Abstract |
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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Authors | Yixuan Hu, Yinxing Zhu, Xiaowei Wei, Cuiju Tang, Wenwen Zhang |
Journal | Drugs of today (Barcelona, Spain : 1998)
(Drugs Today (Barc))
Vol. 58
Issue 10
Pg. 491-507
(Oct 2022)
ISSN: 1699-3993 [Print] Spain |
PMID | 36305543
(Publication Type: Review, Journal Article)
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Copyright | Copyright 2022 Clarivate. |
Chemical References |
- Antibodies, Monoclonal
- Antineoplastic Agents
- ERBB2 protein, human
- Immunoconjugates
- Receptor, ErbB-2
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Topics |
- Humans
- Antibodies, Monoclonal
- Antineoplastic Agents
(therapeutic use)
- Carcinoma, Non-Small-Cell Lung
(drug therapy)
- Immunoconjugates
(therapeutic use)
- Lung Neoplasms
(drug therapy)
- Receptor, ErbB-2
(metabolism)
- Stomach Neoplasms
(drug therapy)
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