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VEGF/VEGFR 通路抑制剂治疗所致类别副作用的分子基础。

The molecular basis of class side effects due to treatment with inhibitors of the VEGF/VEGFR pathway.

作者信息

Roodhart Jeanine M, Langenberg Marlies H, Witteveen Els, Voest Emile E

机构信息

Department of Medical Oncology (F02.126), University Medical Center Utrecht, Utrecht, The Netherlands.

出版信息

Curr Clin Pharmacol. 2008 May;3(2):132-43. doi: 10.2174/157488408784293705.

Abstract

UNLABELLED

Vascular Endothelial Growth Factor (VEGF) is considered to be one of the most important regulators of angiogenesis and a new key target in anti-cancer treatment. Various clinical trials have validated the clinical importance of anti-VEGF or anti-VEGF receptor (VEGFR) therapy. Currently the humanized monoclonal antibody bevacizumab (blocks VEGF-A), and the tyrosine kinase inhibitors sunitinib and sorafenib (inhibit VEGFRs) are approved for patients with various malignancies and several others are expected in the coming years. Unfortunately, anti-VEGF/VEGFR treatment is not void of side effects. An array of unexpected side effects is now seen in clinical practice. Management of these side effects is extremely important in the development of the various anti-VEGF/VEGFR therapies and their optimal use. This review provides an overview of the toxicity profile of this class of agents, the molecular basis behind these side effects and indicates potential options for management. VEGF and its receptors play an important role in normal tissues and are widely expressed. It is likely that interference with this pathway induces an array of side effects due to the lack of normal function of VEGF. A consistent pattern of side effects is now emerging. Hypertension, gastro-intestinal toxicity, hypothyroidism, proteinuria, coagulation disorders and neurotoxicity are side effects observed with both anti-VEGF and anti-VEGFR inhibitors. For these side effects the role of VEGF/VEGFR pathway in normal tissue was reviewed in order to provide a molecular mechanism that linked side effect with physiological activity of VEGF/VEGFR. Insight into the molecular basis may aid specific supportive care measures to ensure optimal use of this class of agents.

CONCLUSION

Inhibiting the VEGF/VEGFR pathway is an effective approach to treat cancer. It has also provided new insight into the physiological role of this pathway in various organs. Integrating the knowledge in daily oncological practice will be a challenge for the future.

摘要

未标记

血管内皮生长因子(VEGF)被认为是血管生成最重要的调节因子之一,也是抗癌治疗的一个新的关键靶点。各种临床试验已经证实了抗VEGF或抗VEGF受体(VEGFR)治疗的临床重要性。目前,人源化单克隆抗体贝伐单抗(阻断VEGF-A)以及酪氨酸激酶抑制剂舒尼替尼和索拉非尼(抑制VEGFRs)已被批准用于治疗各种恶性肿瘤患者,预计未来几年还会有其他几种药物获批。不幸的是,抗VEGF/VEGFR治疗并非没有副作用。目前在临床实践中出现了一系列意想不到的副作用。在各种抗VEGF/VEGFR治疗方法的开发及其最佳应用中,对这些副作用的管理极为重要。本综述概述了这类药物的毒性特征、这些副作用背后的分子基础,并指出了潜在的管理方案。VEGF及其受体在正常组织中发挥重要作用且广泛表达。由于VEGF缺乏正常功能,干扰这一途径可能会引发一系列副作用。现在一种一致的副作用模式正在显现。高血压、胃肠道毒性、甲状腺功能减退、蛋白尿、凝血障碍和神经毒性是抗VEGF和抗VEGFR抑制剂都观察到的副作用。针对这些副作用,我们回顾了VEGF/VEGFR途径在正常组织中的作用,以便提供一种将副作用与VEGF/VEGFR的生理活性联系起来的分子机制。深入了解分子基础可能有助于采取特定的支持性护理措施,以确保这类药物的最佳应用。

结论

抑制VEGF/VEGFR途径是治疗癌症的有效方法。它也为该途径在各个器官中的生理作用提供了新的见解。将这些知识整合到日常肿瘤学实践中将是未来的一项挑战。

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