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Defining bowel dose volume constraints for bladder radiotherapy treatment planning
F McDonald1, R Waters2, S Gulliford3
1Academic Radiotherapy Unit, Institute of Cancer Research, London, UK; The Royal Marsden NHS Foundation Trust, Sutton, Surrey, UK.
Summary
Radiotherapy dose escalation for bladder cancer is limited by normal tissue effects. This study found that larger bowel volumes receiving radiation correlate with increased late bowel toxicity, proposing new dose constraints to minimize risks.
Area of Science:
- Radiation oncology
- Clinical oncology
- Medical physics
Background:
- Radiotherapy dose escalation for muscle-invasive bladder cancer is limited by normal tissue toxicity.
- Understanding the relationship between radiation dose to the bowel and late toxicity is crucial for treatment planning.
Purpose of the Study:
- To assess the relationship between bowel dose-volume data and late bowel toxicity in patients with muscle-invasive bladder cancer treated with radical radiotherapy.
- To develop a model to predict the probability of late bowel toxicity based on absolute bowel volumes.
Main Methods:
- Retrospective contouring of the bowel on radiotherapy plans from 47 patients in the BC2001 trial.
- Exploration of the relationship between bowel volume at various dose levels and prospectively collected late bowel toxicity data.
Main Results:
- 15% and 6% of patients experienced grade 1 and grade 2 or higher late bowel toxicity, respectively.
- Reduced high-dose volume radiotherapy resulted in significantly smaller mean bowel volumes at doses ≥50 Gy compared to standard radiotherapy.
- Increased bowel volume correlated with a higher probability of late bowel toxicity (P ≤ 0.05 for 30-50 Gy dose levels).
- No grade 2+ toxicity was observed below proposed thresholds for 25% probability of late bowel toxicity.
Conclusions:
- A clear dose-volume effect exists for late bowel toxicity in radical bladder radiotherapy.
- A predictive model for late bowel toxicity probability based on absolute bowel volumes is presented to aid clinicians in treatment planning.
- Proposed dose-volume constraints, predicting a 25% probability of late bowel toxicity, are suggested for clinical use.

