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

2. června 2026 aktualizováno: 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.

Přehled studie

Postavení

Zatím nenabíráme

Detailní popis

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 studie

Pozorovací

Zápis (Odhadovaný)

500

Kritéria účasti

Výzkumníci hledají lidi, kteří odpovídají určitému popisu, kterému se říká kritéria způsobilosti. Některé příklady těchto kritérií jsou celkový zdravotní stav osoby nebo předchozí léčba.

Kritéria způsobilosti

Věk způsobilý ke studiu

  • Dospělý
  • Starší dospělý

Přijímá zdravé dobrovolníky

Ano

Metoda odběru vzorků

Vzorek nepravděpodobnosti

Studijní populace

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.

Popis

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)

Studijní plán

Tato část poskytuje podrobnosti o studijním plánu, včetně toho, jak je studie navržena a co studie měří.

Jak je studie koncipována?

Detaily designu

Kohorty a intervence

Skupina / 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 je měření studie?

Primární výstupní opatření

Měření výsledku
Popis opatření
Časové okno
Area Under the Curve (AUC) of the multimodal AI fusion diagnostic system
Časové okno: 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).

Sekundární výstupní opatření

Měření výsledku
Popis opatření
Časové okno
Sensitivity and Specificity of the Multimodal AI Fusion Diagnostic System
Časové okno: 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).

Spolupracovníci a vyšetřovatelé

Zde najdete lidi a organizace zapojené do této studie.

Publikace a užitečné odkazy

Osoba odpovědná za zadávání informací o studiu tyto publikace poskytuje dobrovolně. Mohou se týkat čehokoli, co souvisí se studiem.

Obecné publikace

Termíny studijních záznamů

Tato data sledují průběh záznamů studie a předkládání souhrnných výsledků na ClinicalTrials.gov. Záznamy ze studií a hlášené výsledky jsou před zveřejněním na veřejné webové stránce přezkoumány Národní lékařskou knihovnou (NLM), aby se ujistily, že splňují specifické standardy kontroly kvality.

Hlavní termíny studia

Začátek studia (Odhadovaný)

1. června 2026

Primární dokončení (Odhadovaný)

1. června 2028

Dokončení studie (Odhadovaný)

1. června 2028

Termíny zápisu do studia

První předloženo

2. června 2026

První předloženo, které splnilo kritéria kontroly kvality

2. června 2026

První zveřejněno (Aktuální)

8. června 2026

Aktualizace studijních záznamů

Poslední zveřejněná aktualizace (Aktuální)

8. června 2026

Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality

2. června 2026

Naposledy ověřeno

1. června 2026

Více informací

Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .

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