Evidence map›Paper›PMID 40691342›Full record

ArticleEuropean radiology experimental2025

Deep learning using nasal endoscopy and T2-weighted MRI for prediction of sinonasal inverted papilloma-associated squamous cell carcinoma: an exploratory study.

Jiliang Ren, Zhe Ren, Duo Zhang, Ying Yuan, Meng Qi

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Article in European radiology experimental, 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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5 · Who and what money

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5 authors.

Jiliang Ren *Department of Radiology, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Zhe Ren *Department of Radiology, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Duo ZhangDepartment of Otolaryngology-HNS, Eye & ENT Hospital, Fudan University, Shanghai, China.
Ying YuanDepartment of Radiology, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China. yuany83@163.com.
Meng QiDepartment of Radiology, Eye & ENT Hospital, Fudan University, Shanghai, China. 13817265738@163.com.ORCID http://orcid.org/0009-0007-8256-6532

Funding

National Scientific Foundation of China 82101992National Scientific Foundation of China 82172051Shanghai Municipal Health Commission 20194Y0104Shanghai Ninth People's Hospital 2022hbyjxys-rjl
6 · The paper itself

Abstract

backgroundDetecting malignant transformation of sinonasal inverted papilloma (SIP) into squamous cell carcinoma (SIP-SCC) before surgery is a clinical need. We aimed to explore the value of deep learning (DL) that leverages nasal endoscopy and T2-weighted magnetic resonance imaging (T2W-MRI) for automated tumor segmentation and differentiation between SIP and SIP-SCC.

methodsWe conducted a retrospective analysis of 174 patients diagnosed with SIPs, who were divided into a training cohort (n = 121) and a testing cohort (n = 53). Three DL architectures were utilized to train automated segmentation models for endoscopic and T2W-MRI images. DL scores predicting SIP-SCC were generated using DenseNet121 from both modalities and combined to create a dual-modality DL nomogram. The diagnostic performance of the DL models was assessed alongside two radiologists, evaluated through the area under the receiver operating characteristic curve (AUROC), with comparisons made using the Delong method.

resultsIn the testing cohort, the FCN_ResNet101 and VNet exhibited superior performance in automated segmentation, achieving mean dice similarity coefficients of 0.95 ± 0.03 for endoscopy and 0.93 ± 0.02 for T2W-MRI, respectively. The dual-modality DL nomogram based on automated segmentation demonstrated the highest predictive performance for SIP-SCC (AUROC 0.865), outperforming the radiology resident (AUROC 0.672, p = 0.071) and the attending radiologist (AUROC 0.707, p = 0.066), with a trend toward significance. Notably, both radiologists improved their diagnostic performance with the assistance of the DL nomogram (AUROCs 0.734 and 0.834).

conclusionThe DL framework integrating endoscopy and T2W-MRI offers a fully automated predictive tool for SIP-SCC. RELEVANCE STATEMENT: The integration of endoscopy and T2W-MRI within a well-established DL framework enables fully automated prediction of SIP-SSC, potentially improving decision-making for patients with suspicious SIP. KEY POINTS: Detecting the transformation of SIP into SIP-SCC before surgery is both critical and challenging. Endoscopy and T2W-MRI were integrated using DL for predicting SIP-SCC. The dual-modality DL nomogram outperformed two radiologists. The nomogram may improve decision-making for patients with suspicious SIP.

Indexed as

Carcinoma, Squamous CellDeep LearningEndoscopyMagnetic Resonance ImagingNose NeoplasmsPapilloma, InvertedParanasal Sinus NeoplasmsAdultAgedFemaleHumansMaleMiddle AgedNomogramsRetrospective StudiesDeep learningEndoscopyMagnetic resonance imagingSinonasal inverted papillomaSquamous cell carcinoma

Identifiers

PMID40691342
PMCPMC12279620

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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.