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Targeting angiogenesis driven by vascular endothelial growth factors using antibody-based therapies.

机译:使用基于抗体的疗法靶向由血管内皮生长因子驱动的血管生成。

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摘要

PURPOSE: Angiogenesis, one of the hallmarks of cancer, has recently become the target of therapeutic approaches in oncology. Among the complex system of pro- and antiangiogenic factors, the vascular endothelial growth factor system stands out as key mediator of tumor-initiated angiogenesis and as target of antiangiogenesis agents introduced in clinical practice. Although antivascular endothelial growth factor therapies, and in particular, bevacizumab as monoclonal antibody against vascular endothelial growth factor has clearly demonstrated antitumor efficacy, its mechanism of action is not fully understood. DESIGN: This review will discuss the rationale for using antiangiogenesis as anticancer therapy with focus on antibody-based approaches toward the vascular endothelial growth factor-system. Results of clinical trials using bevacizumab will be discussed in detail. RESULTS: Bevacizumab has well-documented efficacy as part of first-line therapy in various malignancies ranging from colorectal to breast and lung cancer. Although it mainly exerts its efficacy in conjunction with conventional cytotoxic chemotherapy, several, apparently vascular endothelial growth factor-dependent malignancies such as renal cell cancer, ovarian cancer, and glioblastoma have shown to be susceptible to single-agent bevacizumab. DISCUSSION: Antiangiogenesis therapy with antibodies, namely bevacizumab as antivascular endothelial growth factor agent, has demonstrated efficacy in various human malignancies. The mechanism of action of antivascular endothelial growth factor therapy in general and bevacizumab in particular, however, is not fully understood. Predictive markers have not yet been identified and questions regarding bevacizumab's usefulness in the adjuvant setting as well as its value as continued therapy beyond progression are still unanswered. It is indisputable, though, that antiangiogenesis has greatly enhanced the therapeutic arsenal of anticancer therapies and has changed oncology forever.
机译:目的:血管生成是癌症的标志之一,最近已成为肿瘤治疗方法的目标。在促血管生成因子和抗血管生成因子的复杂系统中,血管内皮生长因子系统是肿瘤引发的血管生成的关键介质和临床实践中引入的抗血管生成剂的靶点。尽管抗血管内皮生长因子疗法,特别是贝伐单抗作为抗血管内皮生长因子的单克隆抗体已明确显示出抗肿瘤功效,但其作用机理尚未完全明了。设计:本综述将讨论使用抗血管生成作为抗癌治疗的基本原理,重点是针对血管内皮生长因子系统的基于抗体的方法。将详细讨论使用贝伐单抗的临床试验结果。结果:贝伐单抗作为一线治疗的一部分,在从结肠直肠癌到乳腺癌和肺癌的各种恶性肿瘤中具有良好的疗效。尽管它主要与常规的细胞毒性化学疗法一起发挥功效,但已证明几种明显依赖血管内皮生长因子的恶性肿瘤(例如肾细胞癌,卵巢癌和成胶质细胞瘤)对单药贝伐单抗敏感。讨论:抗体即贝伐单抗作为抗血管内皮生长因子药物的抗血管生成治疗已证明对多种人类恶性肿瘤有效。一般而言,抗血管内皮生长因子疗法的作用机理,尤其是贝伐单抗的作用机理尚未完全了解。尚未鉴定出预测性标志物,关于贝伐单抗在佐剂中的有效性以及其在超过进展期的持续治疗中的价值仍未得到解答。毫无疑问,抗血管生成极大地增强了抗癌疗法的治疗能力,并永远改变了肿瘤学。

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