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综述文章:索拉非尼及其他口服药物治疗肝细胞癌的药理学疗法

Review article: pharmacological therapy for hepatocellular carcinoma with sorafenib and other oral agents.

作者信息

Chaparro M, González Moreno L, Trapero-Marugán M, Medina J, Moreno-Otero R

机构信息

Department of Hepatology and Ciberehd, University Hospital La Princesa, Universidad Autónoma de Madrid, Madrid, Spain.

出版信息

Aliment Pharmacol Ther. 2008 Dec 1;28(11-12):1269-77. doi: 10.1111/j.1365-2036.2008.03857.x. Epub 2008 Sep 20.

Abstract

BACKGROUND

Hepatocellular carcinoma (HCC) is the fifth most common malignancy worldwide. Unresectable disease patients have median survival of few months. There is a substantial need for novel treatments for patients with advanced HCC.

AIM

To provide an update review of mechanism of hepatocarcinigenesis and systemic therapies for HCC and the relevant role of Sorafenib in patients with advanced disease.

METHODS

A Medline search was performed to identify pertinent original research and review articles. Selected references in these articles were also evaluated.

RESULTS

Systemic chemotherapy for HCC has been quite ineffective. Preclinical studies demonstrated that Raf/MAPK-ERK kinase (MEK)/Extracellular signal regulated kinase (ERK) pathway has a role in HCC. HCC tumours are highly vascularized and vascular endothelial growth factor (VEGF) augments HCC development and metastasis. Sorafenib blocks tumour cell proliferation by targeting Raf/MEK/ERK signalling and exerts an antiangiogenic effect by targeting VEGF receptors-2/3 and platelet derived growth factor receptor beta tyrosine kinases.

CONCLUSIONS

Currently available therapies are not effective for patients with advanced HCC. Sorafenib has demonstrated for the first time to prolong survival in patients with advanced HCC, and it is the new reference standard for systemic treatment in these patients.

摘要

背景

肝细胞癌(HCC)是全球第五大常见恶性肿瘤。无法切除的患者中位生存期仅数月。晚期HCC患者对新型治疗方法有巨大需求。

目的

对肝癌发生机制、HCC的全身治疗以及索拉非尼在晚期疾病患者中的相关作用进行最新综述。

方法

进行Medline检索以识别相关的原始研究和综述文章。还对这些文章中选定的参考文献进行了评估。

结果

HCC的全身化疗效果一直不佳。临床前研究表明,Raf/丝裂原活化蛋白激酶-细胞外信号调节激酶(MEK)/细胞外信号调节激酶(ERK)通路在HCC中起作用。HCC肿瘤血管高度丰富,血管内皮生长因子(VEGF)促进HCC的发展和转移。索拉非尼通过靶向Raf/MEK/ERK信号传导阻断肿瘤细胞增殖,并通过靶向VEGF受体-2/3和血小板衍生生长因子受体β酪氨酸激酶发挥抗血管生成作用。

结论

目前可用的治疗方法对晚期HCC患者无效。索拉非尼首次证明可延长晚期HCC患者的生存期,并且是这些患者全身治疗的新参考标准。

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