Evidence map›Paper›PMID 41613541›Full record

ArticleFrontiers in oncology2025

Value of intra- and peritumoral ultrasound radiomics for predicting axillary lymph node burden in breast cancer.

Mo-Han Hao, Fan Zhang, Cong Zhang, Naijing Shi, Weina Mu

Abstract read
In one paragraph

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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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Mo-Han HaoDepartment of Ultrasound Medicine, Baoding First Central Hospital, Baoding, China.
Fan ZhangDepartment of Postgraduate, Chengde Medical University, Chengde, China.
Cong ZhangDepartment of Postgraduate, Chengde Medical University, Chengde, China.
Naijing ShiDepartment of Postgraduate, Chengde Medical University, Chengde, China.
Weina MuDepartment of Ultrasound Medicine, Baoding First Central Hospital, Baoding, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To evaluate ultrasound-based radiomic features, derived from both intratumoral and peritumoral regions, for noninvasive preoperative prediction of axillary lymph node(ALN) burden in breast cancer. Methods: This retrospective study analyzed data from 300 pathologically confirmed breast cancer patients undergoing preoperative ultrasound. The cohort was randomly divided into a training set (n = 210) and a testing set (n = 90) at a 7∶3 ratio. Primary tumor regions of interest (ROIs) were manually delineated on preoperative ultrasound images using ITK-SNAP. Peritumoral ROIs were generated by radially expanding the intratumoral ROI by 2mm, 3mm, and 4mm. A comprehensive set of radiomic features was extracted from each ROI, with feature selection via LASSO based methods. Six machine-learning classifiers were trained on intratumoral features to identify the optimal algorithm. Using this algorithm, we built: (1) A radiomics model based solely on intratumoral or peritumoral features. (2) Combined models incorporating intratumoral and peritumoral features at each expansion margin (2mm, 3mm, and 4mm). The best-performing radiomics model was then integrated with significant clinical and conventional imaging variables to construct a composite nomogram. Model discrimination was evaluated by area under the receiver operating characteristic curve (AUC), calibration was assessed via calibration curves, and clinical utility was appraised using decision curve analysis (DCA). Model interpretability was facilitated through Shapley additive explanation (SHAP) values and visualized in a nomogram. Results: A Random Forest classifier applied to combined intratumoral and 3mm peritumoral features yielded the highest AUCs (training set: 0.825; testing set: 0.746). Multivariable logistic regression identified lesion location and ultrasonographic axillary lymph node status as independent clinical predictors (p<0.05). The integrated nomogram-combining these clinical factors with the optimal radiomics signature-demonstrated superior performance (training AUC: 0.906; testing AUC: 0.818). DCA confirmed that the combined model conferred the greatest net clinical benefit across a range of threshold probabilities, and calibration curves indicated excellent agreement between predicted and observed probabilities. Discussion: A composite model integrating intratumoral and 3mm peritumoral ultrasound radiomic features with key clinical and imaging variables enables accurate, noninvasive preoperative prediction of ALN burden in breast cancer. This approach may serve as a valuable decision support tool to guide individualized surgical planning.

Indexed as

axillary lymph node burdenbreast cancerperitumoral regionradiomicsultrasound

Identifiers

PMID41613541
PMCPMC12847015

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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.