Advantage of sorafenib combined with radiofrequency ablation for treatment of hepatocellular carcinoma

被引:9
|
作者
Tang, Zhe [1 ]
Kang, Muxing [1 ]
Zhang, Bo [1 ]
Chen, Jianke [2 ]
Fang, Heqing [1 ]
Ye, Qin [3 ]
Jiang, Biao [4 ]
Wu, Yulian [1 ]
机构
[1] Zhejiang Univ, Sch Med, Affiliated Hosp 2, Dept Surg, 88 Jiefang Rd, Hangzhou 310009, Zhejiang, Peoples R China
[2] Zhejiang Univ, Sch Med, Affiliated Hosp 2, Dept Ultrasound, Hangzhou, Zhejiang, Peoples R China
[3] Zhejiang Univ, Sch Med, Affiliated Hosp 2, Dept Pathol, Hangzhou, Zhejiang, Peoples R China
[4] Zhejiang Univ, Sch Med, Affiliated Hosp 2, Dept Radiol, Hangzhou, Zhejiang, Peoples R China
关键词
Hepatocellular carcinoma; Radiofrequency ablation; Sorafenib; Tumor perfusion; COMBINATION THERAPY; TUMOR ABLATION; BLOOD-FLOW; EFFICACY; TRIAL; VASCULATURE; SAFETY;
D O I
10.5301/tj.5000585
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Hepatocellular carcinoma (HCC) is a leading cause of death worldwide. Among the surgical and nonsurgical treatments available, radiofrequency ablation (RFA) and sorafenib have been shown to have efficacy. There is little evidence whether combination of these therapies would have additional benefits. Methods: In a mouse model of HCC, effects of sorafenib were determined by tumor size, RFA-induced necrosis area (triphenyltetrazolium chloride staining), microvascular density (MVD; 4', 6-diamidino-2-phenylindole and anti-CD31 antibody staining), and tumor perfusion (magnetic resonance imaging). Results: The RFA-induced necrosis area was 80.98 +/- 9.14 and 69.49 +/- 7.46 mm(2) in mice administered 80 and 40 mg/kg sorafenib, respectively, but only 57.29 +/- 3.39 mm(2) in controls. Sorafenib also reduced tumor volume and enhanced RFA-induced tumor destruction in a dose-dependent manner, and reduced both MVD and tumor perfusion. Conclusions: The results of our study suggest a potential role for combining RFA with sorafenib for treatment of HCC. Sorafenib could enhance RFA efficiency, possibly through its angiogenesis suppressive effects.
引用
收藏
页码:286 / 291
页数:6
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