Development and validation of a radiopathomics model to predict pathological complete response to neoadjuvant chemoradiotherapy in locally advanced rectal cancer: a multicentre observational study
文献类型:期刊论文
作者 | Feng, Lili1,14; Liu, Zhenyu13; Li, Chaofeng12; Li, Zhenhui10; Lou, Xiaoying17; Shao, Lizhi9,13; Wang, Yunlong1,14; Huang, Yan17; Chen, Haiyang1; Pang, Xiaolin1 |
刊名 | LANCET DIGITAL HEALTH |
出版日期 | 2022 |
卷号 | 4期号:1页码:E8-E17 |
通讯作者 | Tian, Jie(jie.tian@ia.ac.cn) ; Wan, Xiangbo(wanxbo@mail.sysu.edu.cn) |
英文摘要 | Background Accurate prediction of tumour response to neoadjuvant chemoradiotherapy enables personalised perioperative therapy for locally advanced rectal cancer. We aimed to develop and validate an artificial intelligence radiopathomics integrated model to predict pathological complete response in patients with locally advanced rectal cancer using pretreatment MRI and haematoxylin and eosin (H&E)-stained biopsy slides. Methods In this multicentre observational study, eligible participants who had undergone neoadjuvant chemoradiotherapy followed by radical surgery were recruited, with their pretreatment pelvic MRI (T2-weighted imaging, contrast-enhanced T1-weighted imaging, and diffusion-weighted imaging) and whole slide images of H&E-stained biopsy sections collected for annotation and feature extraction. The RAdioPathomics Integrated preDiction System (RAPIDS) was constructed by machine learning on the basis of three feature sets associated with pathological complete response: radiomics MRI features, pathomics nucleus features, and pathomics microenvironment features from a retrospective training cohort. The accuracy of RAPIDS for the prediction of pathological complete response in locally advanced rectal cancer was verified in two retrospective external validation cohorts and further validated in a multicentre, prospective observational study (ClinicalTrials.gov, NCT04271657). Model performances were evaluated using area under the curve (AUC), sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV). Findings Between Sept 25, 2009, and Nov 3, 2017, 303 patients were retrospectively recruited in the training cohort, 480 in validation cohort 1, and 150 in validation cohort 2; 100 eligible patients were enrolled in the prospective study between Jan 10 and June 10, 2020. RAPIDS had favourable accuracy for the prediction of pathological complete response in the training cohort (AUC 0.868 [95% CI 0.825-0.912]), and in validation cohort 1 (0.860 [0.828-0.892]) and validation cohort 2 (0.872 [0.810-0.934]). In the prospective validation study, RAPIDS had an AUC of 0.812 (95% CI 0-717-0.907), sensitivity of 0.888 (0.728-0.999), specificity of 0.740 (0.593-0.886), NPV of 0.929 (0.862-0.995), and PPV of 0.512 (0.313-0.710). RAPIDS also significantly outperformed single-modality prediction models (AUC 0.630 [0.507-0.754] for the pathomics microenvironment model, 0.716 [0.580-0-852] for the radiomics MRI model, and 0.733 [0.620-0.845] for the pathomics nucleus model; all p<0.0001). Interpretation RAPIDS was able to predict pathological complete response to neoadjuvant chemoradiotherapy based on pretreatment radiopathomics images with high accuracy and robustness and could therefore provide a novel tool to assist in individualised management of locally advanced rectal cancer. Copyright (C) 2021 The Author(s). Published by Elsevier Ltd. |
WOS关键词 | ARTIFICIAL-INTELLIGENCE ; RADIOMICS ; IMAGES |
资助项目 | National Natural Science Foundation of China ; Youth Innovation Promotion Association of the Chinese Academy of Sciences |
WOS研究方向 | Medical Informatics ; General & Internal Medicine |
语种 | 英语 |
出版者 | ELSEVIER |
WOS记录号 | WOS:000736243900006 |
资助机构 | National Natural Science Foundation of China ; Youth Innovation Promotion Association of the Chinese Academy of Sciences |
源URL | [http://ir.ia.ac.cn/handle/173211/47103] |
专题 | 自动化研究所_中国科学院分子影像重点实验室 |
通讯作者 | Tian, Jie; Wan, Xiangbo |
作者单位 | 1.Sun Yat Sen Univ, Affiliated Hosp 6, Dept Radiat Oncol, Guangzhou 510000, Peoples R China 2.Univ Michigan, Canc Ctr, Ann Arbor, MI 48109 USA 3.Univ Michigan, Dept Radiat Oncol, Ann Arbor, MI 48109 USA 4.Asia Univ, Dept Biotechnol, Taichung, Taiwan 5.China Med Univ, Res Ctr Canc Biol & Mol Med, Taichung, Taiwan 6.China Med Univ, Grad Inst Biomed Sci, Taichung, Taiwan 7.Univ Texas MD Anderson Canc Ctr, Dept Mol & Cellular Oncol, Houston, TX 77030 USA 8.Southern Med Univ, Nanfang Hosp, Dept Radiat Oncol, Guangzhou, Peoples R China 9.Southeast Univ, Sch Comp Sci & Engn, Nanjing, Peoples R China 10.Kunming Med Univ, Yunnan Canc Hosp, Dept Radiol, Affiliated Hosp 3, Kunming, Yunnan, Peoples R China |
推荐引用方式 GB/T 7714 | Feng, Lili,Liu, Zhenyu,Li, Chaofeng,et al. Development and validation of a radiopathomics model to predict pathological complete response to neoadjuvant chemoradiotherapy in locally advanced rectal cancer: a multicentre observational study[J]. LANCET DIGITAL HEALTH,2022,4(1):E8-E17. |
APA | Feng, Lili.,Liu, Zhenyu.,Li, Chaofeng.,Li, Zhenhui.,Lou, Xiaoying.,...&Wan, Xiangbo.(2022).Development and validation of a radiopathomics model to predict pathological complete response to neoadjuvant chemoradiotherapy in locally advanced rectal cancer: a multicentre observational study.LANCET DIGITAL HEALTH,4(1),E8-E17. |
MLA | Feng, Lili,et al."Development and validation of a radiopathomics model to predict pathological complete response to neoadjuvant chemoradiotherapy in locally advanced rectal cancer: a multicentre observational study".LANCET DIGITAL HEALTH 4.1(2022):E8-E17. |
入库方式: OAI收割
来源:自动化研究所
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