HCC and angiogenesis: possible targets and future directions

索拉非尼 医学 肝细胞癌 全身疗法 血管生成 肿瘤微环境 肿瘤科 六氯环己烷 抗血管生成治疗 内科学 癌症研究 癌症 乳腺癌
作者
Andrew X. Zhu,Dan G. Duda,Dushyant V. Sahani,Rakesh K. Jain
出处
期刊:Nature Reviews Clinical Oncology [Springer Nature]
卷期号:8 (5): 292-301 被引量:511
标识
DOI:10.1038/nrclinonc.2011.30
摘要

Hepatocellular carcinoma (HCC) is notoriously resistant to systemic therapies. The success of the anti-VEGF therapy sorafenib in patients with advanced-stage HCC raises hope as well as critical questions on the future development of targeted agents including other antiangiogenic drugs. Hepatocellular carcinoma (HCC), the most common primary liver tumor, is notoriously resistant to systemic therapies, and often recurs even after aggressive local therapies. HCCs rely on the formation of new blood vessels for growth, and VEGF is critical in this process. A hallmark of new vessel formation in tumors is their structural and functional abnormality. This leads to an abnormal tumor microenvironment characterized by low oxygen tension. The liver is perfused by both arterial and venous blood and the resulting abnormal microenvironment selects for more-aggressive malignancies. Anti-VEGF therapy with sorafenib was the first systemic therapy to demonstrate improved survival in patients with advanced-stage HCC. This important development in the treatment of HCC raises hope as well as critical questions on the future development of targeted agents including other antiangiogenic agents, which hold promise to further increase survival in this aggressive disease.

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