This study is the first prospective, randomized phase III clinical trial designed to evaluate whether ultrahypofractionated radiotherapy is non-inferior to conventionally moderately hypofractionated radiotherapy in terms of efficacy, with acceptable toxicity, in patients who develop biochemical recurrence following radical prostatectomy. Considering the potential clinical benefits of shorter treatment duration, cost reduction, and improved patient convenience, this study is expected to provide important evidence to optimize salvage radiotherapy strategies in routine clinical practice.
Moderate hypofractionated radiotherapy (Moderate-hypoRT): 60 Gy in 24 fractions, delivered once daily, 5 days per week (on weekdays), over a total of 5-6 weeks. Ultra-hypofractionated radiotherapy (Ultra-hypoRT): 31 Gy in 5 fractions, delivered every other day (2-3 fractions per week), over a total of 2 weeks.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
270
Moderate hypofractionated radiotherapy (Moderate-hypoRT): 60 Gy in 24 fractions (administered once daily on weekdays, five times per week, over a total of 5-6 weeks).
Ultra-hypofractionated radiotherapy (Ultra-hypoRT): 31 Gy in 5 fractions (administered every other day, 2-3 times per week, over a total of 2 weeks).
Samsung Medical Center
Seoul, Gangnam-gu, South Korea
RECRUITING5-year biochemical progression-free survival (bPFS)
Time frame: 5 years after treatment completion
Analyze Distant Metastasis-Free Survival (DMFS)
Time frame: 5 years after treatment completion
Cancer-Specific Survival (CSS)
Time frame: 5 years after treatment completion
Overall Survival (OS)
Time frame: 5 years after treatment completion
Compare acute and late Genitourinary (GU) and Gastrointestinal (GI) toxicities.
Time frame: 5 years after treatment completion
Compare patient-reported Quality of Life (QoL) outcomes
Time frame: During treatment and follow-up
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