Predicting HIF-2α Levels in Clear Cell Kidney Cancer Using Machine Learning
Development of a Machine Learning-Based Nomogram for Predicting HIF-2α Expression Levels in Clear Cell Renal Cell Carcinoma
1 other identifier
observational
500
1 country
1
Brief Summary
This project aims to conduct a multicenter retrospective study to collect clinical, CT imaging, and pathological data from patients. A comprehensive data management system will be established, and radiomic features will be extracted to integrate and analyze multicenter data. We will develop a predictive model based on CT radiomic features and perform both internal and external cohort validation. The model will predict HIF-2α expression levels and clinically relevant prognostic factors in ccRCC, enabling precise identification of patient populations responsive to the HIF-2α antagonist Belzutifan, thereby facilitating personalized treatment decisions, minimizing unnecessary therapeutic risks, and ultimately improving patient quality of life and clinical outcomes.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Aug 2024
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 1, 2024
CompletedFirst Submitted
Initial submission to the registry
December 31, 2025
CompletedFirst Posted
Study publicly available on registry
January 12, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
September 1, 2026
January 12, 2026
December 1, 2025
2.1 years
December 31, 2025
December 31, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
HIF-2α Expression Levels in Clear Cell Renal Cell Carcinoma
1 week
Eligibility Criteria
Patients with histologically confirmed renal cell carcinoma
You may qualify if:
- Pathologically confirmed clear cell renal cell carcinoma (ccRCC)
- Availability of comprehensive clinical, pathological, and follow-up information
- Access to preoperative non-contrast and contrast-enhanced CT images through the PACS database
- Adequately preserved pathological slides for subsequent immunohistochemical (IHC) or tissue microarray analysis
- Minimum of one post-treatment follow-up with documented treatment response or efficacy evaluation
You may not qualify if:
- Patients considered ineligible for treatment owing to severe comorbid conditions or inability to undergo any therapeutic intervention
- Patients with concurrent malignancies, including prior treatment for other cancers or presence of untreated active malignancies
- Patients with inadequate CT image quality or missing imaging data
- Patients with missing or incomplete clinical, pathological, or follow-up information
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
first hospital affiliated of Fujian medical university
Fuzhou, Fujian, 350005, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 31, 2025
First Posted
January 12, 2026
Study Start
August 1, 2024
Primary Completion (Estimated)
September 1, 2026
Study Completion (Estimated)
September 1, 2026
Last Updated
January 12, 2026
Record last verified: 2025-12