Unit of Hepatobiliary Surgery and Liver Transplantation, IMIBIC/Reina Sofia Hospital/University of Cordoba, Córdoba, Spain.
Clinical Analyses Service & Department of Biochemistry and Molecular Biology, IMIBIC/Reina Sofia Hospital/University of Cordoba, Córdoba, Spain.
Anticancer Agents Med Chem. 2019;19(11):1388-1398. doi: 10.2174/1871520619666190417162409.
Parallel to the safety of liver resections, new chemotherapy drugs have emerged for the control of liver metastases. However, there is unclear evidence about the combination of intensive BVZ-therapy and extended resections. The main aim was to analyse the impact of Bevacizumab (BVZ) in terms of liver safety and tolerability in two experimental models: a basal-toxicity situation and after major hepatectomy.
Eighty male-Wistar rats were grouped as toxicity analysis (sham-operated rats-OS-) and regeneration after- surgery analysis (hepatectomy rats-H-). Eight further subgroups were created according to sacrifice (6- hours-6h- or 24-hours-24h-) and dose (μg) of BVZ (none, 100, 200, 400). Several measurements were performed, including biochemical serum samples, histopathological analysis, cytokines (IL-6, TNF-α, TGF-β), oxidative-stress (GSH/GSSG, ATP), lipid-peroxidation (TBARS) and epidermal and vascular endothelium growth-factors (EGF and VEGF).
In the toxicity analysis, safe results with BVZ were observed, with no significant differences among the groups. A trend towards a lower oxidative status was observed in the OS 6 h-100, -200 and -400 versus the OS 6 h-none group. Similar results were observed in the hepatectomy model, with stable oxidative-stress-index and IL-6, TNF- α, and TGF- β levels. Despite higher lipid peroxidation status, overall regeneration was preserved. As expected, VEGF was almost undetectable in BVZ-treated groups after resection, but not in the non-resection group.
It was concluded that liver status was not impaired by BVZ even at the high-dose. Similarly, liver regeneration after extended hepatectomy in BVZ-treated animals was well-preserved. Extended liver resections may be encouraged in BVZ-treated patients due to its excellent tolerability and good liver regeneration status.
随着肝切除术安全性的提高,新的化疗药物也已出现用于控制肝转移。然而,关于密集型 BVZ 治疗与扩大切除术联合应用的证据尚不明确。主要目的是分析贝伐单抗(BVZ)在两种实验模型中对肝脏安全性和耐受性的影响:基础毒性情况和大肝切除术后。
80 只雄性 Wistar 大鼠分为毒性分析(假手术大鼠-OS-)和术后再生分析(肝切除术大鼠-H)。根据处死时间(6 小时-6h-或 24 小时-24h-)和 BVZ 剂量(μg)(无、100、200、400)进一步分为 8 个亚组。进行了多项测量,包括生化血清样本、组织病理学分析、细胞因子(IL-6、TNF-α、TGF-β)、氧化应激(GSH/GSSG、ATP)、脂质过氧化(TBARS)和表皮及血管内皮生长因子(EGF 和 VEGF)。
在毒性分析中,BVZ 表现出安全结果,各组间无显著差异。与 OS 6h-无组相比,OS 6h-100、-200 和-400 组的氧化状态呈下降趋势。肝切除术模型中也观察到类似的结果,氧化应激指数和 IL-6、TNF-α、TGF-β 水平稳定。尽管脂质过氧化状态较高,但总体再生得到了维持。如预期的那样,BVZ 治疗后切除组的 VEGF 几乎无法检测到,但在未切除组中仍可检测到。
即使在高剂量下,BVZ 也不会损害肝脏功能。同样,BVZ 治疗动物的大肝切除术后肝再生也得到了很好的维持。由于其良好的耐受性和良好的肝再生状态,在 BVZ 治疗的患者中可能会鼓励进行扩大肝切除术。