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Effects of bevadzumab on plasma concentration of irinotecan and its metabolites in advanced colorectal cancer patients receiving FOLFIRI with bevacizumab as second-line chemotherapy

机译:Bevadzumab对晚期结直肠癌血浆血浆血浆血浆浓度及其在北伐单抗作为二线化疗中的氨基屈氏癌患者血浆浓度及其代谢物

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Purpose Bevacizumab (BV) prolongs the survival of colorectal cancer patients when combined with irinotecan (CPT-11)-based regimens. In the AVF2107g study, the area under the curve (AUC) ratio for bolus CPT-11/5-fluorouracil (5-FU)/leucovorin (LV) (IFL) with the BV arm to bolus IFL with placebo indicated that SN-38 concentrations may have been increased in subjects receiving BV. However, the mechanism underlying such increase remains unclear, and the difference might be caused by an imbalance between the two arms and a possible inter-subject variability of CPT-11 metabolism. Within-subject comparisons were used to evaluate the effect of B V on advanced colorectal cancer patients when administered with the FOLFIRI regimen as second-line chemotherapy. Methods Ten advanced colorectal cancer patients received the FOLFIRI regimen every 2 weeks. At cycle 1, BV was administered following FOLFIRI administration to allow baseline pharmacokinetic (PK) analysis of CPT-11 and its metabolites. From cycle 2, BV was administered just before FOLFIRI administration. Plasma samples were collected under the same condition (at cycle 3). Results There were no significant differences in the C_(max) and AUC_(0-infinity) of CPT-11, SN-38, and SN-38G between cycle 1 (without BV) and cycle 3 (with BV). PK parameters of CPT-11, SN-38, and SN-38G were not significantly affected by BV. There were no significant differences in the changes in the AUC ratio of CPT-11 to SN-38 between cycles 1 and 3, as well as in the ratio of SN-38 to SN-38G. Conclusion BV does not affect the plasma concentration of CPT-11 and its metabolites on FOLFIRI regimen.
机译:目的,贝伐单抗(BV)延长结合伊替康(CPT-11)的方案时结肠直肠癌患者的存活。在AVF2107G研究中,用BV臂与安慰剂的BV臂(AUC)/ Leucovorin(IFL)下的曲线(AUC)/ Leucovorin(IFL)的面积表示SN-38在接受BV的受试者中可能增加浓度。然而,这种增加的机制仍然不清楚,并且差异可能是由两个臂之间的不平衡和CPT-11代谢的可能性间变异性引起。在对象内比较,用于评估B V在作为二线化疗中的Folfiri方案施用时对晚期结肠直肠癌患者的影响。方法治疗10例高级结肠直肠癌患者每2周接受Folfiri方案。在循环1,在Folfiri施用后施用BV以允许CPT-11及其代谢物的基线药代动力学(PK)分析。从循环2,BV在Folfiri管理之前施用。在相同条件下收集等离子体样品(在循环3)下。结果CPT-11,SN-38和SN-38G之间的C_(MAX)和AUC_(0-Infinity)没有显着差异(无BV)和循环3(用BV)。 CPT-11,SN-38和SN-38G的PK参数没有受BV的显着影响。 CPT-11至Sn-38之间的AUC比的变化没有显着差异,循环1和3之间,以及Sn-38与Sn-38G的比率。结论BV不影响CPT-11的血浆浓度及其代谢物对Folfiri方案。

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