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Brivanib治疗肝癌的临床研究进展 被引量:4
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作者 祁兴顺 杨曼 +3 位作者 白苇 任维榕 樊代明 韩国宏 《临床肝胆病杂志》 CAS 2014年第3期222-224,共3页
Brivanib可同时抑制成纤维细胞生长因子受体(FGFR)-1、FGFR-2、FGFR-3、血管内皮细胞生长因子受体(VEGFR)-2和VEGFR-3,以达到抑制肿瘤新生血管形成及肿瘤细胞生长的作用。旨在总结Brivanib治疗肝癌的进展,已完成的Ⅰ和Ⅱ期临床试验结果... Brivanib可同时抑制成纤维细胞生长因子受体(FGFR)-1、FGFR-2、FGFR-3、血管内皮细胞生长因子受体(VEGFR)-2和VEGFR-3,以达到抑制肿瘤新生血管形成及肿瘤细胞生长的作用。旨在总结Brivanib治疗肝癌的进展,已完成的Ⅰ和Ⅱ期临床试验结果均证实了Brivanib在肝癌治疗中的安全性和有效性。然而,1项已完成的Ⅲ期随机双盲安慰剂对照研究表明,Brivanib作为晚期肝癌二线治疗手段(即Sorafenib治疗失败者)并未显著改善患者的总体生存期。另1项Ⅲ期随机双盲对照试验结果也表明,Brivanib作为晚期肝癌一线治疗手段并未比Sorafenib显著改善患者的总体生存期。这2项临床试验的失败使得其他两项有关Brivanib治疗肝癌的临床试验提前终止。通过分析以上研究认为亚组分析以及事先筛选Brivanib可能获益的肝癌患者(即FGF信号途径激活的肝癌患者)也许对进一步探究Brivanib的在肝癌治疗中的角色是必要的。 展开更多
关键词 肝肿瘤 brivanib 临床试验 综述
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Brivanib对HepG2细胞的抑制作用及机制 被引量:1
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作者 韩兴华 王章桂 《现代肿瘤医学》 CAS 2017年第3期355-357,共3页
目的:探讨Brivanib对人Hep G2肝癌细胞的增殖抑制作用及其机制。方法:MTS法检测Brivanib对Hep G2细胞的增殖抑制作用,流式细胞仪检测不同浓度Brivanib处理后Hep G2细胞的凋亡率,Western blot检测凋亡相关蛋白Bcl-2、Bax的表达情况,免疫... 目的:探讨Brivanib对人Hep G2肝癌细胞的增殖抑制作用及其机制。方法:MTS法检测Brivanib对Hep G2细胞的增殖抑制作用,流式细胞仪检测不同浓度Brivanib处理后Hep G2细胞的凋亡率,Western blot检测凋亡相关蛋白Bcl-2、Bax的表达情况,免疫荧光观察Brivanib处理后Hep G2细胞内源性LC3表达情况,Western blot检测自噬关键蛋白LC-I向LC-II的转换及p62的表达。结果:与空白对照组相比,Brivanib对Hep G2肝癌细胞的增殖抑制率随剂量增加和时间延长而增加,呈剂量和时间依赖性。不同浓度Brivanib作用72h后Hep G2细胞的凋亡率分别为(13.06±4.06)%、(20.89±1.83)%、(44.29±2.56)%,其诱导凋亡与下调Bax、上调Bcl-2表达相关。2.5μmol/L Brivanib处理Hep G2细胞48h后内源性LC3表达增加。Western blot分析表明,LC3-I向LC3-II转换增加,p62表达降低。结论:Brivanib抑制Hep G2人肝癌细胞增殖,诱导凋亡和自噬活化。 展开更多
关键词 肝细胞癌 brivanib 凋亡 自噬
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Chemotherapy and target therapy for hepatocellular carcinoma:New advances and challenges 被引量:31
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作者 Gan-Lu Deng Shan Zeng Hong Shen 《World Journal of Hepatology》 CAS 2015年第5期787-798,共12页
Primary liver cancer is one of the commonest causes of death.Hepatocellular carcinoma(HCC) accounts for 90% of primary liver cancers.For patients with unresectable or metastatic HCC,conventional chemotherapy is of lim... Primary liver cancer is one of the commonest causes of death.Hepatocellular carcinoma(HCC) accounts for 90% of primary liver cancers.For patients with unresectable or metastatic HCC,conventional chemotherapy is of limited or no benefit.Sorafenib is the only systemic treatment to demonstrate a statistically significant but modest overall survival benefit,leading to an era of targeted agents.Many clinical trials of targeted drugs have been carried out with many more in progress.Some drugs like PTK787 showed potential benefits in the treatment of HCC.Despite these promising breakthroughs,patients with HCC still have a dismal prognosis.Recently,both a phase Ⅲ trial of everolimus and a phase Ⅱ clinical trial of trebananib failed to demonstrate effective antitumor activity in advanced HCC.Sorafenib still plays a pivotal role in advanced HCC,leading to further explorations to exert its maximum efficacy.Combinations targeted with chemotherapy or transarterial chemoembolization is now being tested and might bring about advances.New targeted agents such as mammalian target of rapamycin inhibitors are under investigation,as well as further exploration of the mechanism of hepatocarcinogenesis. 展开更多
关键词 Hepatocellular carcinoma Ramucirumab REGORAFENIB Tivantinib Molecular targeted therapy SORAFENIB Linifanib ERLOTINIB EVEROLIMUS SUNITINIB brivanib
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Targeted systemic therapies for hepatocellular carcinoma:Clinical perspectives,challenges and implications 被引量:10
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作者 Catherine Frenette Robert Gish 《World Journal of Gastroenterology》 SCIE CAS CSCD 2012年第6期498-506,共9页
Hepatocellular carcinoma (HCC) is a lethal disease in most patients, due to its aggressive course and a lack of effective systemic therapies for advanced disease. Surgical resection and liver transplantation remain ... Hepatocellular carcinoma (HCC) is a lethal disease in most patients, due to its aggressive course and a lack of effective systemic therapies for advanced disease. Surgical resection and liver transplantation remain the only curative options for a small subset of patients. Few patients with HCC are diagnosed early enough to be eli- gible for curative treatment. Angiogenesis inhibition is a natural therapeutic target for all solid tumors, but par- ticularly for the highly vascularized HCC tumors. With the approval of the targeted agent sorafenib, there are now additional options for patients with HCC. Although sorafenib does produce some improvement in survival in HCC patients, the responses are not durable. In addi- tion, there are significant dermatologic, gastrointestinal, and metabolic toxicities, and, as importantly, there is still limited knowledge of its usefulness in special sub- populations with HCC. Other angiogenesis inhibitors are in development to treat HCC both in the first-line set- ting and for use following sorafenib failure; the furthest in development is brivanib, a dual fibroblast growth factor pathway and vascular endothelial growth factor receptor inhibitor. Additional agents with antiangiogenic properties also in phase IT and Ⅲ development for the treatment of patients with HCC include bevacizumab, ramucirumab, ABT-869, everolimus and ARQ 197. 展开更多
关键词 Hepatocellular carcinoma Angiogenesis Vas-cular endothelial growth factor Fibroblast growth factor SORAFENIB Tumor response brivanib
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抗肿瘤新药布立尼布的合成 被引量:1
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作者 孙敏 宗在伟 孙焕亮 《中国新药杂志》 CAS CSCD 北大核心 2012年第17期2065-2068,共4页
目的:合成抗肿瘤新药布立尼布,并对其工艺进行改进。方法:以3-甲基-1H-吡咯-2,4-二甲酸乙酯为原料,经N-氨基化,环合,格氏反应,氧化重排,乙酰化,卤化,亲核取代,脱保护和亲核取代反应制得布立尼布。结果与结论:目标产物结构经1H-NMR和MS确... 目的:合成抗肿瘤新药布立尼布,并对其工艺进行改进。方法:以3-甲基-1H-吡咯-2,4-二甲酸乙酯为原料,经N-氨基化,环合,格氏反应,氧化重排,乙酰化,卤化,亲核取代,脱保护和亲核取代反应制得布立尼布。结果与结论:目标产物结构经1H-NMR和MS确证,总收率为21.6%,ee值为99.3%。改进后的制备工艺反应条件温和,适合工业化生产。 展开更多
关键词 抗肿瘤药 布立尼布 合成
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