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

2. Juni 2026 aktualisiert von: 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.

Studienübersicht

Status

Noch keine Rekrutierung

Detaillierte Beschreibung

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.

Studientyp

Beobachtungs

Einschreibung (Geschätzt)

500

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Erwachsene
  • Älterer Erwachsener

Akzeptiert gesunde Freiwillige

Ja

Probenahmeverfahren

Nicht-Wahrscheinlichkeitsprobe

Studienpopulation

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.

Beschreibung

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)

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

Kohorten und Interventionen

Gruppe / Kohorte
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.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Area Under the Curve (AUC) of the multimodal AI fusion diagnostic system
Zeitfenster: 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).

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Sensitivity and Specificity of the Multimodal AI Fusion Diagnostic System
Zeitfenster: 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).

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Publikationen und hilfreiche Links

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Allgemeine Veröffentlichungen

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

1. Juni 2026

Primärer Abschluss (Geschätzt)

1. Juni 2028

Studienabschluss (Geschätzt)

1. Juni 2028

Studienanmeldedaten

Zuerst eingereicht

2. Juni 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

2. Juni 2026

Zuerst gepostet (Tatsächlich)

8. Juni 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

8. Juni 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

2. Juni 2026

Zuletzt verifiziert

1. Juni 2026

Mehr Informationen

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