Evidence map›Paper›PMID 42434230›Full record

ArticleJournal of gastrointestinal oncology2026

Deep learning model based on MRI-derived microvascular network simulation parameters for noninvasive assessment of lymphovascular invasion in rectal cancer patients.

Yue Di, Xiaofeng Jin, Lei Han, Qin Lu, Tingting Han

Abstract read
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Article in Journal of gastrointestinal oncology, 2026. 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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1 · What the graph read from it

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Yue DiDepartment of Radiology, No. 904 Hospital of Joint Logistics Support Force of PLA, Wuxi, China.
Xiaofeng JinDepartment of Radiology, No. 904 Hospital of Joint Logistics Support Force of PLA, Wuxi, China.
Lei HanDepartment of Medical Imaging, The Affiliated Huai'an Hospital of Xuzhou Medical University, Huai'an, China.
Qin LuDepartment of Medical Ultrasonography, The Affiliated Huai'an Hospital of Xuzhou Medical University, Huaian, China.
Tingting HanDepartment of Medical Imaging, The Affiliated Huai'an Hospital of Xuzhou Medical University, Huai'an, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Accurate preoperative assessment of lymphovascular invasion (LVI) in patients with rectal cancer (RC) is important for guiding postoperative management. This study aimed to develop and validate a deep learning model based on magnetic resonance imaging (MRI)-derived microvascular network simulation parameters for the preoperative assessment of LVI in RC patients. Methods: A total of 453 patients with pathologically confirmed rectal adenocarcinoma from two medical centers were retrospectively enrolled. All patients underwent multi-b-value diffusion-weighted imaging (DWI) before surgery. First, a steady-state Navier-Stokes hemodynamic model of the tumor microvascular network was constructed based on the multi-b-value DWI images. Subsequently, voxel-wise least squares fitting was performed to match the DWI signals with the dictionary, enabling the inversion and generation of spatial parametric maps for mean flow velocity (V-m), velocity standard deviation (V-s), and angiogenic branching index (ANB). These parametric maps were then input into a Vision Transformer (ViT) network to extract deep features from each modality. A cross-attention fusion module was designed to capture spatial interactions among the parametric maps and construct a multiparametric fusion model. The model's performance was comprehensively evaluated using the area under the curve (AUC), calibration curves, and decision curve analysis (DCA). Results: The multiparametric fusion model achieved favorable performance, with AUCs of 0.901 [95% confidence interval (CI): 0.808-0.993] and 0.863 (95% CI: 0.800-0.926) in the internal and external validation cohorts, respectively. DCA demonstrated that within the threshold range of 0.2-0.8, the fusion model provided substantially greater clinical net benefit than the individual parameter models. Gradient-weighted Class Activation Mapping (Grad-CAM) visualization revealed that the model's attention was primarily focused on the invasive front of the tumor and regions with high peritumoral vascular density, providing supportive visual evidence and suggesting potential biological relevance. Conclusions: The deep learning model based on MRI-simulated microvascular network parameters provides a promising and noninvasive approach for the preoperative assessment of LVI status in RC patients. The model demonstrated encouraging performance in both internal and external validation cohorts. However, further prospective and multicenter validation is required before clinical application.

Indexed as

deep learninglymphovascular invasion (LVI)magnetic resonance imaging (MRI)microvascular network simulationRectal cancer (RC)

Identifiers

PMID42434230
PMCPMC13350638

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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.