Topology-Guided Biomechanical Profiling: A White-Box Framework for Opportunistic Screening of Spinal Instability on Routine CT

Fuente: arXiv
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Autori principali: Ye, Zanting, Wu, Xuanbin, Zhong, Guoqing, Liu, Shengyuan, Liu, Jiashuai, Song, Ge, Wang, Zhisong, Hao, Jing, Niu, Xiaolong, Zheng, Yefeng, Zhang, Yu, Lu, Lijun
Natura: Preprint
Pubblicazione: 2026
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author Ye, Zanting
Wu, Xuanbin
Zhong, Guoqing
Liu, Shengyuan
Liu, Jiashuai
Song, Ge
Wang, Zhisong
Hao, Jing
Niu, Xiaolong
Zheng, Yefeng
Zhang, Yu
Lu, Lijun
author_facet Ye, Zanting
Wu, Xuanbin
Zhong, Guoqing
Liu, Shengyuan
Liu, Jiashuai
Song, Ge
Wang, Zhisong
Hao, Jing
Niu, Xiaolong
Zheng, Yefeng
Zhang, Yu
Lu, Lijun
contents Routine oncologic computed tomography (CT) presents an ideal opportunity for screening spinal instability, yet prophylactic stabilization windows are frequently missed due to the complex geometric reasoning required by the Spinal Instability Neoplastic Score (SINS). Automating SINS is fundamentally hindered by metastatic osteolysis, which induces topological ambiguity that confounds standard segmentation and black-box AI. We propose Topology-Guided Biomechanical Profiling (TGBP), an auditable white-box framework decoupling anatomical perception from structural reasoning. TGBP anchors SINS assessment on two deterministic geometric innovations: (i) canal-referenced partitioning to resolve posterolateral boundary ambiguity, and (ii) context-aware morphometric normalization via covariance-based oriented bounding boxes (OBB) to quantify vertebral collapse. Integrated with auxiliary radiomic and large language model (LLM) modules, TGBP provides an end-to-end, interpretable SINS evaluation. Validated on a multi-center, multi-cancer cohort ($N=482$), TGBP achieved 90.2\% accuracy in 3-tier stability triage. In a blinded reader study ($N=30$), TGBP significantly outperformed medical oncologists on complex structural features ($κ=0.857$ vs.\ $0.570$) and prevented compounding errors in Total Score estimation ($κ=0.625$ vs.\ $0.207$), democratizing expert-level opportunistic screening.
format Preprint
id arxiv_https___arxiv_org_abs_2603_16963
institution arXiv
publishDate 2026
record_format arxiv
spellingShingle Topology-Guided Biomechanical Profiling: A White-Box Framework for Opportunistic Screening of Spinal Instability on Routine CT
Ye, Zanting
Wu, Xuanbin
Zhong, Guoqing
Liu, Shengyuan
Liu, Jiashuai
Song, Ge
Wang, Zhisong
Hao, Jing
Niu, Xiaolong
Zheng, Yefeng
Zhang, Yu
Lu, Lijun
Quantitative Methods
Computer Vision and Pattern Recognition
Routine oncologic computed tomography (CT) presents an ideal opportunity for screening spinal instability, yet prophylactic stabilization windows are frequently missed due to the complex geometric reasoning required by the Spinal Instability Neoplastic Score (SINS). Automating SINS is fundamentally hindered by metastatic osteolysis, which induces topological ambiguity that confounds standard segmentation and black-box AI. We propose Topology-Guided Biomechanical Profiling (TGBP), an auditable white-box framework decoupling anatomical perception from structural reasoning. TGBP anchors SINS assessment on two deterministic geometric innovations: (i) canal-referenced partitioning to resolve posterolateral boundary ambiguity, and (ii) context-aware morphometric normalization via covariance-based oriented bounding boxes (OBB) to quantify vertebral collapse. Integrated with auxiliary radiomic and large language model (LLM) modules, TGBP provides an end-to-end, interpretable SINS evaluation. Validated on a multi-center, multi-cancer cohort ($N=482$), TGBP achieved 90.2\% accuracy in 3-tier stability triage. In a blinded reader study ($N=30$), TGBP significantly outperformed medical oncologists on complex structural features ($κ=0.857$ vs.\ $0.570$) and prevented compounding errors in Total Score estimation ($κ=0.625$ vs.\ $0.207$), democratizing expert-level opportunistic screening.
title Topology-Guided Biomechanical Profiling: A White-Box Framework for Opportunistic Screening of Spinal Instability on Routine CT
topic Quantitative Methods
Computer Vision and Pattern Recognition
url https://arxiv.org/abs/2603.16963