前列腺癌
癌症
癌症研究
体外
体内
前列腺
癌细胞
旁观者效应
流式细胞术
T细胞
细胞
医学
临床试验
生物
单克隆抗体
前列腺特异性抗原
治疗方法
肿瘤科
渗透(HVAC)
神经内分泌分化
转录组
免疫学
内科学
作者
Sheng‐Yu Ku,Nishat Manzar,Maria Mica Garcia,Min Jin Kim,David J. Einstein,Steven P. Balk,Yasutaka Yamada,Himisha Beltran
标识
DOI:10.1158/1535-7163.mct-25-0453
摘要
Neuroendocrine prostate cancer (NEPC) is an aggressive variant of prostate cancer with limited therapeutic options. Delta-like ligand 3 (DLL3) is a cell-surface protein and therapeutic target expressed in the vast majority of NEPC tumors. The DLL3-targeted T cell-activating construct MK-6070 (formerly called HPN328) binds to both DLL3 on tumor cells and CD3 on T cells, as well as serum albumin to extend half-life. A phase I/II trial of MK-6070 is currently underway, which includes an NEPC cohort (NCT04471727). In this study, we report the preclinical activity of MK-6070 in prostate cancer models, showing high specificity and antitumor activity in DLL3-expressing NEPC models both in vitro and in vivo, with T-cell activation and tumor infiltration of T cells after treatment. MK-6070 also demonstrates antitumor activity in mixed tumors, affecting DLL3-negative prostate cancer cells after engagement with surrounding DLL3-expressing tumor cells, supporting a potential bystander effect. Overall, these data demonstrate the promising activity of MK-6070 in NEPC preclinical models including heterogeneous tumors, supporting the clinical development of MK-6070.
科研通智能强力驱动
Strongly Powered by AbleSci AI