Slevin M L, Joel S P, Whomsley R, Devenport K, Harvey V J, Osborne R J, Wrigley P F
Imperial Cancer Research Fund Department of Medical Oncology, St. Bartholomews Hospital, London, England.
Cancer Chemother Pharmacol. 1989;24(5):329-31. doi: 10.1007/BF00304768.
The effect of dose on the bioavailability of oral etoposide was investigated in ten patients with malignant mesothelioma who received single-agent etoposide as part of a phase II study. Etoposide pharmacokinetics were studied in each patient at oral dose levels of 100, 200, 300, 400 and 600 mg. At doses above 200 mg, the AUC and peak concentrations of etoposide were substantially lower than predictions based on the 100-mg dose. This study confirms previous observations that etoposide absorption is dose-dependent and that a mean bioavailability of approximately 50% cannot be assumed at total oral doses greater than 200 mg.
在一项II期研究中,对10例接受单药依托泊苷治疗的恶性间皮瘤患者,研究了剂量对口服依托泊苷生物利用度的影响。在每位患者中,分别以100、200、300、400和600 mg的口服剂量水平研究依托泊苷的药代动力学。在剂量高于200 mg时,依托泊苷的AUC和峰值浓度显著低于基于100 mg剂量的预测值。本研究证实了先前的观察结果,即依托泊苷的吸收具有剂量依赖性,并且在总口服剂量大于200 mg时,不能假定平均生物利用度约为50%。