OSCR

NeuroSPFNet: Vision-Language Semantic Prior-Guided Frequency-Enhanced Network for Brain Tumor Segmentation in Multimodal MRI.

Overview

  1. Department of Computer Information Engineering, Kunsan National University, Gunsan 54150, Republic of Korea
Institutions: Kunsan National University (South Korea)
Journal: Sensors (Basel, Switzerland), volume 26, issue 15, article 4963
Dates: received 9 June 2026; accepted 29 July 2026; published online 5 August 2026
Type: Research article · Language: English
License: CC BY
Identifiers: DOI 10.3390/s26154963 · PMID 42590740 · PMCID PMC13468934 · OpenAlex W7172485687
Open access: gold, a free copy (OpenAlex)
Categories: structural MRI / diffusion (modality), human (organism), other condition (population), methods / tools (subfield)
Methods: Connectivity, Preprocessing, Spectral & time-frequency, Machine learning
Keywords: brain tumor segmentation, multimodal MRI, vision–language model, clinical semantic prior, frequency enhancement, boundary-aware segmentation, multimodal medical imaging, deep learning
MeSH: Brain Neoplasms*, Image Processing, Computer-Assisted*, Magnetic Resonance Imaging*, Algorithms, Humans, Multimodal Imaging, Semantics (* major topic)
Topic: Advanced Neural Network Applications (Computer Vision and Pattern Recognition, Computer Science), according to OpenAlex
Citations: not cited yet (Europe PMC); 36 references in the paper

Abstract

Accurate brain tumor segmentation in multimodal magnetic resonance imaging (MRI) scans is essential for quantitative neuro-oncology analysis, treatment planning, and longitudinal disease monitoring. However, automatic delineation remains challenging because glioma subregions exhibit heterogeneous appearance across T1-weighted (T1), contrast-enhanced T1-weighted (T1ce), T2-weighted (T2), and fluid-attenuated inversion recovery (FLAIR) sequences; weak and irregular lesion boundaries; and severe scale variation between edema, tumor core, and enhancing tumor regions. This paper presents NeuroSPFNet, a vision–language semantic prior-guided frequency-enhanced segmentation framework for tumor subregion delineation in multimodal MRI volumes. NeuroSPFNet integrates four complementary components: a Clinical Vision–Language Prior Component (CVLPC) for category-level semantic guidance; a Frequency-Enhanced Boundary Module (FEBM) for boundary-sensitive representation learning; a Multi-Scale Lesion-Dominated Fusion Module (MLDFM) for hierarchical lesion aggregation; and a Lesion-Semantic Boundary Consistency Loss (LSBCL) for jointly constraining region overlap, boundary quality, and semantic alignment. The task-specific contribution lies in the closed coupling of shared BraTS-region semantic prototypes, gated frequency responses, lesion-weighted multiscale features, and semantic-boundary supervision within one volumetric segmentation pipeline. On the Brain Tumor Segmentation (BraTS) 2021 benchmark, NeuroSPFNet achieved Dice scores of 91.94%, 88.84%, and 85.38% for whole tumor, tumor core, and enhancing tumor, respectively, with a mean Dice of 88.72% and a mean 95th-percentile Hausdorff distance (HD95) of 3.58 mm. Ablation studies show distinct effects across subregions and metrics: semantic priors primarily strengthen tumor-core and enhancing-tumor discrimination, whereas frequency and boundary constraints primarily reduce contour error. NeuroSPFNet also attains competitive performance under the current setting, with moderate computational overhead of 42.58 million parameters, 78.60 billion floating-point operations (GFLOPs), and 265 ms per volume.

Reproduced under the paper's license (CC BY), from the paper cited above.

Code

The paper links to its data and to no code of its authors: see the Data section.

Tracing map

A tracing map links a paper to the code its authors published: this paper has none, so it has no map.

Data

Datasets cited

Data Availability Statement

The 1251 labeled BraTS 2021 cases used for model development are available through the official BraTS 2021 Synapse portal (https://www.synapse.org/Synapse:syn25829067/wiki/626944, accessed on 28 July 2026), subject to the benchmark terms and data use agreement. The 219 label-withheld challenge cases were not used to calculate the locally reported metrics.

Reproduced under the paper's license (CC BY), from the paper cited above.

Versions

The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.

Version 1, 27 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 3 authors, 8 keywords, 7 MeSH terms, 1 funder, 17 references.

Cite

This paper

Liu, Y., Shin, S.-Y., & Lee, H.-A. (2026). NeuroSPFNet: Vision-Language Semantic Prior-Guided Frequency-Enhanced Network for Brain Tumor Segmentation in Multimodal MRI. Sensors (Basel, Switzerland), 26(15), 4963. https://doi.org/10.3390/s26154963

BibTeX

@article{liu2026neurospfnet,
author = {Liu, Yantong and Shin, Seong-Yoon and Lee, Hyun-Ae},
title = {{NeuroSPFNet: Vision-Language Semantic Prior-Guided Frequency-Enhanced Network for Brain Tumor Segmentation in Multimodal MRI}},
journal = {Sensors (Basel, Switzerland)},
year = {2026},
month = aug,
volume = {26},
number = {15},
pages = {4963},
publisher = {Multidisciplinary Digital Publishing Institute (MDPI)},
issn = {1424-8220},
doi = {10.3390/s26154963},
url = {https://doi.org/10.3390/s26154963},
pmid = {42590740},
pmcid = {PMC13468934}
}

RIS

TY - JOUR
AU - Liu, Yantong
AU - Shin, Seong-Yoon
AU - Lee, Hyun-Ae
TI - NeuroSPFNet: Vision-Language Semantic Prior-Guided Frequency-Enhanced Network for Brain Tumor Segmentation in Multimodal MRI
T2 - Sensors (Basel, Switzerland)
J2 - Sensors (Basel)
PY - 2026
DA - 2026/08/05
VL - 26
IS - 15
SP - 4963
SN - 1424-8220
PB - Multidisciplinary Digital Publishing Institute (MDPI)
DO - 10.3390/s26154963
UR - https://doi.org/10.3390/s26154963
LA - en
ER -

CSL-JSON

{
"id": "10.3390/s26154963",
"type": "article-journal",
"title": "NeuroSPFNet: Vision-Language Semantic Prior-Guided Frequency-Enhanced Network for Brain Tumor Segmentation in Multimodal MRI",
"container-title": "Sensors (Basel, Switzerland)",
"author": [
{
"family": "Liu",
"given": "Yantong"
},
{
"family": "Shin",
"given": "Seong-Yoon"
},
{
"family": "Lee",
"given": "Hyun-Ae"
}
],
"container-title-short": "Sensors (Basel)",
"volume": "26",
"issue": "15",
"page": "4963",
"DOI": "10.3390/s26154963",
"PMID": "42590740",
"PMCID": "PMC13468934",
"ISSN": "1424-8220",
"publisher": "Multidisciplinary Digital Publishing Institute (MDPI)",
"URL": "https://doi.org/10.3390/s26154963",
"language": "en",
"issued": {
"date-parts": [
[
2026,
8,
5
]
]
}
}

Similar papers

The papers with a page that share the most with this one: the tools found in their code, their categories, datasets, cited references and authors, the rarest counting most.

[1] doi:10.3390/diagnostics16172806
Brain Tumor Segmentation and Grading on MRI Using Deep Learning: A Systematic Literature Review and Benchmark-Driven Comparative Analysis.
Journal: Diagnostics (Basel, Switzerland)
In common: methods / tools, structural MRI / diffusion, other condition, 8 references
[2] doi:10.3390/s25061838
Advancing Precision: A Comprehensive Review of MRI Segmentation Datasets from BraTS Challenges (2012-2025).
Journal: Sensors (Basel, Switzerland)
In common: synapse.org/synapse:syn25829067/wiki, methods / tools, structural MRI / diffusion, other condition, 2 references
[3] doi:10.21037/qims-2026-0792 [code]
An nnU-Net-based framework with adaptive feature representation for 3D brain tumor segmentation.
Journal: Quantitative imaging in medicine and surgery
In common: methods / tools, structural MRI / diffusion, other condition, 5 references
[4] doi:10.3389/fninf.2022.1056068 [code]
2.5D and 3D segmentation of brain metastases with deep learning on multinational MRI data.
Journal: Frontiers in neuroinformatics
In common: methods / tools, structural MRI / diffusion, other condition, 5 references
[5] doi:10.2174/0115734056344235241217155930 [code]
Advanced CNN Architecture for Brain Tumor Segmentation and Classification using BraTS-GOAT 2024 Dataset.
Journal: Current medical imaging
In common: methods / tools, structural MRI / diffusion, other condition, 5 references
[6] doi:10.1016/j.dib.2025.111287
GBM-Reservoir: Brain tumor (Glioblastoma Multiforme) MRI dataset collection with ground truth segmentation masks.
Journal: Data in brief
In common: methods / tools, structural MRI / diffusion, other condition, 5 references
[7] doi:10.3389/fnins.2022.911065 [code]
Overall Survival Prediction of Glioma Patients With Multiregional Radiomics.
Journal: Frontiers in neuroscience
In common: structural MRI / diffusion, other condition, 5 references
[8] doi:10.1002/hbm.70317 [code]
Towards an Informed Choice of Diffusion MRI Image Contrasts for Cerebellar Segmentation.
Journal: Human brain mapping
In common: synapse.org/synapse:syn25829067/wiki, methods / tools, structural MRI / diffusion
[9] doi:10.3390/s23073420 [code]
High-Resolution Swin Transformer for Automatic Medical Image Segmentation.
Journal: Sensors (Basel, Switzerland)
In common: methods / tools, 5 references
[10] doi:10.1038/s41698-025-01173-4
Unsupervised generative AI for enhancing brain tumor segmentation in multi-center, incomplete real-world data scenarios.
Journal: NPJ precision oncology
In common: methods / tools, structural MRI / diffusion, other condition, 4 references

Contribute

The authors of this paper can claim it, correct its record and validate its tracing map, and the maintainers of its code (its owner, or a public member of its organization) correct what it says of their repository; anyone signed in can ask for its removal. Every request goes to OSCR's own machine, which answers it; your account page follows them.

Sign in with ORCID to claim this paper as one of its authors, correct its record or validate its tracing map: when the paper's metadata lists your ORCID iD, you are recognized at once. Maintainers of its code: sign in with GitHub, then claim the repository on your account page.

Request its removal

To ask OSCR to remove this record, the copies of its authors' scripts or its tracing map, use the removal request page: signed in, you say who you are, what to remove and why, then review and confirm the request. Published rules decide every request (how).

Discussion, reproductions, activity

Discussion: code errors and mismatches between the code and the paper about this paper and its code, from readers and its authors, beside the paper and its tracing map.

Reproductions: reports from readers who ran the authors' code and did not get the paper's result, what they ran, with which environment, commit and data.

Activity: what happens around this paper: new versions of its record, its map's validation, discussions and reproductions. It opens with sign-in.