Updated clinical evidence and molecular features of antibody-drug conjugates for advanced urothelial carcinoma

被引:0
作者
Wang, Ching-Yun [1 ]
Teng, Pai-Chi [2 ,3 ]
Hong, Jian-Hua [3 ,4 ]
机构
[1] Taichung Vet Gen Hosp, Dept Med Educ, Taichung, Taiwan
[2] Fu Jen Catholic Univ, Cardinal Tien Hosp, Dept Surg, Div Urol, New Taipei, Taiwan
[3] Natl Taiwan Univ, Natl Taiwan Univ Hosp, Coll Med, Dept Urol, 1 Changde St, Taipei 10048, Taiwan
[4] Natl Taiwan Univ, Dept Biomed Engn, Taipei, Taiwan
关键词
antibody-drug conjugates; chemotherapy; immunotherapy; urothelial carcinoma; ENFORTUMAB VEDOTIN; BLADDER-CANCER; PROSTATE-CANCER; OPEN-LABEL; TROP-2; NECTIN-4; TRIAL; GENE; 1ST-IN-HUMAN; EXPRESSION;
D O I
10.1097/us9.0000000000000020
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Platinum-based chemotherapy and immunotherapy are the primary systemic treatments for patients with advanced urothelial carcinoma (UC). However, the efficacy of these systemic therapies has yet to be optimized. Antibody-drug conjugates (ADCs), which combine the specificity of monoclonal antibodies with the cytotoxic potency of small-molecule drugs, have emerged as a promising new class of targeted therapies for UC. Currently, the Food and Drug Administration has approved 2 ADCs, namely Padcev and Trodelvy, for the treatment of advanced UC. This review provides an overview of the clinical evidence supporting the use of ADCs in patients with UC and summarizes the molecular features underlying these ADCs, which could be essential for understanding resistance mechanisms and minimizing treatment-related adverse events.
引用
收藏
页码:103 / 111
页数:9
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