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MRI radiomics independent of clinical baseline characteristics and neoadjuvant treatment modalities predicts response to neoadjuvant therapy in rectal cancer

Authors :
Maxiaowei Song
Shuai Li
Hongzhi Wang
Ke Hu
Fengwei Wang
Huajing Teng
Zhi Wang
Jin Liu
Angela Y. Jia
Yong Cai
Yongheng Li
Xianggao Zhu
Jianhao Geng
Yangzi Zhang
XiangBo Wan
Weihu Wang
Source :
British journal of cancer. 127(2)
Publication Year :
2021

Abstract

Background To analyse the performance of multicentre pre-treatment MRI-based radiomics (MBR) signatures combined with clinical baseline characteristics and neoadjuvant treatment modalities to predict complete response to neoadjuvant (chemo)radiotherapy in locally advanced rectal cancer (LARC). Methods Baseline MRI and clinical characteristics with neoadjuvant treatment modalities at four centres were collected. Decision tree, support vector machine and five-fold cross-validation were applied for two non-imaging and three radiomics-based models’ development and validation. Results We finally included 674 patients. Pre-treatment CEA, T stage, and histologic grade were selected to generate two non-imaging models: C model (clinical baseline characteristics alone) and CT model (clinical baseline characteristics combining neoadjuvant treatment modalities). The prediction performance of both non-imaging models were poor. The MBR signatures comprising 30 selected radiomics features, the MBR signatures combining clinical baseline characteristics (CMBR), and the CMBR incorporating neoadjuvant treatment modalities (CTMBR) all showed good discrimination with mean AUCs of 0.7835, 0.7871 and 0.7916 in validation sets, respectively. The three radiomics-based models had insignificant discrimination in performance. Conclusions The performance of the radiomics-based models were superior to the non-imaging models. MBR signatures seemed to reflect LARC’s true nature more accurately than clinical parameters and helped identify patients who can undergo organ preservation strategies.

Details

ISSN :
15321827
Volume :
127
Issue :
2
Database :
OpenAIRE
Journal :
British journal of cancer
Accession number :
edsair.doi.dedup.....2f6ce9e1be4b6642a682058a9ceca89c