bioRxivBioengineeringPreprint
A cross-modal generative model for incomplete and degradedprostate MRI with multicentre clinical validation
Siyuan MaiD, Liang He, Mengying Zhu, Yi ChaiiD, Mengyao LyuiD, Haowei Wang, Qizhen LaniD, HaoBo Sun, Qixin ZhangiD, Jingli CheniD, Xiaobing Wei, Jiaming Liu, Guiqin Liu, Qianwen ZhangiD, Yang LiuiD, Dacheng TaoiD, Guangyu WuiD
Abstract
Missing or degraded sequences can limit prostate multiparametric MRI. We developed MSCNet, a sequence-conditioned cross-modal generative framework for reconstructing unavailable contrasts and restoring degraded acquisitions. Across ten completion tasks, task-specific MSCNet achieved mean structural similarity of 0.818 versus 0.798 for the strongest task-matched comparators; matched-capacity analyses showed larger differences in lesion fidelity and boundary preservation. In a blinded 1,000-case reader study, overall image quality met the prespecified non-inferiority criterion for DWI, ADC and T2W completion, but not T1W. In a separate 200-case diagnostic assessment, AUCs for clinically significant cancer were 0.860 with acquired images, 0.841 with MSCNet and 0.797 with baseline-generated images. A locked 186-case three-hospital cohort supported multicentre transportability. These retrospective results support quality-controlled cross-modal reconstruction as an adjunct to acquired prostate MRI.
- assay: imaging
- assay: fluorescence / live-cell microscopy
- research focus: imputation
- research focus: benchmarking
- research focus: differential expression
- approach: deep learning
- approach: large language model
- Citations
- 0
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