MedPath

Optimization of Management for Sporadic Bilateral Renal Cell Carcinoma

Completed
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
Inclusion Criteria
  • Age ≥ 18 years.
  • Clinical diagnosis of localized BRCC (M0) from 2000 to 2020.
  • Active follow-up.
  • Complete clinicopathological information.
Exclusion Criteria
  • 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
GroupInterventionDescription
Synchronous BRCC patientsSurgery 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 patientsSurgery treatment or local tumor destruction.Metachronous BRCC develops beyond 6 months from the diagnosis of the first primary RCC.
Primary Outcome Measures
NameTimeMethod
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
NameTimeMethod
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

© Copyright 2025. All Rights Reserved by MedPath