Evidence map›Paper›PMID 39822358›Full record

ArticleGland surgery2024

Intranodular and perinodular ultrasound radiomics distinguishes benign and malignant thyroid nodules: a multicenter study.

Xuelin Zhu, Jing Li, Hao Li, Kaifeng Wang, Jian Zhang, Jian Meng, Rong Wu, Meilan Zhang, Hai Du

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Article in Gland surgery, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

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0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

Who cites it

7 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Xuelin Zhu *The Faculty of Medicine, Qilu Institute of Technology, Jinan, China.
Jing Li *Graduate School, Baotou Medical College, Baotou, China.
Hao LiThe Faculty of Medicine, Qilu Institute of Technology, Jinan, China.
Kaifeng WangThe Second Clinical Medical College of Fujian Medical University, Fuzhou, China.
Jian ZhangDepartment of Imaging, The Affiliated Taizhou People's Hospital of Nanjing Medical University, Taizhou, China.
Jian MengDepartment of Ultrasound, North China University of Science and Technology Affiliated Hospital, Tangshan, China.
Rong WuDepartment of Ultrasound, Ordos Central Hospital, Ordos, China.
Meilan ZhangGraduate School, Baotou Medical College, Baotou, China.
Hai DuDepartment of Radiology, Ordos Central Hospital, Ordos, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Ultrasound based radiomics prediction model can improve the differentiation ability of benign and malignant thyroid nodules to avoid overtreatment. This study evaluates the role of predictive models based on intranodular and perinodular ultrasound radiomics in distinguishing between benign and malignant thyroid nodules. Methods: A total of 1,076 thyroid nodules were enrolled from three hospitals between 2016 and 2022, forming the training, validation and test cohorts. The clinical signature (Clinic_Sig) was developed based on clinical information and conventional morphological features of ultrasound. Expanding 1 pixel, 3 pixels, 5 pixels, 7 pixels, and 9 pixels outward from the thyroid nodule, six radiomics models were constructed using intranodular (intra) and combined radiomics (intranodular and perinodular: +p1,+p3,+p5,+p7,+p9) features. The model with the best area under the curve (AUC) was defined as radiomics signature (Rad_Sig). The combined model was constructed from Clinic_Sig and Rad_Sig. AUC and calibration curves were used to evaluate the predictive performance of the model. Decision curve analysis (DCA) was used to evaluate the clinical net benefit of the model. Results: The intra+p1 radiomics model exhibited the highest efficacy (AUC =0.863) in the test cohort, which was combined with Clinic_Sig to construct the combined model. Compared with Clinic_Sig and Rad_Sig, the combined model showed the higher predictive performance, with AUCs of 0.942 (training), 0.894 (validation), and 0.933 (test). The calibration curve showed that the predicted probabilities of the combined model were in good agreement with the actual probabilities, and DCA indicated that it provided more net benefit than the treat-none or treat-all scheme. Conclusions: The combined model based on clinical signatures, intranodular and perinodular ultrasound radiomics has the potential to effectively predict benign or malignant thyroid nodules.

Indexed as

Intranodularperinodularradiomicsthyroid nodulesultrasound

Identifiers

PMID39822358
PMCPMC11733639

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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.