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Developing a Novel Prognostic Model Based on Muscle-Invasive Bladder Cancer Types: A Multicenter Retrospective Cohort
Shicong Lai1,2, Jianyong Liu3, Haopu Hu1,2
1Department of Urology, Peking University People's Hospital, Beijing, China.
Annals of Surgical Oncology
|September 16, 2024
Summary
A new prognostic model accurately predicts cancer-specific survival for muscle-invasive bladder cancer (MIBC) patients undergoing radical cystectomy. This tool aids in better patient management and clinical decisions.
Area of Science:
- Oncology
- Urology
- Cancer Genomics
Background:
- Muscle-invasive bladder cancer (MIBC) management requires accurate prognostic tools.
- Radical cystectomy (RC) and chemotherapy are standard treatments for MIBC.
- Existing models may not fully capture prognostic variability.
Purpose of the Study:
- To develop and validate a prognostic model for cancer-specific survival (CSS) in MIBC patients.
- To stratify patients into risk groups for tailored management.
- To explore biological differences between risk groups.
Main Methods:
- A prognostic model was developed using clinicopathologic and survival data from a North American cohort.
- The model was externally validated using European and Asian databases.
- Cox's proportional hazard regression was used to identify independent CSS predictors.
- Patients were classified as primary or progressive MIBC.
- Genomic and immune markers were analyzed in relation to risk groups.
Main Results:
- Tumor stage, lymph node stage, age, ethnicity, and MIBC type were significant CSS predictors.
- The developed nomogram demonstrated good predictive power, discrimination, and calibration.
- External validation confirmed the model's robustness across cohorts.
- High-risk patients exhibited significantly poorer CSS.
- High-risk group was associated with higher stromal scores, M0/M2 macrophages, and lower regulatory T cells.
Conclusions:
- The MIBC type-based nomogram offers accurate CSS predictions.
- This tool can enhance patient management and clinical decision-making for MIBC.
- Understanding immune microenvironment differences may inform future therapeutic strategies.

