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抗血管生成蛋白激酶抑制剂和血管破坏剂在癌症中的安全性和耐受性:重点关注胃肠道恶性肿瘤。

Safety and Tolerability of Anti-Angiogenic Protein Kinase Inhibitors and Vascular-Disrupting Agents in Cancer: Focus on Gastrointestinal Malignancies.

机构信息

Unit of Medical Oncology 1, Veneto Institute of Oncology IOV-IRCCS, Padua, Italy.

Department of Surgery, Oncology and Gastroenterology, University of Padua, Padua, Italy.

出版信息

Drug Saf. 2019 Feb;42(2):159-179. doi: 10.1007/s40264-018-0776-6.

Abstract

Angiogenesis is an essential process for tumor growth and metastasis. Inhibition of angiogenesis as an anticancer strategy has shown significant results in a plethora of tumors. Anti-angiogenic agents are currently part of many standard-of-care options for several metastatic gastrointestinal cancers. Bevacizumab, aflibercept, ramucirumab, and regorafenib have significantly improved both progression-free and overall survival in different lines of treatment in metastatic colorectal cancer. Second-line ramucirumab and third-line apatinib are effective anti-angiogenic treatments for patients with metastatic gastric cancer. Unfortunately, the anti-angiogenic strategy has major practical limitations: resistance inevitably develops through redundancy of signaling pathways and selection for subclonal populations adapted for hypoxic conditions. Anti-angiogenic agents may be more effective in combination therapies, with not only cytotoxics but also other emerging compounds in the anti-angiogenic class or in the separate class of the so-called vascular-disrupting agents. This review aims to provide an overview of the approved and "under development" anti-angiogenic compounds as well as the vascular-disrupting agents in the treatment of gastrointestinal cancers, focusing on the actual body of knowledge available on therapy challenges, pharmacodynamic and pharmacokinetic mechanisms, safety profiles, promising predictive biomarkers, and future perspectives.

摘要

血管生成是肿瘤生长和转移的必要过程。抑制血管生成作为一种抗癌策略,在多种肿瘤中已经显示出显著的效果。抗血管生成药物目前是多种转移性胃肠道癌症标准治疗方案的一部分。贝伐珠单抗、阿柏西普、雷莫芦单抗和瑞戈非尼在转移性结直肠癌的不同治疗线中显著提高了无进展生存期和总生存期。二线雷莫芦单抗和三线阿帕替尼是转移性胃癌患者有效的抗血管生成治疗药物。不幸的是,抗血管生成策略存在重大的实际限制:由于信号通路的冗余和对适应缺氧条件的亚克隆群体的选择,不可避免地会产生耐药性。抗血管生成药物在联合治疗中可能更有效,不仅与细胞毒性药物联合,还与抗血管生成类别的其他新兴化合物或所谓的血管破坏剂类别的单独化合物联合。本综述旨在概述胃肠道癌症治疗中已批准和“正在开发”的抗血管生成化合物以及血管破坏剂,重点介绍关于治疗挑战、药效学和药代动力学机制、安全性概况、有前途的预测生物标志物以及未来展望的现有知识。

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