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ArticleEuropean radiology2026

MRI-based habitat analysis for pathologic response prediction after neoadjuvant chemoradiotherapy in rectal cancer: a multicenter study.

Qiaoling Chen, Qianwen Zhang, Zhihui Li, Shaoting Zhang, Yuwei Xia, Hao Wang, Yong Lu, Anqi Zheng, Chengwei Shao, Fu Shen

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in European radiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

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6citing papers in PubMed
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6 citing papers in PubMed.

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5 · Who and what money

Authors and funding

10 authors.

Qiaoling Chen *Department of Radiology, Changhai Hospital, Shanghai, China.
Qianwen Zhang *Department of Radiology, Changhai Hospital, Shanghai, China.
Zhihui LiDepartment of Radiology, Ruijin Hospital Luwan Branch, Shanghai Jiaotong University School of Medicine, Shanghai, China.
Shaoting ZhangDepartment of Radiology, Shandong Cancer Hospital and Institute, Jinan, China.
Yuwei XiaShanghai United Imaging Intelligence, Shanghai, China.
Hao WangDepartment of Colorectal Surgery, Changhai Hospital, Shanghai, China.
Yong LuShanghai Jiaotong University School of Medicine, Shanghai, China.
Anqi ZhengDepartment of Radiology, Changhai Hospital, Shanghai, China.
Chengwei ShaoDepartment of Radiology, Changhai Hospital, Shanghai, China.
Fu ShenDepartment of Radiology, Changhai Hospital, Shanghai, China. ssff_53@163.com.ORCID http://orcid.org/0000-0001-8596-9563

Funding

Second Military Medical University 2023QN049
6 · The paper itself

Abstract

objectivesTo investigate MRI-based habitat analysis for its value in predicting pathologic response following neoadjuvant chemoradiotherapy (nCRT) in rectal cancer (RC) patients. MATERIALS AND

methods1021 RC patients in three hospitals were divided into the training and test sets (n = 319), the internal validation set (n = 317), and external validation sets 1 (n = 158) and 2 (n = 227). Deep learning was performed to automatically segment the entire lesion on high-resolution MRI. Simple linear iterative clustering was used to divide each tumor into subregions, from which radiomics features were extracted. The optimal number of clusters reflecting the diversity of the tumor ecosystem was determined. Finally, four models were developed: clinical, intratumoral heterogeneity (ITH)-based, radiomics, and fusion models. The performance of these models was evaluated. The impact of nCRT on disease-free survival (DFS) was further analyzed.

resultsThe Delong test revealed the fusion model (AUCs of 0.867, 0.851, 0.852, and 0.818 in the four cohorts, respectively), the radiomics model (0.831, 0.694, 0.753, and 0.705, respectively), and the ITH model (0.790, 0.786, 0.759, and 0.722, respectively) were all superior to the clinical model (0.790, 0.605, 0.735, and 0.704, respectively). However, no significant differences were detected between the fusion and ITH models. Patients stratified using the fusion model showed significant differences in DFS between the good and poor response groups (all p < 0.05 in the four sets).

conclusionThe fusion model combining clinical factors, radiomics features, and ITH features may help predict pathologic response in RC cases receiving nCRT. KEY POINTS: Question Identifying rectal cancer (RC) patients likely to benefit from neoadjuvant chemoradiotherapy (nCRT) before treatment is crucial. Findings The fusion model shows the best performance in predicting response after neoadjuvant chemoradiotherapy. Clinical relevance The fusion model integrates clinical characteristics, radiomics features, and intratumoral heterogeneity (ITH)features, which can be applied for the prediction of response to nCRT in RC patients, offering potential benefits in terms of personalized treatment strategies.

Indexed as

Magnetic Resonance ImagingNeoadjuvant TherapyRectal NeoplasmsAdultAgedChemoradiotherapyDeep LearningFemaleHumansMaleMiddle AgedRetrospective StudiesTreatment OutcomeDeep learningHabitatMagnetic resonance imagingPathologic responseRectal cancer

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.