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用于癌症治疗的药物偶联物的过去、现在与未来。

Past, present and future of drug conjugates for cancer therapy.

作者信息

Cazzamalli S, Puca E, Neri D

机构信息

R&D Department, Philochem AG, Otelfingen, Switzerland.

Department of Chemistry and Applied Biosciences, Swiss Federal Institute of Technology, Zurich, Switzerland.

出版信息

Nat Cancer. 2025 Sep 11. doi: 10.1038/s43018-025-01042-w.

Abstract

Drug conjugates have emerged as promising tumor-targeted cytotoxics with an improved therapeutic index compared to classical chemotherapeutics. Although traditionally based on antibody ligands, high-throughput screening methods, such as peptide display and DNA-encoded chemical libraries, have enabled the isolation of ultra-high-affinity small ligands and the generation of drug conjugates with better tumor-targeting performance. This Perspective examines the history, major clinical milestones and future of drug conjugates for cancer treatment. We also discuss a new wave of combination modalities, linker strategies, and the development of conjugates based on large and small delivery vehicles.

摘要

与传统化疗药物相比,药物偶联物已成为一种有前景的肿瘤靶向细胞毒素,具有更高的治疗指数。尽管传统上基于抗体配体,但高通量筛选方法,如肽展示和DNA编码化学文库,已能够分离出超高亲和力的小配体,并生成具有更好肿瘤靶向性能的药物偶联物。本观点文章探讨了用于癌症治疗的药物偶联物的历史、主要临床里程碑及未来发展。我们还讨论了新一轮的联合治疗模式、连接子策略以及基于大小不同递送载体的偶联物开发。

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