First Affiliated Hospital of Fujian Medical University
Phase
Observational
Started
2024-08-01
Last updated
2026-01-12
Condition(s) studied
Renal Clear Cell CarcinomaHIF-2αRadiomicsNomogram
Study 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.
Eligibility
Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* 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
Exclusion Criteria:
* 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
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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