Evidence map›Paper›PMID 41971125›Full record

ArticleTranslational andrology and urology2026

Radiomics and deep learning fusion model based on multiphasic CT for predicting HER2 expression status in bladder urothelial carcinoma: a multicenter study.

Wenbang Pan, Liu Yang, Lin Yang, Chaohui Gu, Qiang Lv, Yingyi Zhang, Mingyue Li

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Article in Translational andrology and urology, 2026. 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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7 authors.

Wenbang Pan *Department of General Surgery, Dalian Second People's Hospital, Dalian, China.
Liu Yang *Department of General Surgery, Dalian Second People's Hospital, Dalian, China.
Lin YangDepartment of General Surgery, Dalian Second People's Hospital, Dalian, China.
Chaohui GuDepartment of Urology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Qiang LvDepartment of Urology, The First Affiliated Hospital with Nanjing Medical University, Nanjing, China.
Yingyi ZhangDepartment of General Surgery, Dalian Second People's Hospital, Dalian, China.
Mingyue LiDepartment of General Surgery, Dalian Second People's Hospital, Dalian, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Human epidermal growth factor receptor 2 (HER2) overexpression is a key therapeutic target for novel antibody-drug conjugates (ADCs) like disitamab vedotin (RC48) in bladder urothelial carcinoma (BLCA), but immunohistochemistry-based assessment is limited by intratumoral heterogeneity and sampling bias. A noninvasive and reliable imaging-based approach is therefore urgently needed. Therefore, this study aimed to construct a noninvasive, imaging-based multimodal model for predicting HER2 expression status in BLCA using tri-phasic CT. Methods: A total of 411 patients from three institutions (2021-2024) who underwent tri-phasic contrast-enhanced computed tomography (CT) and HER2 immunohistochemistry (IHC) were included. Patients were classified as HER2-positive (IHC 2+/3+) or negative (IHC 0/1+) based on therapeutic criteria for ADCs. Patients were divided into training, internal validation, and external validation cohorts. Radiomics models, 2.5D and 3D ResNet50 deep learning models, a clinical model, and a multimodal fusion model were developed. Model performance was evaluated using receiver operating characteristic (ROC) analysis, calibration curves, and decision curve analysis. Results: Tumor architecture (sessile pattern), hydronephrosis, pelvic pain, and radiological lymph node status were identified as independent predictors of HER2 positivity. The 2.5D ResNet50 model achieved an external area under the curve (AUC) of 0.827, significantly outperforming the 3D model (AUC =0.608). The multimodal fusion model showed the best performance, with AUCs of 0.960, 0.908, and 0.873 in the training, internal validation, and external validation cohorts, respectively. In the external cohort, accuracy, sensitivity, and specificity were 0.819, 0.857, and 0.784. The multimodal model significantly outperformed all single-modality models. Conclusions: A tri-phasic CT-based multimodal model enables noninvasive assessment of HER2 expression status in BLCA, providing a promising tool for selection of patients likely to benefit from ADC therapy.

Indexed as

Bladder urothelial carcinoma (BLCA)computed tomography (CT)deep learninghuman epidermal growth factor receptor 2 (HER2)radiomics

Identifiers

PMID41971125
PMCPMC13062831

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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.