Badrudin D, Sideris L, Leblond F A, Pichette V, Cloutier A S, Drolet P, Dubé P
Maisonneuve-Rosemont Research Center, Maisonneuve-Rosemont Hospital, Université de Montréal, Montreal QC, Canada.
Maisonneuve-Rosemont Research Center, Maisonneuve-Rosemont Hospital, Université de Montréal, Montreal QC, Canada.
Surg Oncol. 2018 Jun;27(2):275-279. doi: 10.1016/j.suronc.2018.05.004. Epub 2018 May 6.
Cytoreductive surgery and hyperthermic intraperitoneal chemotherapy (HIPEC) with oxaliplatin (OX) is the standard of care for selected patients with peritoneal carcinomatosis of colorectal origin. Because 5-FU is mandatory to improve efficacy of OX when used by systemic route, several teams now empirically combine intravenous (IV) 5-FU with HIPEC OX, but this practice has yet to be supported by preclinical data. Using a murine model, we studied the impact of IV 5-FU on peritoneal absorption of HIPEC OX.
Under general anesthesia, 24 Sprague-Dawley rats were submitted to 4 different doses of IV 5-FU (0, 100, 400 and 800 mg/m) and a fixed dose of HIPEC OX (460 mg/m) perfused at 40 °C during 25 min. At 25 min, samples in different compartments were harvested (peritoneum, portal vein and systemic blood) and the concentrations of 5-FU and OX were measured by high performance liquid chromatography.
Peritoneal absorption of OX was significantly higher (17.0, 20.1, 34.9 and 38.1 nmol/g, p < 0.0001) with increasing doses of 5-FU (0, 100, 400 and 800 mg/m, respectively). Peritoneal absorption of OX reached a plateau between 400 and 800 mg/m of IV 5-FU.
IV 5-FU enhances peritoneal absorption of HIPEC OX. The most efficient dose of IV 5-FU to be used in combination with HIPEC OX seems to be 400 mg/m.
细胞减灭术联合奥沙利铂(OX)的热灌注化疗(HIPEC)是特定结直肠来源腹膜转移癌患者的标准治疗方案。由于全身应用OX时,5-氟尿嘧啶(5-FU)是提高疗效的必需药物,目前有几个团队经验性地将静脉注射(IV)5-FU与HIPEC OX联合使用,但这一做法尚未得到临床前数据的支持。我们使用小鼠模型,研究了IV 5-FU对HIPEC OX腹膜吸收的影响。
在全身麻醉下,24只Sprague-Dawley大鼠接受4种不同剂量的IV 5-FU(0、100、400和800mg/m)以及固定剂量的HIPEC OX(460mg/m),于40℃灌注25分钟。在25分钟时,采集不同腔室的样本(腹膜、门静脉和全身血液),并通过高效液相色谱法测量5-FU和OX的浓度。
随着5-FU剂量增加(分别为0、100、400和800mg/m),OX的腹膜吸收显著增加(分别为17.0、20.1、34.9和38.1nmol/g,p<0.0001)。OX的腹膜吸收在IV 5-FU剂量为400至800mg/m之间达到平台期。
IV 5-FU可增强HIPEC OX的腹膜吸收。与HIPEC OX联合使用时,IV 5-FU的最有效剂量似乎为400mg/m。