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Background: The desmoplastic histopathological growth pattern (dHGP) of colorectal liver metastases (CRLM) is associated with prolonged survival and favorable anti-angiogenic chemotherapy response. However, reliable preoperative identification of dHGP using MRI remains challenging.
Purpose: To develop a dynamic contrast-enhanced MRI (DCE-MRI)-based model for assessing dHGP probability, facilitating candidate selection for anti-angiogenic neoadjuvant chemotherapy, and prognostic evaluation.
Study Type: Retrospective, dual-center study.
Subjects: 286 patients (114 female; 133 with dHGP) with pathologically confirmed CRLM (≥ 10 mm).
Field Strength/sequence: 3.0 T, T1-weighted imaging using 3D gradient sequence (precontrast, arterial, portal venous and delayed phases).
Assessment: Three abdominal radiologists independently reviewed DCE-MRI features, including peritumoral rim enhancement at different phases for dHGP assessment. Disease-free survival (DFS), overall survival (OS), and treatment response to bevacizumab were also assessed.
Statistical Tests: Univariable and multivariable logistic regression, area under the receiver operating characteristic curve (AUC), DeLong test, Kaplan-Meier analysis, and log-rank test.
Results: Peritumoral rim enhancement on arterial (odds ratio [OR] = 4.65, [95% CI: 2.20-9.84]), portal venous (OR = 7.46, [95% CI: 3.12-17.84]), and delayed phases (OR = 3.55, [95% CI: 1.84-6.88]) was significantly and independently associated with dHGP. A peritumoral rim enhancement-based probability model achieved AUCs of 0.86 (95% CI: 0.81-0.90) and 0.82 (95% CI: 0.70-0.91) for diagnosing dHGP in development and external validation cohorts, respectively. Peritumoral rim enhancement was independently associated with longer survival (DFS: adjusted hazard ratio [HR] = 0.34, [95% CI: 0.25-0.47]; OS: HR = 0.46, [95% CI: 0.34-0.63]) in all patients. Among patients receiving bevacizumab-containing neoadjuvant chemotherapy (n = 90), peritumoral rim enhancement was significantly associated with longer DFS (HR = 0.24, [95% CI: 0.12-0.49]) and OS (HR = 0.24, [95% CI: 0.11-0.50]).
Data Conclusion: Peritumoral rim enhancement on DCE-MRI shows a strong association with dHGP, indicates favorable survival, and may identify candidates for anti-angiogenic chemotherapy.
Evidence Level: 3.
Technical Efficacy: Stage 2.
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http://dx.doi.org/10.1002/jmri.70060 | DOI Listing |
Comput Methods Programs Biomed
November 2025
Laboratory of Computing, Medical Informatics and Biomedical Imaging Technologies, School of Medicine, Aristotle University of Thessaloniki, Greece. Electronic address:
Background: Lung cancer is the leading cause of cancer-related mortality globally. Early detection of high-risk patients for local or distant metastasis is challenging for better monitoring and treatment planning. Machine learning models have been proposed for diagnosis and prediction of metastasis risk.
View Article and Find Full Text PDFJ Magn Reson Imaging
July 2025
Department of Radiology, Shengjing Hospital of China Medical University, Shenyang, Liaoning Province, People's Republic of China.
Background: The desmoplastic histopathological growth pattern (dHGP) of colorectal liver metastases (CRLM) is associated with prolonged survival and favorable anti-angiogenic chemotherapy response. However, reliable preoperative identification of dHGP using MRI remains challenging.
Purpose: To develop a dynamic contrast-enhanced MRI (DCE-MRI)-based model for assessing dHGP probability, facilitating candidate selection for anti-angiogenic neoadjuvant chemotherapy, and prognostic evaluation.
J Mater Chem B
August 2025
Integrative Biomedical Materials and Nanomedicine Lab, Department of Medicine and Life Sciences (MELIS), Pompeu Fabra University, PRBB, Carrer Doctor Aiguader 88, 08003 Barcelona, Spain.
Melanoma is a highly aggressive skin cancer that often develops resistance to chemotherapy, underscoring the need for new treatment strategies. Here we evaluate plasmonic gold nanocapsules (AuNCs) as photoresponsive agents for two-photon luminescence-assisted photothermal therapy in chemoresistant melanoma models. The performance of the AuNCs was assessed in two-dimensional cell cultures, three-dimensional paclitaxel-resistant B16-F10 melanoma spheroids, and a subcutaneous melanoma mouse model under near-infrared excitation.
View Article and Find Full Text PDFNMR Biomed
August 2025
Department of Physics, Oakland University, Rochester, Michigan, USA.
Two preclinical patient-derived orthotopic xenograft (PDOX) models of glioblastoma (GBM) were characterized using measures of tumor physiology. Plasma volume fraction (v), blood-to-tissue forward volumetric transfer constant (K), and interstitial volume fraction (v) were estimated via dynamic contrast-enhanced (DCE) MRI. Tumor blood flow (TBF) was estimated via continuous arterial spin-labeling and apparent diffusion coefficient of water (ADC) via spin-echo diffusion-weighted imaging.
View Article and Find Full Text PDFLiver Cancer
June 2025
Department of Radiology, Kobe University Graduate School of Medicine, Kobe, Japan.
Introduction: Immunotherapy is the first-line treatment for intermediate-advanced stage hepatocellular carcinoma (HCC), although its outcomes vary. This study aimed to identify imaging biomarkers of immunotherapy susceptibility linked to gadoxetic acid-enhanced magnetic resonance imaging (EOB-MRI) and immune phenotypes, particularly immune-excluded phenotypes, with a tumor immune barrier.
Methods: We performed immunohistochemical staining with a CD8 antibody, and samples were classified into immune-inflamed, -intermediate, -excluded, and -ignored phenotypes.