医学
药物开发
临床实习
药品
酪氨酸激酶
癌症研究
机制(生物学)
酪氨酸激酶抑制剂
临床试验
肺癌
药理学
生物信息学
蛋白酪氨酸激酶
免疫学
精密医学
抗体-药物偶联物
细胞
抗体
毒性
嵌合抗原受体
肺
癌症
免疫疗法
抗原
药物发现
靶向治疗
计算生物学
作者
Laura Bonanno,Alberto Ronchi,Loc Carlo Bao,Francesca Pante,Sara Sangiorgi,Giulia Pasello,Stefano Indraccolo,Valentina Guarneri
出处
期刊:Pharmaceutics
[Multidisciplinary Digital Publishing Institute]
日期:2026-07-23
卷期号:18 (8): 905-905
标识
DOI:10.3390/pharmaceutics18080905
摘要
The emergence of antibody-drug conjugates (ADCs) targeting trophoblast cell-surface antigen 2 (TROP2) represents a potential paradigm shift in the treatment of EGFR-mutated non-small cell lung cancer (NSCLC), a setting historically characterized by limited therapeutic options following progression on EGFR tyrosine kinase inhibitors (TKIs). This review examines the biological rationale and clinical challenges underpinning the development of anti-TROP2 ADCs in EGFR-mutated NSCLC. From a mechanistic standpoint, TROP2 occupies a unique and dynamic role in EGFR-mutated NSCLC, providing strong biological rationale for clinical development of anti-TROP2 ADCs in this population. Three TROP2-directed ADCs are currently in clinical development in this setting. Available clinical data in previously treated EGFR-mutated patients are critically reviewed here, focusing on efficacy, toxicity profiles, clinical challenges and potential future perspectives.
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