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处于临床三期及以后阶段的化合物。

Compounds in clinical Phase III and beyond.

作者信息

Kessler Torsten, Bayer Michael, Schwöppe Christian, Liersch Rüdiger, Mesters Rolf M, Berdel Wolfgang E

机构信息

Department of Medicine, Hematology and Oncology, University of Münster, Albert-Schweitzer-Strasse, 33, 48129, Münster, Germany.

出版信息

Recent Results Cancer Res. 2010;180:137-63. doi: 10.1007/978-3-540-78281-0_9.

Abstract

Targeted therapies against cancer have become more and more important. In particular, the inhibition of tumor angiogenesis and vascular targeting have been the focus of new treatment strategies. Numerous new substances were developed as angiogenesis inhibitors and evaluated in clinical trials for safety, tolerance, and efficacy. With positive study results, some of these molecules have already been approved for clinical use. For example, this is true for the vascular endothelial growth factor neutralizing antibody bevacizumab (BEV) in metastatic colorectal cancer, nonsmall cell lung cancer, renal cancer, and breast cancer. The tyrosine kinase (TK) inhibitors sorafenib and sunitinib have been approved for metastatic renal cancer as well as for hepatocellular carcinoma, and sunitinib has also been approved for gastrointestinal stroma tumors. In this chapter we try to give an overview of the substances currently investigated in Phase III studies and beyond with regard to antiangiogenesis in cancer therapy.

摘要

针对癌症的靶向治疗变得越来越重要。特别是,抑制肿瘤血管生成和血管靶向已成为新治疗策略的重点。众多新物质被开发为血管生成抑制剂,并在临床试验中评估其安全性、耐受性和疗效。随着研究结果呈阳性,其中一些分子已被批准用于临床。例如,血管内皮生长因子中和抗体贝伐单抗(BEV)在转移性结直肠癌、非小细胞肺癌、肾癌和乳腺癌中就是如此。酪氨酸激酶(TK)抑制剂索拉非尼和舒尼替尼已被批准用于转移性肾癌以及肝细胞癌,舒尼替尼也已被批准用于胃肠道间质瘤。在本章中,我们试图概述目前正在进行III期及以后研究的、用于癌症治疗抗血管生成的物质。

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