医学
免疫疗法
癌症研究
肿瘤科
小眼畸形相关转录因子
靶向治疗
临床终点
肉瘤
内科学
共刺激
联合疗法
临床试验
临床研究阶段
免疫检查点
免疫系统
黑色素瘤
程序性细胞死亡
存活率
无进展生存期
作者
Yaling Jiang,Nong Lin,Xin Huang,Xiaobo Yan,Meng Liu,Hao Qu,Xiumao Li,Lin Peng,Hui Li,Zhaoming Ye,Binghao Li
出处
期刊:Future Oncology
[Future Medicine]
日期:2026-06-30
卷期号:22 (17): 2047-2053
标识
DOI:10.1080/14796694.2026.2695212
摘要
Clear cell sarcoma (CCS) is an ultra-rare sarcoma with no established standard systemic therapy of proven efficacy. Mesenchymal-epithelial transition factor (MET) overexpression drives CCS progression and serves as a promising therapeutic target. Vebreltinib is a highly selective MET inhibitor with potential therapeutic benefits for CCS. Additionally, given that MET and programmed cell death protein 1 (PD-1) are both downstream molecules of melanocyte transcription factor (MITF), combined MET and PD-1 inhibition may block the MITF pathway more effectively. Moreover, aberrant MET activation indirectly upregulates programmed death ligand 1 (PD-L1), causing immune escape and resistance to PD-1 inhibitors; MET inhibition may potentially reverse this resistance. Here, we describe the rationale and design of VEBrant, a multicenter, phase II study aimed to evaluate the efficacy and safety of vebreltinib combined with PD-1-based immunotherapy in advanced CCS. Thirty patients will be enrolled, with the treatment cohort receiving combination therapy of vebreltinib and PD-1 inhibitor, and a reference cohort receiving physician’s choice therapy or best supportive care. Primary endpoint is Objective Response Rate (ORR) by Simon two-stage design. This study will provide evidence for vebreltinib combined with PD-1-based immunotherapy and improve understanding of advanced CCS management.Clinical trial registration: www.clinicaltrials.gov identifier is NCT07153887.
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