Quality of Life in Patients With Clinically Localized Prostate Cancer Treated With Radiosurgery

Clinicaltrials.gov ID: NCT01766492
db-list-check Status RECRUITING
b-loader Phase
b-people Age 18 - 99 Years
b-bullseye-arrow Enrollments 200

Conditions

Prostate Cancer, Localized Malignant Neoplasm

Summary

Quality of life data following SBRT for prostate cancer has been obtained in only a small numbers of patients. A prospective study using validated quality of life questionnaires is needed to determine outcomes after treatment with SBRT. Our study will be the first essential step in developing a better evidence base on the comparative risks and benefits of SBRT treatment with regards to quality of life assessment and outcomes.

Detailed Description

Study Design (for example, hypothesis, research question, standard and experimental procedures, special or unusual equipment or procedures):

The main goal of this study is to evaluate quality of life outcomes and changes in patient reported symptoms (e.g. urinary, bowel and sexual function) in patients receiving SBRT treatment for clinically localized prostate cancer. Validated quality of life questionnaires will be administered in a deidentified, prospective fashion. Eligible subjects will be patients undergoing SBRT treatment for prostate cancer.

Hypothesis: Patients undergoing SBRT will have similar cancer control and symptoms as men who are treated with other radiation therapy modalities.

Primary objective: To evaluate quality of life outcomes (e.g. fatigue, urinary, bowel and sexual function) for patients with clinically localized prostate cancer treated with SBRT.

Secondary objectives: Prospective data on cancer control and toxicity following SBRT for clinically localized prostate cancer.

Locations

1 location Found with status Recruiting

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Sean P Collins, MD, PhD

Eligibility Criteria

Inclusion Criteria:

* Histologically confirmed adenocarcinoma of prostate
* Signed study-specific consent
* Prostate Specific Antigen (PSA) within 60 days of registration

Exclusion Criteria:

* Prior pelvic radiotherapy
* Prior radical prostate surgery
* Medical or psychiatric illness that would interfere with treatment or follow up
* Implanted hardware adjacent to the prostate that would prohibit appropriate treatment planning and/or treatment delivery

Study Plan

male (age > 18 y/o) with prostate cancer

Men received Stereotactic Body Radiation Therapy (SBRT) for clinically localized prostate cancer

  • RADIATION:

    Stereotactic Body Radiation Therapy (SBRT)

    Description:

    Stereotactic body radiation therapy for prostate

Outcome Measures

Primary Outcome Measures

fatigue

Time Frame: 2 years

urinary symptoms

Time Frame: 24 months

bowel symptoms

Time Frame: 24 months

sexual function

Time Frame: 24 months

Secondary Outcome Measures

cancer control

Time Frame: 24 months

toxicity symptoms

Time Frame: 24 months

Timeline

  • Last Updated
    February 23, 2023
  • Start Date
    January 11, 2013
  • Today
    February 5, 2025
  • Completion Date ( Estimated )
    April 1, 2025

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