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NCT02470897 · OUTCOME

Change in American Urological Association Symptom Score (AUASS)

Stereotactic Body Radiation Therapy With Boost Using Urethral-Sparing Intensity-Modulated Radiation Therapy Planning in Treating Patients With Prostate Cancer · Source last updated 2026-10-13

Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.

Measure
MEAN
Unit
score on a scale
Interval / dispersion
Standard Deviation
Time frame
at Baseline, 1 year, and 2 years

What was measured

The AUASS has a total possible range of scores of 0-35 where 1-7 is considered mild symptoms, 8-19 is considered moderate symptoms, and 20-35 is considered severe symptoms. Questionnaires will be performed prior to treatment, and one and two years after completion of treatment.

Analysis population: Inadequate survey completion at specific time points

Groups in this outcome

Arm A (Moderate Dose SBRT With SIB)

Patients undergo 5 fractions of moderate dose SBRT with SIB every other day for 10 days following urethral-sparing IMRT planning. SBRT: 8.0Gy escalated dose Radiation Therapy Treatment Planning and Simulation: Undergo urethral-sparing IMRT planning SBRT: Undergo moderate dose SBRT with SIB

Arm B (Uniform Dose SBRT)

Patients undergo 5 fractions of uniform dose SBRT every other day for 10 days following urethral-sparing IMRT planning. SBRT: 7.5Gy conventional dose Radiation Therapy Treatment Planning and Simulation: Undergo urethral-sparing IMRT planning SBRT: Undergo uniform dose SBRT

Group identifiers and denominators belong to this outcome only. They may differ in another outcome or in safety reporting.

Analysis denominator · Participants

GroupSource count
Arm A (Moderate Dose SBRT With SIB)100
Arm B (Uniform Dose SBRT)15

Reported measurements

baseline

Analysis denominator · Participants

GroupSource count
Arm A (Moderate Dose SBRT With SIB)100
Arm B (Uniform Dose SBRT)13
Values in score on a scale · Interval/dispersion: Standard Deviation
GroupValueSpreadLowerUpperComment
Arm A (Moderate Dose SBRT With SIB)7.425.05Not reportedNot reportedNot reported
Arm B (Uniform Dose SBRT)7.314.50Not reportedNot reportedNot reported
1 year

Analysis denominator · Participants

GroupSource count
Arm A (Moderate Dose SBRT With SIB)92
Arm B (Uniform Dose SBRT)15
Values in score on a scale · Interval/dispersion: Standard Deviation
GroupValueSpreadLowerUpperComment
Arm A (Moderate Dose SBRT With SIB)8.645.61Not reportedNot reportedNot reported
Arm B (Uniform Dose SBRT)7.675.04Not reportedNot reportedNot reported
2 years

Analysis denominator · Participants

GroupSource count
Arm A (Moderate Dose SBRT With SIB)93
Arm B (Uniform Dose SBRT)11
Values in score on a scale · Interval/dispersion: Standard Deviation
GroupValueSpreadLowerUpperComment
Arm A (Moderate Dose SBRT With SIB)7.105.40Not reportedNot reportedNot reported
Arm B (Uniform Dose SBRT)85.72Not reportedNot reportedNot reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        spread
        5.05
        value
        7.42
      2. group Id
        OG001
        spread
        4.50
        value
        7.31
    denoms
    1. counts
      1. group Id
        OG000
        value
        100
      2. group Id
        OG001
        value
        13
      units
      Participants
    title
    baseline
  2. categories
    1. measurements
      1. group Id
        OG000
        spread
        5.61
        value
        8.64
      2. group Id
        OG001
        spread
        5.04
        value
        7.67
    denoms
    1. counts
      1. group Id
        OG000
        value
        92
      2. group Id
        OG001
        value
        15
      units
      Participants
    title
    1 year
  3. categories
    1. measurements
      1. group Id
        OG000
        spread
        5.40
        value
        7.10
      2. group Id
        OG001
        spread
        5.72
        value
        8
    denoms
    1. counts
      1. group Id
        OG000
        value
        93
      2. group Id
        OG001
        value
        11
      units
      Participants
    title
    2 years
denoms
  1. counts
    1. group Id
      OG000
      value
      100
    2. group Id
      OG001
      value
      15
    units
    Participants
description
The AUASS has a total possible range of scores of 0-35 where 1-7 is considered mild symptoms, 8-19 is considered moderate symptoms, and 20-35 is considered severe symptoms. Questionnaires will be performed prior to treatment, and one and two years after completion of treatment.
dispersion Type
Standard Deviation
groups
  1. description
    Patients undergo 5 fractions of moderate dose SBRT with SIB every other day for 10 days following urethral-sparing IMRT planning. SBRT: 8.0Gy escalated dose Radiation Therapy Treatment Planning and Simulation: Undergo urethral-sparing IMRT planning SBRT: Undergo moderate dose SBRT with SIB
    id
    OG000
    title
    Arm A (Moderate Dose SBRT With SIB)
  2. description
    Patients undergo 5 fractions of uniform dose SBRT every other day for 10 days following urethral-sparing IMRT planning. SBRT: 7.5Gy conventional dose Radiation Therapy Treatment Planning and Simulation: Undergo urethral-sparing IMRT planning SBRT: Undergo uniform dose SBRT
    id
    OG001
    title
    Arm B (Uniform Dose SBRT)
param Type
MEAN
population Description
Inadequate survey completion at specific time points
reporting Status
POSTED
time Frame
at Baseline, 1 year, and 2 years
title
Change in American Urological Association Symptom Score (AUASS)
type
SECONDARY
unit Of Measure
score on a scale

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Preserved source evidence · Not medical advice