续静脉注射相似。通过皮下途径持续输注低剂量ara-C为一些门诊患者提供了一种治疗选择,与静脉输注相比具有优势,静脉输注通常需要放置静脉导管或住院治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Low dose ara-C administered by continuous subcutaneous infusion: a pharmacologic evaluation.

Low dose ara-C has been widely used in the treatment of preleukemia and leukemia. These studies have generally utilized either a twice daily, subcutaneous bolus schedule or a continuous intravenous infusion schedule. In order to surmount the logistical problems of long term intravenous infusion while providing prolonged ara-C exposure, we have studied the pharmacology of administering ara-C (20 mg/M2/d) by continuous subcutaneous infusion. The results obtained in eight patients demonstrate that steady state plasma ara-C levels achieved during continuous subcutaneous infusion (24.6-65.6 nM) are not significantly different than those obtained during intravenous infusions (26.2-61.5 nM). Subcutaneous infusions result in prolonged myelosuppression similar to that seen with continuous intravenous infusions. The continuous infusion of low dose ara-C by the subcutaneous route provides a treatment option for some outpatients and offers advantages over intravenous infusions which often require placement of venous catheters or hospitalization.

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