The purpose of this study is to observe PSA response and incidence of side effects in patients diagnosed with intermediate to high risk prostate cancer and treated with Cesium-131 in combination of external beam therapy.
Study Type
OBSERVATIONAL
Arizona Oncology Services Foundation
Phoenix, Arizona, United States
Eisenhower Medical Center
Rancho Mirage, California, United States
Dorthory Schneider Cancer Center
San Mateo, California, United States
The analysis of dosimetric data resultant from Cs-131 permanent prostate brachytherapy in combination with external beam radiation therapy in the setting of intermediate to high risk cancer of the prostate.
Data collected for analysis will be total therapeutic dose delivered to the prostate by the Cs-131 brachytherapy implant treatment in units of Gy.
Time frame: 5 years
The analysis of treatment related morbidities following Cs-131 prostate brachytherapy in combination with external beam therapy for intermediate to high risk cancer of the prostate.
Data collected for analysis will be the EPIC prostate cancer quality of life questionnaire.
Time frame: 5 years
The analysis of PSA control rates following Cs-131 prostate brachytherapy in combination with external beam therapy for intermediate to high risk cancer of the prostate.
Data collected for analysis will be PSA measurements.
Time frame: 5 years
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Levine Cancer Center
Worcester, Massachusetts, United States
St. Mary's Regional Medical Center
Reno, Nevada, United States
Northshore Medical Accelerator
Smithtown, New York, United States
Sentara Cancer Institute
Hampton, Virginia, United States
Virginia Mason Medical Center
Seattle, Washington, United States
Seattle Prostate Institute / Swedish Hospital
Seattle, Washington, United States