生物
肺癌
个性化医疗
间质细胞
癌症研究
肿瘤科
药品
免疫系统
精密医学
免疫疗法
临床试验
癌症
生物信息学
免疫学
内科学
遗传学
药理学
医学
作者
Shenyi Yin,Ying Yu,Nan Wu,Minglei Zhuo,Yanmin Wang,Yanjie Niu,Yiqian Ni,Fang Hu,Cuiming Ding,Huan Liu,Xinghua Cheng,Jin Peng,Juan Li,Yang He,Jiaxin Li,Junyi Wang,Hanshuo Zhang,Xiaoyu Zhai,Bing Liu,Yaqi Wang
出处
期刊:Cell Stem Cell
[Elsevier BV]
日期:2024-04-08
卷期号:31 (5): 717-733.e8
被引量:9
标识
DOI:10.1016/j.stem.2024.03.008
摘要
Many patient-derived tumor models have emerged recently. However, their potential to guide personalized drug selection remains unclear. Here, we report patient-derived tumor-like cell clusters (PTCs) for non-small cell lung cancer (NSCLC), capable of conducting 100–5,000 drug tests within 10 days. We have established 283 PTC models with an 81% success rate. PTCs contain primary tumor epithelium self-assembled with endogenous stromal and immune cells and show a high degree of similarity to the original tumors in phenotypic and genotypic features. Utilizing standardized culture and drug-response assessment protocols, PTC drug-testing assays reveal 89% overall consistency in prospectively predicting clinical outcomes, with 98.1% accuracy distinguishing complete/partial response from progressive disease. Notably, PTCs enable accurate prediction of clinical outcomes for patients undergoing anti-PD1 therapy by combining cell viability and IFN-γ value assessments. These findings suggest that PTCs could serve as a valuable preclinical model for personalized medicine and basic research in NSCLC.
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