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抗体药物偶联物在癌症治疗中的应用。

Antibody-Drug Conjugates for Cancer Treatment.

机构信息

ImmunoGen, Inc., Waltham, Massachusetts 02451; email:

出版信息

Annu Rev Med. 2018 Jan 29;69:191-207. doi: 10.1146/annurev-med-061516-121357.

Abstract

The concept of exploiting the specific binding properties of monoclonal antibodies as a mechanism for selective delivery of cytotoxic agents to tumor cells is an attractive solution to the challenge of increasing the therapeutic index of cell-killing agents for treating cancer. All three parts of an antibody-drug conjugate (ADC)-the antibody, the cytotoxic payload, and the linker chemistry that joins them together-as well as the biologic properties of the cell-surface target antigen are important in designing an effective anticancer agent. The approval of brentuximab vedotin in 2011 for treating relapsed Hodgkin's lymphoma and systemic anaplastic large cell lymphoma, and the approval of ado-trastuzumab emtansine in 2013 for treating HER2-positive metastatic breast cancer, have sparked vigorous research in the field, with >65 ADCs currently in clinical evaluation. This review highlights the ADCs that are approved for marketing, in pivotal clinical trials, or in at least phase II clinical development for treating both hematologic malignancies and solid tumors.

摘要

利用单克隆抗体的特异性结合特性作为将细胞毒性药物选择性递送至肿瘤细胞的机制的概念,为提高用于治疗癌症的细胞杀伤剂的治疗指数提供了一个有吸引力的解决方案。抗体药物偶联物(ADC)的三个部分——抗体、细胞毒性有效载荷以及连接它们的连接子化学,以及细胞表面靶抗原的生物学特性,在设计有效的抗癌药物方面都很重要。2011 年,brentuximab vedotin 获批用于治疗复发的霍奇金淋巴瘤和系统性间变性大细胞淋巴瘤,2013 年 ado-trastuzumab emtansine 获批用于治疗 HER2 阳性转移性乳腺癌,这激发了该领域的积极研究,目前有超过 65 种 ADC 正在进行临床评估。这篇综述重点介绍了已批准上市、正在关键性临床试验中或至少处于 II 期临床开发阶段的用于治疗血液系统恶性肿瘤和实体瘤的 ADC。

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