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Intelligent Screening and Precision Diagnosis of Prostate Cancer Based on Multimodal Data

2026年6月15日 更新者:Fubo Wang、Guangxi Medical University

Prospective Validation of an AI-Assisted Multimodal Imaging-Pathology Fusion System for Precision Diagnosis and Biopsy Guidance in Patients With Suspected Prostate Cancer

This project aims to develop a precision screening and diagnostic solution for prostate cancer based on multimodal artificial intelligence, focusing on addressing the diagnostic challenge in patients within the PSA "gray zone" of 4-10 ng/mL. The project will integrate multidimensional information including ctDNA liquid biopsy, routine laboratory data, and prostate ultrasound images to develop three models: a ctDNA-based multimodal AI prediction model, a routine laboratory data-assisted decision model, and an ultrasound image AI-assisted diagnostic model. On this basis, a multimodal AI fusion decision system will be established to automatically generate individualized risk assessment reports and diagnostic recommendations. Additionally, a closed-loop mechanism of "clinical use - data feedback - model optimization" will be constructed to continuously iterate model parameters using pathological gold standards, thereby improving predictive accuracy in our hospital population. The project will form a generalizable precision diagnostic workflow, reduce unnecessary biopsies in "gray zone" patients, and provide an implementable in-hospital solution for precision medicine in prostate cancer.

研究概览

地位

主动,不招人

详细说明

Background: Prostate cancer (PCa) is the second most common malignancy in men worldwide. In China, the average annual growth rate of PCa incidence is as high as 7.2%. Current diagnostic pathways rely on transrectal ultrasound (TRUS)-guided prostate biopsy. However, serum PSA, the main decision-making indicator for biopsy, is not cancer-specific and has severely insufficient specificity. Many men with elevated PSA undergo unnecessary invasive biopsies. The diagnostic challenge is particularly prominent in the PSA "gray zone" of 4-10 ng/mL.

Objectives: This study aims to develop a precision screening and diagnostic solution for prostate cancer based on multimodal artificial intelligence, focusing on addressing the diagnostic challenge in patients within the PSA gray zone. Specific objectives include: (1) improving screening efficiency to quickly identify high-risk individuals and avoid over-examination; (2) solving the diagnostic gray zone problem; (3) reducing unnecessary biopsies through non-invasive or minimally invasive precision tools; and (4) achieving personalized management through risk stratification.

Study Design: Prospective enrollment of suspected prostate cancer patients. Total sample size is no less than 500 cases, divided into training set (approximately 400 cases) and validation set (approximately 100 cases) at an 8:2 ratio.

Eligibility Criteria:

Inclusion criteria: (1) age ≥45 years, male; (2) presenting with abnormal serum PSA (≥4 ng/mL), abnormal digital rectal examination, or suspicious lesions on prostate ultrasound; (3) undergoing prostate biopsy with definitive pathological results; (4) signed informed consent.

Exclusion criteria: (1) previously diagnosed with prostate cancer and receiving surgery, radiotherapy, or endocrine therapy; (2) with other malignancies; (3) critical missing clinical data (e.g., missing PSA value, incomplete ultrasound report).

Study Interventions/Assessments: All enrolled patients complete the following data collection: (1) serum PSA and free PSA; (2) routine laboratory tests including complete blood count, liver and kidney function; (3) transrectal or transabdominal prostate ultrasound with images stored in DICOM format and prostate volume recorded; (4) post-prostate massage urine for ctDNA methylation target detection; (5) digital rectal examination results, age, family history, medical history; (6) pathological diagnosis results from biopsy as gold standard.

Models to be Developed:

Tool 1 - ctDNA multimodal AI prediction model: using ctDNA methylation results combined with age, PSA, and prostate volume. Logistic regression and random forest will be compared.

Tool 2 - Routine laboratory data-assisted decision model: integrating structured data including complete blood count, liver and kidney function, PSA, free PSA, age, and prostate volume. XGBoost and LightGBM with LASSO feature reduction will be used.

Tool 3 - Prostate ultrasound image AI-assisted diagnostic model: using convolutional neural network (ResNet or DenseNet architecture) for deep learning modeling. The model outputs lesion probability heatmaps and malignancy probability scores.

Multimodal Fusion Strategy: The three model outputs will be combined according to preset fusion rules to generate comprehensive risk stratification (low/moderate/high concern). Diagnostic sensitivity, specificity, positive predictive value, negative predictive value, and AUC of the fusion solution will be calculated using pathological results as gold standard. The AUC will be compared with that of PSA alone using DeLong test. Stratified analysis will be performed for the PSA 4-10 ng/mL gray zone subgroup. Decision curve analysis (DCA) will be used to evaluate clinical net benefit.

Closed-loop Optimization: All pathological results will be periodically returned to the model management system in a de-identified manner, and quarterly iterative optimization of the three specialized models and fusion rules will be conducted.

Study Duration: May 2026 to May 2028 (approximately 2 years).

Funding: This is a hospital-level research project with an application fund of 50,000 RMB.

研究类型

观察性的

注册 (估计的)

500

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Guangxi
      • Nan'ning、Guangxi、中国
        • Guangxi Medical University First Affiliated Hospital

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

是的

取样方法

非概率样本

研究人群

The study population consists of male patients aged ≥45 years with suspected prostate cancer, presenting with abnormal serum PSA (≥4 ng/mL), abnormal digital rectal examination, or suspicious lesions on prostate ultrasound, who are scheduled to undergo prostate biopsy. Participants will be prospectively enrolled from patients presenting to the hospital for PSA abnormality, lower urinary tract symptoms, or active screening.

The total planned sample size is no less than 500 cases, divided into a training set (approximately 400 cases) and a validation set (approximately 100 cases) at an 8:2 ratio.

Excluded are patients with prior diagnosis of prostate cancer receiving active treatment, those with other malignancies, and those with critical missing clinical data.

描述

Inclusion Criteria:

  1. Age ≥45 years, male
  2. Presenting with abnormal serum PSA (≥4 ng/mL), abnormal digital rectal examination, or suspicious lesions on prostate ultrasound
  3. Undergoing prostate biopsy with definitive pathological results
  4. Signed informed consent

Exclusion Criteria:

  1. Previously diagnosed with prostate cancer and receiving surgery, radiotherapy, or endocrine therapy
  2. With other malignancies
  3. Critical missing clinical data (e.g., missing PSA value, incomplete ultrasound report)

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

队列和干预

团体/队列
Training Set
Approximately 400 cases. This group will be used to develop and internally validate the three specialized models: (1) ctDNA multimodal AI prediction model, (2) routine laboratory data-assisted decision model, and (3) prostate ultrasound image AI-assisted diagnostic model. Five-fold cross-validation will be used for algorithm comparison and hyperparameter tuning.
Validation Set
Approximately 100 cases. This independent validation set will be used to evaluate the diagnostic performance of the multimodal fusion decision system. Sensitivity, specificity, positive predictive value, negative predictive value, and AUC will be calculated using pathological results as the gold standard. DeLong test will be used to compare AUC with PSA alone. Decision curve analysis (DCA) will be used to evaluate clinical net benefit. Subgroup analysis will be performed for the PSA 4-10 ng/mL gray zone.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Area Under the Curve (AUC) of the multimodal AI fusion diagnostic system
大体时间:Measured after all participants have completed biopsy and obtained pathological diagnosis (approximately within the 2-year study period).
The AUC of the fusion model in distinguishing clinically significant prostate cancer from non-cancer or indolent cancer, using pathological biopsy results as the gold standard.
Measured after all participants have completed biopsy and obtained pathological diagnosis (approximately within the 2-year study period).

次要结果测量

结果测量
措施说明
大体时间
Sensitivity and Specificity of the Multimodal AI Fusion Diagnostic System
大体时间:Measured after all participants have completed biopsy and obtained pathological diagnosis (approximately within the 2-year study period).
The sensitivity and specificity of the fusion model in detecting clinically significant prostate cancer, using pathological biopsy results as the gold standard.
Measured after all participants have completed biopsy and obtained pathological diagnosis (approximately within the 2-year study period).

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2026年5月1日

初级完成 (估计的)

2028年5月1日

研究完成 (估计的)

2028年5月1日

研究注册日期

首次提交

2026年6月2日

首先提交符合 QC 标准的

2026年6月2日

首次发布 (实际的)

2026年6月8日

研究记录更新

最后更新发布 (实际的)

2026年6月17日

上次提交的符合 QC 标准的更新

2026年6月15日

最后验证

2026年5月1日

更多信息

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