Prediction of adverse pathology in prostate cancer using a multimodal deep learning approach based on [<sup>18</sup>F]PSMA-1007 PET/CT and multiparametric MRI.
Authors
Affiliations (7)
Affiliations (7)
- The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, China.
- The Department of Radiology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, China.
- Cixi Biomedical Research Institute, Wenzhou Medical University, Zhejiang, 315300, China.
- The Department of Nuclear Medicine, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, China.
- The Department of Urology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, China.
- The Department of Nuclear Medicine, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, China. [email protected].
- The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, China. [email protected].
Abstract
Accurate prediction of adverse pathology (AP) in prostate cancer (PCa) patients is crucial for formulating effective treatment strategies. This study aims to develop and evaluate a multimodal deep learning model based on [<sup>18</sup>F]PSMA-1007 PET/CT and multiparametric MRI (mpMRI) to predict the presence of AP, and investigate whether the model that integrates [<sup>18</sup>F]PSMA-1007 PET/CT and mpMRI outperforms the individual PET/CT or mpMRI models in predicting AP. 341 PCa patients who underwent radical prostatectomy (RP) with mpMRI and PET/CT scans were retrospectively analyzed. We generated deep learning signature from mpMRI and PET/CT with a multimodal deep learning model (MPC) based on convolutional neural networks and transformer, which was subsequently incorporated with clinical characteristics to construct an integrated model (MPCC). These models were compared with clinical models and single mpMRI or PET/CT models. The MPCC model showed the best performance in predicting AP (AUC, 0.955 [95% CI: 0.932-0.975]), which is higher than MPC model (AUC, 0.930 [95% CI: 0.901-0.955]). The performance of the MPC model is better than that of single PET/CT (AUC, 0.813 [95% CI: 0.780-0.845]) or mpMRI (AUC, 0.865 [95% CI: 0.829-0.901]). Additionally, MPCC model is also effective in predicting single adverse pathological features. The deep learning model that integrates mpMRI and [<sup>18</sup>F]PSMA-1007 PET/CT enhances the predictive capabilities for the presence of AP in PCa patients. This improvement aids physicians in making informed preoperative decisions, ultimately enhancing patient prognosis.