| Literature DB >> 31761724 |
Ye Yao1, Xiaoya Xu2, Lifeng Yang1, Ji Zhu1, Juefeng Wan1, Lijun Shen1, Fan Xia1, Guoxiang Fu2, Yun Deng3, Mengxue Pan2, Qiang Guo2, Xiaoxue Gao2, Yuanchuang Li2, Xinxin Rao2, Yi Zhou2, Liping Liang1, Yaqi Wang1, Jing Zhang1, Hui Zhang1, Guichao Li1, Lixing Zhang4, Junjie Peng5, Sanjun Cai5, Chen Hu6, Jianjun Gao2, Hans Clevers7, Zhen Zhang8, Guoqiang Hua9.
Abstract
Accumulating evidence indicates that patient-derived organoids (PDOs) can predict drug responses in the clinic, but the ability of PDOs to predict responses to chemoradiation in cancer patients remains an open question. Here we generate a living organoid biobank from patients with locally advanced rectal cancer (LARC) treated with neoadjuvant chemoradiation (NACR) enrolled in a phase III clinical trial. Our co-clinical trial data confirm that rectal cancer organoids (RCOs) closely recapitulate the pathophysiology and genetic changes of corresponding tumors. Chemoradiation responses in patients are highly matched to RCO responses, with 84.43% accuracy, 78.01% sensitivity, and 91.97% specificity. These data imply that PDOs predict LARC patient responses in the clinic and may represent a companion diagnostic tool in rectal cancer treatment.Entities:
Keywords: chemoradiation; clinical response; organoids; predict; rectal cancer
Mesh:
Year: 2019 PMID: 31761724 DOI: 10.1016/j.stem.2019.10.010
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 24.633