diitamab vedotin,一种新的her2导向抗体-药物偶联物,用于胃癌和其他实体肿瘤。

Pub Date : 2022-10-01 DOI:10.1358/dot.2022.58.10.3408812
Yixuan Hu, Yinxing Zhu, Xiaowei Wei, Cuiju Tang, Wenwen Zhang
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引用次数: 3

摘要

抗体-药物偶联物(ADC)是一种细胞毒性药物和抗体的结合,已成为癌症治疗中的一颗冉冉升起的新星。dicitamab vedotin (RC48)是一种靶向人表皮生长因子受体2 (HER2)的新型ADC,目前正在多种恶性肿瘤中进行研究。与传统的her2靶向药物相比,RC48的特点是治疗窗口更宽,对正常组织的毒性更小。在本文中,我们将分析RC48的结构成分和机制。此外,我们还提供了RC48在常见恶性肿瘤中的进展概况,重点介绍了RC48在胃或胃食管结癌中的进展,并简要概述了尿路上皮、乳腺癌和其他癌症(如妇科癌、胆道癌、非小细胞肺癌和子宫肌层浸润性膀胱癌)的进展情况。最后,我们还将讨论RC48未来发展面临的挑战和未来提高疗效的方向。
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Disitamab vedotin, a novel HER2-directed antibody-drug conjugate in gastric cancer and other solid tumors.

Antibody-drug conjugates (ADC), a combination of cytotoxic drugs and antibodies, have emerged as a rising star in cancer therapy. Disitamab vedotin (RC48), a novel ADC targeting human epidermal growth factor receptor 2 (HER2), is currently being explored in a variety of malignancies. Compared with conventional HER2-targeting agents, RC48 is characterized by a wider therapeutic window and less toxicity to normal tissues. In this review, we will analyze the structural elements and mechanisms of RC48. Besides, we provide a landscape on the progression of RC48 in common malignancies, focusing on RC48 in gastric or gastroesophageal junction cancer, and a brief overview of urothelial, breast and other cancers (e.g., gynecological cancer, biliary tract cancer, non-small cell lung cancer and myometrial invasive bladder cancer). Finally, we will also discuss future challenges in the development of RC48 and future directions to improve efficacy.

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