Evidence map›Paper›PMID 41409246›Full record

ArticleFrontiers in oncology2025

Multiparametric-MRI habitat radiomics analysis for discriminating pathological types of brain metastases.

Jinling Zhu, Xin Xie, Jixuan Deng, Ruizhe Xu, Li Zou, Ye Tian, Wu Cai, Bo Zhang

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Article in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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8 authors.

Jinling Zhu *Department of Radiology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Xin Xie *Department of Radiology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Jixuan DengDepartment of Radiology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Ruizhe XuDepartment of Radiotherapy & Oncology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Li ZouDepartment of Radiotherapy & Oncology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Ye TianDepartment of Radiotherapy & Oncology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Wu CaiDepartment of Radiology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Bo ZhangDepartment of Radiology, The Second Affiliated Hospital of Soochow University, Suzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Early identification of the primary tumor types in brain metastases (BMs) is crucial for developing effective treatment strategies. This study aimed to evaluate the potential of multiparametric MRI (mpMRI)-based habitat radiomics analysis in differentiating the pathological types of BMs. Materials and methods: Pre-treatment MR images from 328 BMs patients at a single center were retrospectively collected and randomly divided into a training set (229 cases) and a test set (99 cases). Tumor regions were manually segmented on contrast-enhanced T1-weighted images (CE-T1WI), and the K-means clustering algorithm was employed to classify the tumor into four distinct sub-regions. Radiomics features were extracted separately from each sub-region to construct the habitat model. The resulting habitat model was compared alongside a traditional whole-tumor radiomics model, a clinical model, and a combined model (integrating habitat and clinical variables). Model performance was evaluated by the area under the receiver operating characteristic curve (AUC), as well as accuracy. Results: The combined model achieved the highest overall performance (training AUC: 0.992, accuracy: 0.952; test AUC: 0.939, accuracy: 0.845), outperforming the habitat model (training AUC: 0.965, accuracy: 0.876; test AUC: 0.888, accuracy: 0.835), traditional radiomics model (training AUC: 0.984, accuracy: 0.866; test AUC: 0.884, accuracy: 0.754), and clinical model (training AUC: 0.788, accuracy: 0.731; test AUC: 0.716, accuracy: 0.653). However, class-specific evaluation revealed substantial performance variation, with F1-scores of 0.874 for lung cancer BMs, but only 0.333 and 0.200 for breast and gastrointestinal cancer BMs, respectively. Conclusions: This study demonstrates that while habitat radiomics shows potential for classifying BMs, its current performance is constrained by class imbalance and scanner heterogeneity. Consequently, our primary contribution lies in providing a critical baseline and a clear direction, prioritizing data-centric solutions as the essential next step for the field.

Indexed as

brain metastasesbreast cancergastrointestinal cancerhabitat radiomicslung cancermagnetic resonance imaging

Identifiers

PMID41409246
PMCPMC12705402

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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.