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日本肝细胞癌治疗的现状:经动脉化疗栓塞。

Current status of hepatocellular carcinoma treatment in Japan: transarterial chemoembolization.

机构信息

Department of Imaging Diagnosis and Interventional Radiology, Kanazawa University Graduate School of Medical Science, 13-1 Takara-machi, Kanazawa, Japan.

出版信息

Clin Drug Investig. 2012 Aug 8;32 Suppl 2:3-13. doi: 10.1007/BF03265492.

Abstract

Transarterial chemoembolization (TACE) is the gold standard of treatment for intermediate-stage hepatocellular carcinoma (HCC), and involves the administration of cytotoxic drugs, with or without lipiodol, by means of a catheter directly to the hepatic artery followed by the administration of embolizing agents such as spherical gelatin or polyvinyl alcohol particles. There are currently no global guidelines regarding the dose, choice or combination of cytotoxic agents for TACE; therefore it is difficult to compare data from different TACE studies. Superselective TACE with lipiodol is the primary TACE procedure that offers satisfactory levels of local control with a lower risk of complications. Approximately 40-70% of patients with HCC with tumours sized 4-5 cm or less attained complete tumour necrosis or remained local recurrence free for 3 years or longer following TACE. The early identification of unresponsiveness to TACE is important to allow for a timely switch to alternative therapies. The use of novel embolizing materials in TACE such as drug-eluting beads and radioembolization is likely to have beneficial effects. Indeed, the increase in angiogenic activity following TACE emphasizes the potential of TACE in combination with targeted molecular therapies such as the anti-angiogenesis inhibitor, sorafenib.

摘要

经导管肝动脉化疗栓塞术(TACE)是治疗中期肝细胞癌(HCC)的金标准,包括通过导管直接将细胞毒性药物(可联合或不联合碘油)注入肝动脉,然后注入栓塞剂,如球形明胶或聚乙烯醇颗粒。目前,对于 TACE 的剂量、细胞毒药物的选择或联合尚无全球指南,因此难以比较来自不同 TACE 研究的数据。超选择性 TACE 联合碘油是主要的 TACE 方法,可提供满意的局部控制水平,并发症风险较低。大约 40-70%的肿瘤大小为 4-5cm 或更小的 HCC 患者在 TACE 后完全肿瘤坏死或 3 年或更长时间内无局部复发。早期识别对 TACE 的无反应性对于及时转为替代疗法很重要。在 TACE 中使用新型栓塞材料,如载药微球和放射性栓塞,可能会产生有益的效果。事实上,TACE 后血管生成活性的增加强调了 TACE 与靶向分子治疗(如抗血管生成抑制剂索拉非尼)联合应用的潜力。

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