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

2 czerwca 2026 zaktualizowane przez: 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.

Przegląd badań

Status

Jeszcze nie rekrutacja

Szczegółowy opis

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.

Typ studiów

Obserwacyjny

Zapisy (Szacowany)

500

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

  • Dorosły
  • Starszy dorosły

Akceptuje zdrowych ochotników

Tak

Metoda próbkowania

Próbka bez prawdopodobieństwa

Badana populacja

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.

Opis

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)

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

Kohorty i interwencje

Grupa / Kohorta
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.

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Area Under the Curve (AUC) of the multimodal AI fusion diagnostic system
Ramy czasowe: 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).

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Sensitivity and Specificity of the Multimodal AI Fusion Diagnostic System
Ramy czasowe: 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).

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Publikacje i pomocne linki

Osoba odpowiedzialna za wprowadzenie informacji o badaniu dobrowolnie udostępnia te publikacje. Mogą one dotyczyć wszystkiego, co jest związane z badaniem.

Publikacje ogólne

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Szacowany)

1 czerwca 2026

Zakończenie podstawowe (Szacowany)

1 czerwca 2028

Ukończenie studiów (Szacowany)

1 czerwca 2028

Daty rejestracji na studia

Pierwszy przesłany

2 czerwca 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

2 czerwca 2026

Pierwszy wysłany (Rzeczywisty)

8 czerwca 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

8 czerwca 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

2 czerwca 2026

Ostatnia weryfikacja

1 czerwca 2026

Więcej informacji

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