Long-term urinary continence and influencing factors after salvage radiotherapy: results of the SAKK 09/10 dose escalation trial

•32.2 % of patients in the overall cohort had baseline incontinence (8.7 % ≥G2)•51.9 % of the initially continent (<G1) patients remained continent.•54.1 % of the initially incontinent patients (≥G1) showed an improvement.•Nerve sparing technique was associated with less UI in multivariate analys...

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Published inRadiotherapy and oncology Vol. 211; p. 111040
Main Authors Schröder, Christina, Zwahlen, Daniel R., Schär, Sämi, Hölscher, Tobias, Arnold, Winfried, Polat, Bülent, Hildebrandt, Guido, Müller, Arndt-Christian, Putora, Paul Martin, Papachristofilou, Alexandros, Schär, Corinne, Hayoz, Stefanie, Sumila, Marcin, Zaugg, Kathrin, Guckenberger, Matthias, Ost, Piet, Bosetti, Davide Giovanni, Reuter, Christiane, Gomez, Silvia, Khanfir, Kaouthar, Beck, Marcus, Riesterer, Oliver, Thalmann, George N., Aebersold, Daniel M., Ghadjar, Pirus
Format Journal Article
LanguageEnglish
Published Ireland Elsevier B.V 01.10.2025
Subjects
Online AccessGet full text
ISSN0167-8140
1879-0887
1879-0887
DOI10.1016/j.radonc.2025.111040

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Abstract •32.2 % of patients in the overall cohort had baseline incontinence (8.7 % ≥G2)•51.9 % of the initially continent (<G1) patients remained continent.•54.1 % of the initially incontinent patients (≥G1) showed an improvement.•Nerve sparing technique was associated with less UI in multivariate analysis.•Increase in urinary function symptom scale from 15.9 (baseline) to 22.9 (60 months) This study aimed to investigate late urinary incontinence (UI) after salvage radiotherapy (sRT) and the effect of dose escalation on late UI, incontinence recovery, and quality of life (QoL) as part of the SAKK 09/10 phase III trial. The SAKK 09/10 trial was a multicenter, randomized, controlled trial for prostate cancer patients receiving sRT. Eligible patients were randomized to receive either conventional (64 Gy) or dose-escalated (70 Gy) sRT. Baseline and follow-up data were collected on urinary incontinence related QoL, and treatment toxicity. 344 evaluable patients were analyzed. Baseline incontinence (≥Grade (G)1) was reported in 32.2 % of patients, with 8.7 % having ≥ G2. During follow-up (median 6.2 years), 47.2 % of the initially continent (<G1) patients showed a statistically significant (p < 0.001) decline in continence with no significant difference between the treatment groups (p = 0.17). Of the initially incontinent patients, 54.1 % showed an improvement whilst 16.2 % showed further decline. 29.7 % had stable UI. There was no significant difference between the treatment arms (p = 0.36). In multivariable logistic regression, nerve sparing technique was associated with less UI at 24 months (p = 0.029) and at 60 months age (p = 0.031) and resection status (p = 0.046) were significant. There was a steady worsening of urinary symptoms reported over 60 months post RT, with an increase in the symptom scales from a mean of 15.9 at baseline to 22.9 at 60 months. More than half of the patients that were continent at baseline remained continent during follow up while incontinent patients showed a variable course. UI was not different between the RT treatment arms.
AbstractList This study aimed to investigate late urinary incontinence (UI) after salvage radiotherapy (sRT) and the effect of dose escalation on late UI, incontinence recovery, and quality of life (QoL) as part of the SAKK 09/10 phase III trial.PURPOSEThis study aimed to investigate late urinary incontinence (UI) after salvage radiotherapy (sRT) and the effect of dose escalation on late UI, incontinence recovery, and quality of life (QoL) as part of the SAKK 09/10 phase III trial.The SAKK 09/10 trial was a multicenter, randomized, controlled trial for prostate cancer patients receiving sRT. Eligible patients were randomized to receive either conventional (64 Gy) or dose-escalated (70 Gy) sRT. Baseline and follow-up data were collected on urinary incontinence related QoL, and treatment toxicity.METHODSThe SAKK 09/10 trial was a multicenter, randomized, controlled trial for prostate cancer patients receiving sRT. Eligible patients were randomized to receive either conventional (64 Gy) or dose-escalated (70 Gy) sRT. Baseline and follow-up data were collected on urinary incontinence related QoL, and treatment toxicity.344 evaluable patients were analyzed. Baseline incontinence (≥Grade (G)1) was reported in 32.2 % of patients, with 8.7 % having ≥ G2. During follow-up (median 6.2 years), 47.2 % of the initially continent (<G1) patients showed a statistically significant (p < 0.001) decline in continence with no significant difference between the treatment groups (p = 0.17). Of the initially incontinent patients, 54.1 % showed an improvement whilst 16.2 % showed further decline. 29.7 % had stable UI. There was no significant difference between the treatment arms (p = 0.36). In multivariable logistic regression, nerve sparing technique was associated with less UI at 24 months (p = 0.029) and at 60 months age (p = 0.031) and resection status (p = 0.046) were significant. There was a steady worsening of urinary symptoms reported over 60 months post RT, with an increase in the symptom scales from a mean of 15.9 at baseline to 22.9 at 60 months.RESULTS344 evaluable patients were analyzed. Baseline incontinence (≥Grade (G)1) was reported in 32.2 % of patients, with 8.7 % having ≥ G2. During follow-up (median 6.2 years), 47.2 % of the initially continent (<G1) patients showed a statistically significant (p < 0.001) decline in continence with no significant difference between the treatment groups (p = 0.17). Of the initially incontinent patients, 54.1 % showed an improvement whilst 16.2 % showed further decline. 29.7 % had stable UI. There was no significant difference between the treatment arms (p = 0.36). In multivariable logistic regression, nerve sparing technique was associated with less UI at 24 months (p = 0.029) and at 60 months age (p = 0.031) and resection status (p = 0.046) were significant. There was a steady worsening of urinary symptoms reported over 60 months post RT, with an increase in the symptom scales from a mean of 15.9 at baseline to 22.9 at 60 months.More than half of the patients that were continent at baseline remained continent during follow up while incontinent patients showed a variable course. UI was not different between the RT treatment arms.CONCLUSIONMore than half of the patients that were continent at baseline remained continent during follow up while incontinent patients showed a variable course. UI was not different between the RT treatment arms.
•32.2 % of patients in the overall cohort had baseline incontinence (8.7 % ≥G2)•51.9 % of the initially continent (<G1) patients remained continent.•54.1 % of the initially incontinent patients (≥G1) showed an improvement.•Nerve sparing technique was associated with less UI in multivariate analysis.•Increase in urinary function symptom scale from 15.9 (baseline) to 22.9 (60 months) This study aimed to investigate late urinary incontinence (UI) after salvage radiotherapy (sRT) and the effect of dose escalation on late UI, incontinence recovery, and quality of life (QoL) as part of the SAKK 09/10 phase III trial. The SAKK 09/10 trial was a multicenter, randomized, controlled trial for prostate cancer patients receiving sRT. Eligible patients were randomized to receive either conventional (64 Gy) or dose-escalated (70 Gy) sRT. Baseline and follow-up data were collected on urinary incontinence related QoL, and treatment toxicity. 344 evaluable patients were analyzed. Baseline incontinence (≥Grade (G)1) was reported in 32.2 % of patients, with 8.7 % having ≥ G2. During follow-up (median 6.2 years), 47.2 % of the initially continent (<G1) patients showed a statistically significant (p < 0.001) decline in continence with no significant difference between the treatment groups (p = 0.17). Of the initially incontinent patients, 54.1 % showed an improvement whilst 16.2 % showed further decline. 29.7 % had stable UI. There was no significant difference between the treatment arms (p = 0.36). In multivariable logistic regression, nerve sparing technique was associated with less UI at 24 months (p = 0.029) and at 60 months age (p = 0.031) and resection status (p = 0.046) were significant. There was a steady worsening of urinary symptoms reported over 60 months post RT, with an increase in the symptom scales from a mean of 15.9 at baseline to 22.9 at 60 months. More than half of the patients that were continent at baseline remained continent during follow up while incontinent patients showed a variable course. UI was not different between the RT treatment arms.
Highlights•32.2 % of patients in the overall cohort had baseline incontinence (8.7 % ≥G2) •51.9 % of the initially continent (<G1) patients remained continent. •54.1 % of the initially incontinent patients (≥G1) showed an improvement. •Nerve sparing technique was associated with less UI in multivariate analysis. •Increase in urinary function symptom scale from 15.9 (baseline) to 22.9 (60 months)
This study aimed to investigate late urinary incontinence (UI) after salvage radiotherapy (sRT) and the effect of dose escalation on late UI, incontinence recovery, and quality of life (QoL) as part of the SAKK 09/10 phase III trial. The SAKK 09/10 trial was a multicenter, randomized, controlled trial for prostate cancer patients receiving sRT. Eligible patients were randomized to receive either conventional (64 Gy) or dose-escalated (70 Gy) sRT. Baseline and follow-up data were collected on urinary incontinence related QoL, and treatment toxicity. 344 evaluable patients were analyzed. Baseline incontinence (≥Grade (G)1) was reported in 32.2 % of patients, with 8.7 % having ≥ G2. During follow-up (median 6.2 years), 47.2 % of the initially continent (<G1) patients showed a statistically significant (p < 0.001) decline in continence with no significant difference between the treatment groups (p = 0.17). Of the initially incontinent patients, 54.1 % showed an improvement whilst 16.2 % showed further decline. 29.7 % had stable UI. There was no significant difference between the treatment arms (p = 0.36). In multivariable logistic regression, nerve sparing technique was associated with less UI at 24 months (p = 0.029) and at 60 months age (p = 0.031) and resection status (p = 0.046) were significant. There was a steady worsening of urinary symptoms reported over 60 months post RT, with an increase in the symptom scales from a mean of 15.9 at baseline to 22.9 at 60 months. More than half of the patients that were continent at baseline remained continent during follow up while incontinent patients showed a variable course. UI was not different between the RT treatment arms.
ArticleNumber 111040
Author Sumila, Marcin
Bosetti, Davide Giovanni
Ghadjar, Pirus
Gomez, Silvia
Khanfir, Kaouthar
Guckenberger, Matthias
Aebersold, Daniel M.
Thalmann, George N.
Putora, Paul Martin
Papachristofilou, Alexandros
Hayoz, Stefanie
Zaugg, Kathrin
Schär, Corinne
Hildebrandt, Guido
Reuter, Christiane
Riesterer, Oliver
Schär, Sämi
Zwahlen, Daniel R.
Arnold, Winfried
Schröder, Christina
Beck, Marcus
Hölscher, Tobias
Müller, Arndt-Christian
Polat, Bülent
Ost, Piet
Author_xml – sequence: 1
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  organization: Department of Radiation Oncology, Kantonsspital Winterthur, Winterthur, Switzerland
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  givenname: Daniel R.
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  surname: Zwahlen
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  organization: Department of Radiation Oncology, Kantonsspital Winterthur, Winterthur, Switzerland
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  givenname: Sämi
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  surname: Schär
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  givenname: Tobias
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  surname: Hölscher
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  organization: Department of Radiotherapy and Radiation Oncology, Faculty of Medicine and University Hospital Carl Gustav Carus, TUD Dresden University of Technology, Dresden, Germany
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  givenname: Winfried
  surname: Arnold
  fullname: Arnold, Winfried
  organization: Department of Radiation Oncology, Kantonsspital Luzern, Lucerne, Switzerland
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  givenname: Bülent
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  surname: Müller
  fullname: Müller, Arndt-Christian
  organization: Department of Radiation Oncology, University Hospital Tübingen, Tübingen, Germany
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  givenname: Paul Martin
  surname: Putora
  fullname: Putora, Paul Martin
  organization: Department of Radiation Oncology, Inselspital, Bern University Hospital, and Bern University, Bern, Switzerland
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  givenname: Alexandros
  orcidid: 0000-0001-5619-747X
  surname: Papachristofilou
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  organization: Department of Radiation Oncology, University Hospital Basel, Basel, Switzerland
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  givenname: Corinne
  surname: Schär
  fullname: Schär, Corinne
  organization: Swiss Group for Clinical Cancer Research Competence Center, Bern, Switzerland
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  givenname: Stefanie
  orcidid: 0000-0002-2265-6559
  surname: Hayoz
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  givenname: Marcin
  surname: Sumila
  fullname: Sumila, Marcin
  organization: Department of Radiation Oncology, Hirslanden Hospital Group, Zurich, Switzerland
– sequence: 14
  givenname: Kathrin
  surname: Zaugg
  fullname: Zaugg, Kathrin
  organization: Department of Radiation Oncology, Stadtspital Triemli, Zurich, Switzerland
– sequence: 15
  givenname: Matthias
  orcidid: 0000-0002-7146-9071
  surname: Guckenberger
  fullname: Guckenberger, Matthias
  organization: Department of Radiation Oncology, University Hospital Zurich, Zurich, Switzerland
– sequence: 16
  givenname: Piet
  orcidid: 0000-0002-2203-4848
  surname: Ost
  fullname: Ost, Piet
  organization: Department of Radiation Oncology, Ghent University Hospital, Ghent, Belgium
– sequence: 17
  givenname: Davide Giovanni
  orcidid: 0000-0002-2654-1281
  surname: Bosetti
  fullname: Bosetti, Davide Giovanni
  organization: Department of Radiation Oncology, Oncology Institute of Southern Switzerland (IOSI), EOC, Bellinzona, Switzerland
– sequence: 18
  givenname: Christiane
  surname: Reuter
  fullname: Reuter, Christiane
  organization: Department of Radiation Oncology, Kantonsspital Münsterlingen, Münsterlingen, Switzerland
– sequence: 19
  givenname: Silvia
  orcidid: 0009-0002-7236-7269
  surname: Gomez
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  givenname: Kaouthar
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  givenname: Oliver
  orcidid: 0000-0002-9508-0546
  surname: Riesterer
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– sequence: 23
  givenname: George N.
  surname: Thalmann
  fullname: Thalmann, George N.
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– sequence: 24
  givenname: Daniel M.
  surname: Aebersold
  fullname: Aebersold, Daniel M.
  organization: Department of Radiation Oncology, Inselspital, Bern University Hospital, and Bern University, Bern, Switzerland
– sequence: 25
  givenname: Pirus
  surname: Ghadjar
  fullname: Ghadjar, Pirus
  organization: Department of Radiation Oncology, Inselspital, Bern University Hospital, and Bern University, Bern, Switzerland
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Keywords Urinary incontinence
Radiotherapy
Prostate cancer
Quality of life
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Snippet •32.2 % of patients in the overall cohort had baseline incontinence (8.7 % ≥G2)•51.9 % of the initially continent (<G1) patients remained continent.•54.1 % of...
Highlights•32.2 % of patients in the overall cohort had baseline incontinence (8.7 % ≥G2) •51.9 % of the initially continent (<G1) patients remained continent....
This study aimed to investigate late urinary incontinence (UI) after salvage radiotherapy (sRT) and the effect of dose escalation on late UI, incontinence...
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SubjectTerms Hematology, Oncology, and Palliative Medicine
Prostate cancer
Quality of life
Radiotherapy
Urinary incontinence
Title Long-term urinary continence and influencing factors after salvage radiotherapy: results of the SAKK 09/10 dose escalation trial
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