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Updated: Apr 8, 2026

Proton Therapy Delivery and Its Clinical Application in Select Solid Tumor Malignancies
Published on: February 6, 2019
Moderate hypofractionation: long-term toxicity results of prostate bed radiotherapy (FRAME-PROSTATE)
Federico Camilli1, Saverio Caini2, Chiara Doccioli3
1Radiation Oncology Section, Department of Medicine and Surgery, University of Perugia and Perugia General Hospital, Ospedale Santa Maria Della Misericordia, Piazzale Menghini 1, 06132, Perugia, Italy.
Purpose:
Moderately hypofractionated radiotherapy (m-HRT) is a standard of care in the radical treatment of localized prostate cancer (PCa). Still, its role after radical prostatectomy (RP) is yet to be defined. We present long-term outcome and toxicity results of m-HRT in the post-prostatectomy setting.
Methods And Patients:
Retrospective analysis of 172 PCa patients treated with daily volumetric image-guided Tomotherapy-based m-HRT between 2013 and 2020. For outcome and toxicity endpoints, we used Kaplan-Meier survival curves and the chi-square test for univariate analysis.
Results:
The median time from RP to m-HRT was 11 months (interquartile [IQR], 8.3-31.4). The median total dose to the prostate bed was 69.75 Gy (IQR, 65.25-72 Gy) (2.25 Gy per fraction). With a median follow-up of 8.25 years (IQR 7.06-9.17 years), 10-year overall survival (OS), metastasis-free survival (MFS), and biochemical relapse-free survival (b-RFS) were 98.8% (95% CI, 95.4-99.7), 85.9% (95% CI, 79.7-90.3), and 82.4% (95% CI, 75.8-87.3), respectively. Late genitourinary (GU) toxicity of grade ≥ 2 was observed in 14 (8.1%) patients. The 10-year freedom from late grade ≥ 2 GU toxicity was 89.8% (95% CI, 83.2-93.8%). Late gastrointestinal (GI) toxicity grade ≥ 2 was reported in 2 (1.1%) patients. The 10-year freedom from late grade ≥ 2 GI toxicity was 98.8% (95% CI, 95.3-99.7%). At univariate analysis, acute GU toxicity was associated with late GU toxicity (p = 0.016).
Conclusions:
Our long-term results confirm the critical role of modern radiotherapy in curing PCa in the post-operative setting, reducing overall treatment time and the risk of toxicity.
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