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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04220424
Other study ID # GliomaAI-6
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date November 1, 2018
Est. completion date March 1, 2022

Study information

Verified date February 2021
Source The First Affiliated Hospital of Zhengzhou University
Contact Zhenyu Zhang
Phone +86 17839973727
Email fcczhangzy1@zzu.edu.cn
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

This prospective study aims to collect clinical, radiological, pathological, molecular and genetic data including detailed clinical parameters, MR and histopathology images, molecular pathology and genetic sequencing data. By leveraging artificial intelligence, this registry seeks to construct and refine algorithms that able to predict molecular pathology or clinical outcomes of glioma patients based on MR images and histopathology images, as well as revealing related mechanisms from genetic perspective.


Description:

Non-invasive and precise prediction for molecular biomarkers such as 1p/19q co-deletion, MGMT methylation, IDH and TERTp mutations, and patients survival is challenging for gliomas. With the development of artificial intelligence, much more potential lies in the preoperative conventional/advanced MR imaging (T1 weighted imaging, T2 weighted imaging, FLAIR, contrast-enhanced T1 weighted imaging, diffusion-weighted imaging, and perfusion imaging), and in the histopathology images of HE slices of gliomas could be excavated to aid prediction of molecular pathology and patients' survival of gliomas. This study aims to collect clinical, radiological, pathological, molecular and genetic data including detailed clinical parameters, MR and histopathology images, molecular pathology (1p/19q co-deletion, MGMT methylation, IDH and TERTp mutations, etc) and genetic data (Whole exome sequencing, RNA sequencing, proteomics, etc), and seeks to construct and refine algorithms that able to predict molecular pathology or clinical outcomes of glioma patients based on MR images and histopathology images, as well as revealing related mechanisms from genetic perspective.


Recruitment information / eligibility

Status Recruiting
Enrollment 500
Est. completion date March 1, 2022
Est. primary completion date January 1, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 1 Year to 95 Years
Eligibility Inclusion Criteria: - Patients must have radiologically and histologically confirmed diagnosis of primary glioma - Life expectancy of greater than 3 months - Must receive tumor resection - Must have sufficient frozen tissues and peripheral blood samples for sequencing - Must have high-quality MR images and histopathology images - Signed informed consent Exclusion Criteria: - No gliomas - No sufficient amount of tumor tissues for detection of molecular pathology - Patients who are pregnant or breast feeding - Patients who are suffered from severe systematic malfunctions

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
MR and Histopathology images based prediction of molecular pathology and patient survival
MR and Histopathology images based prediction of molecular pathology and patient survival in gliomas by leverage artificial intelligence algorithms

Locations

Country Name City State
China Department of Neurosurgery, First Affiliated Hospital of Zhengzhou University Zhengzhou Henan

Sponsors (2)

Lead Sponsor Collaborator
The First Affiliated Hospital of Zhengzhou University Sun Yat-sen University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary AUC of Prediction performance AUC of Prediction performance=sensitivity+specificity-1 up to 2 years
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