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Antibody prodrugs for cancer

机译:癌症的抗体前药

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Introduction: The toxicity of potent new biological therapies for cancer has limited their utility. By improving tumor specificity, antibody prodrugs can widen or even create a therapeutic window for anticancer agents that are difficult or impossible to use otherwise because of poor tolerability. Areas covered: This review will describe the current status of the field of antibody prodrugs, focusing on Probody therapeutics, including the principles behind their design, application to a variety of different antibody-based therapies, preclinical examples of their activity and safety, and early results of Phase 1 trials. Expert opinion: Proof of concept for the antibody prodrug approach, which is defined as demonstration of potent antitumor activity with improved safety, has been extensively established preclinically as well as preliminarily in early clinical trials in human patients. However, experience with antibody prodrugs is limited, and important challenges remain. Principal among them are how to design the molecules to provide the most effective protection from toxicities while preserving efficacy, how to optimize clinical pharmacology, and how to determine which among the many possible clinical applications is the best use of this promising technology.
机译:介绍:巨大的癌症新生物疗法的毒性有限有限。通过改善肿瘤特异性,抗体前药可以扩大甚至为难以或不可能使用的抗癌剂而产生治疗窗口,因为耐受性差。涵盖的地区:本综述将描述抗体前药领域的现状,重点涉及概率治疗剂,包括其设计背后的原则,应用于各种不同抗体的疗法,其活动和安全的临床前示例,以及早期第1阶段试验的结果。专家意见:抗体前药方法的概念证明,其被定义为具有改善的安全性的有效抗肿瘤活性的证明,在人类患者的早期临床试验中被广泛建立了广泛的建立。然而,抗体前药的经验是有限的,并且仍然存在重要的挑战。其中委托人在于如何设计分子以提供毒性最有效的保护,同时保持疗效,如何优化临床药理学,以及如何确定许多可能的临床应用中的最佳技术。

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