TY - JOUR
T1 - Salvage radiotherapy after radical prostatectomy
T2 - Long-term results of urinary incontinence, toxicity and treatment outcomes
AU - van Dessel, Lisanne F.
AU - Reuvers, Sarah H. M.
AU - Bangma, Chris H.
AU - Al-Uwini, Shafak
PY - 2018/6
Y1 - 2018/6
N2 - Purpose: For patients with local recurrent disease after radical prostatectomy (35-54%) salvage radiotherapy (SRT) is the treatment of choice. In the post prostatectomy setting, SRT may impose risk at increased toxicity. As data on long-term toxicity, especially on urinary incontinence, are scarce, we report on the long-term treatment outcomes, toxicity and urinary incontinence rates after SRT.Materials and methods: Patients with biochemically recurrent prostate cancer after radical prostatectomy, who were treated with SRT (3D-CRT) at our institution between 1998 and 2012, were included in this retrospective cohort analysis. Primary endpoint was urinary incontinence rate. Secondary endpoints were acute and late grade >= 2 genitourinary (GU) and gastrointestinal (GI) toxicity rates, biochemical progression-free survival (bPFS), distant metastasis-free survival (DMFS), disease specific survival (DSS), and overall survival (OS).Results: 244 patients were included. Median follow-up after SRT was 50 months (range: 4-187 months). Before start of SRT 69.7% of patients were continent for urine. After SRT de novo urinary incontinence complaints (grade >= 1) occurred in the respective acute and late phase in 6.1% and 17.6% of patients. Respective acute grade >= 2 GU and GI toxicity was 19.2% and 17.6%. Late grade >= 2 toxicity for GU was 29.9% and for GI was 21.3%, respectively. The respective 5-year bPFS, OS, DSS and DMFS rates were 47.6%, 91.8%, 98.8% and 80.5%.Conclusions: Experience at our institution with SRT demonstrates that this results in good long-term biochemical control. However, toxicity and urinary incontinence rates were high. (C) 2018 The Authors. Published by Elsevier B.V.
AB - Purpose: For patients with local recurrent disease after radical prostatectomy (35-54%) salvage radiotherapy (SRT) is the treatment of choice. In the post prostatectomy setting, SRT may impose risk at increased toxicity. As data on long-term toxicity, especially on urinary incontinence, are scarce, we report on the long-term treatment outcomes, toxicity and urinary incontinence rates after SRT.Materials and methods: Patients with biochemically recurrent prostate cancer after radical prostatectomy, who were treated with SRT (3D-CRT) at our institution between 1998 and 2012, were included in this retrospective cohort analysis. Primary endpoint was urinary incontinence rate. Secondary endpoints were acute and late grade >= 2 genitourinary (GU) and gastrointestinal (GI) toxicity rates, biochemical progression-free survival (bPFS), distant metastasis-free survival (DMFS), disease specific survival (DSS), and overall survival (OS).Results: 244 patients were included. Median follow-up after SRT was 50 months (range: 4-187 months). Before start of SRT 69.7% of patients were continent for urine. After SRT de novo urinary incontinence complaints (grade >= 1) occurred in the respective acute and late phase in 6.1% and 17.6% of patients. Respective acute grade >= 2 GU and GI toxicity was 19.2% and 17.6%. Late grade >= 2 toxicity for GU was 29.9% and for GI was 21.3%, respectively. The respective 5-year bPFS, OS, DSS and DMFS rates were 47.6%, 91.8%, 98.8% and 80.5%.Conclusions: Experience at our institution with SRT demonstrates that this results in good long-term biochemical control. However, toxicity and urinary incontinence rates were high. (C) 2018 The Authors. Published by Elsevier B.V.
KW - Radiotherapy
KW - Salvage therapy
KW - Toxicity
KW - Urinary incontinence
KW - Prostatic neoplasms
KW - CONVENTIONALLY FRACTIONATED RADIOTHERAPY
KW - RADIATION-THERAPY
KW - NON-INFERIORITY
KW - CANCER
KW - ADJUVANT
KW - PROGRESSION
KW - RECURRENCE
KW - ANTIGEN
KW - PSA
U2 - 10.1016/j.ctro.2018.05.001
DO - 10.1016/j.ctro.2018.05.001
M3 - Article
SN - 2405-6308
VL - 11
SP - 26
EP - 32
JO - Clinical and Translational Radiation Oncology
JF - Clinical and Translational Radiation Oncology
ER -