Delauter B J, Ramanathan R K, Egorin M J, Stover L L, Zuhowski E G, Plunkett W, Zamboni W C
Department of Pharmaceutical Sciences, School of Pharmacy, University of Pittsburgh, Pennsylvania, USA.
Pharmacotherapy. 2000 Oct;20(10):1204-7. doi: 10.1592/phco.20.15.1204.34586.
Gemcitabine (dFdC) is a prodrug that undergoes metabolism by cytidine deaminase to form an inactive metabolite, 2',2'-difluorodeoxyuridine (dFdU). The pharmacokinetics of dFdC and dFdU have been studied; however, their disposition has never been evaluated in a patient with ascites. A patient with pancreatic cancer and malignant ascites was treated with dFdC 1,500 mg/m2 over 150 minutes weekly for 3 weeks, repeated every 4 weeks. Serial plasma and ascites samples were obtained on weeks 1 and 2 of cycle 2. High-pressure liquid chromatography was used to quantify dFdC and dFdU in plasma and ascites. The systemic dispositions of dFdC and dFdU were similar to those reported in patients without ascites. The concentration of dFdC in ascites approached 1 mg/ml. Ascitic fluid did not serve as a depot for dFdC, and the agent's concentration in ascites approached that at which its phosphorylation is saturated.
吉西他滨(dFdC)是一种前体药物,通过胞苷脱氨酶代谢形成无活性代谢物2',2'-二氟脱氧尿苷(dFdU)。已对dFdC和dFdU的药代动力学进行了研究;然而,从未在腹水患者中评估过它们的处置情况。一名患有胰腺癌和恶性腹水的患者接受了dFdC治疗,剂量为1500mg/m²,每周静脉输注150分钟,共3周,每4周重复一次。在第2周期的第1周和第2周采集系列血浆和腹水样本。采用高压液相色谱法对血浆和腹水中的dFdC和dFdU进行定量。dFdC和dFdU的全身处置情况与无腹水患者的报道相似。腹水中dFdC的浓度接近1mg/ml。腹水并非dFdC的储存库,该药物在腹水中的浓度接近其磷酸化饱和时的浓度。