Optimization of Management for Sporadic Bilateral Renal Cell Carcinoma
- Conditions
- Kidney Cancer
- Interventions
- Procedure: Surgery treatment or local tumor destruction.
- Registration Number
- NCT06369519
- Lead Sponsor
- Peking University First Hospital
- Brief Summary
Sporadic bilateral renal cell carcinoma (BRCC) is a rare situation of RCC. The treatment for BRCC is controversial and there is a lack of authoritative guidelines about the management of BRCC. The goal of this cohort study is to identify prognostic factors, construct predictive nomograms, and optimize management for sporadic BRCC patients. The main questions it aims to answer are:
What are the factors influencing the prognosis of BRCC patients? What's the appropriate treatment for BRCC patients?
Researchers will analysis the prognostic factors and compare the prognosis of BRCC patients receiving different treatments.
- Detailed Description
Sporadic bilateral renal cell carcinoma (BRCC) is a rare situation of RCC. The treatment for BRCC is controversial and there is a lack of authoritative guidelines about the management of BRCC. This cohort study aims to identify prognostic factors, construct predictive nomograms, and optimize surgical treatment for sporadic BRCC patients. The main questions it aims to answer are:
What are the factors influencing the prognosis of BRCC patients? What's the appropriate treatment for BRCC patients? In this retrospective population-based cohort study, patients diagnosed with sporadic BRCC between 2000 and 2020 were identified from the Surveillance, Epidemiology, and End Results (SEER) database. Researchers will analysis the prognostic factors and compare the prognosis of BRCC patients receiving different treatments.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 3677
- Age ≥ 18 years.
- Clinical diagnosis of localized BRCC (M0) from 2000 to 2020.
- Active follow-up.
- Complete clinicopathological information.
- Diagnosed by autopsy or death certificate only.
- Tending to suffer from hereditary RCC, including those complicating with pancreatic neuroendocrine tumor (pNET) or hemangioblastoma.
- Unavailable key information.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Synchronous BRCC patients Surgery treatment or local tumor destruction. Synchronous BRCC is defined as the second primary RCC emerges within 6 months from the diagnosis of the first primary RCC. Metachronous BRCC patients Surgery treatment or local tumor destruction. Metachronous BRCC develops beyond 6 months from the diagnosis of the first primary RCC.
- Primary Outcome Measures
Name Time Method Overall survival (OS) From date of diagnosis of the second primary RCC until the date of death from any cause or the date of last follow-up, whichever came first, assessed up to 20 years. OS was calculated as the time interval from the diagnosis of the second primary RCC to death or the time to the last follow-up.
- Secondary Outcome Measures
Name Time Method Cancer-specific survival (CSS) From date of diagnosis of the second primary RCC until the date of death from the same disease or the date of last follow-up, whichever came first, assessed up to 20 years. CSS was calculated as the time interval from the diagnosis of the second primary RCC to death from the same disease or the last follow-up.
Trial Locations
- Locations (1)
Peking University First Hospital
🇨🇳Beijing, Beijing, China