Exploring the Association of Imaging and Tumor Microenvironment in Urologic Cancer Using Radiogenomic Approach(Radiogenomics-Urinary)

July 31, 2024 updated by: Wuhan Union Hospital, China
This is the prospective, observational cohort study (Radiogenomics-Urinary), which aims to explore the relationship between the imaging information of urologic cancer patients, tumor microenvironment and the prognosis of urologic cancer patients.

Study Overview

Status

Recruiting

Conditions

Study Type

Observational

Enrollment (Estimated)

150

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Hubei
      • Wuhan, Hubei, China, 430000
        • Recruiting
        • Union Hospital,Tongji Medical College,Huazhong University of Science and Technology
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Patients treated for urologic cancer

Description

Inclusion Criteria:

  1. Patients treated for urologic cancer in Wuhan Union Hospital from August 2024 to August 2027;
  2. Aged > 18 years old;
  3. At least one CT scan or MRI scan before treatment;
  4. Tissue biopsy pathological examination confirmed the diagnosis of the above tumors.

Exclusion criteria:

  1. Poor image quality;
  2. Incomplete clinical data or loss of follow-up;
  3. Presence of another primary malignancy other than urologic cancer;
  4. Unclear pathological diagnosis。

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Correlation analysis of sequencing results and body composition
Time Frame: 0.5 year
Conducting correlation analysis between body composition and results of multi-omics sequencing.
0.5 year
Correlation analysis of sequencing results and tumor radiomic features
Time Frame: 0.5 year
Conducting correlation analysis between radiomic features and results of multi-omics sequencing.
0.5 year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Constructing tumor microenvironment prediction model
Time Frame: 2 years
Constructing radiomic model to predict tumor microenvironment. The indicator is the area under the curve (AUC) of the prediction model
2 years
Constructing a multi-dimensional prognostic prediction model
Time Frame: 3 years
A high-dimensional model was constructed to predict the prognosis of patients through multi-omics sequencing data, body composition, and tumor radiomic features. The indicator is the area under the curve (AUC) of the prediction model.
3 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

August 1, 2024

Primary Completion (Estimated)

August 1, 2027

Study Completion (Estimated)

August 1, 2027

Study Registration Dates

First Submitted

July 31, 2024

First Submitted That Met QC Criteria

July 31, 2024

First Posted (Estimated)

August 5, 2024

Study Record Updates

Last Update Posted (Estimated)

August 5, 2024

Last Update Submitted That Met QC Criteria

July 31, 2024

Last Verified

July 1, 2024

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Urologic Cancer

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