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Spots Global Cancer Trial Database for LDR vs. HDR Brachytherapy for Prostate Cancer

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Trial Identification

Brief Title: LDR vs. HDR Brachytherapy for Prostate Cancer

Official Title: A Phase III Randomized Study of Low Dose Rate Compared to High Dose Rate Prostate Brachytherapy for Favorable Risk and Low Tier Intermediate Risk Prostate Cancer

Study ID: NCT03426748

Conditions

Prostate Cancer

Study Description

Brief Summary: H17-02904 is a randomized comparison of low dose rate vs. high dose rate prostate brachytherapy for favorable and intermediate risk prostate cancer suitable for brachytherapy as monotherapy. This is a continuation with expanded accrual of the randomized Pilot study H15-02103

Detailed Description: Men suitable for prostate brachytherapy as monotherapy will undergo multiparametric Magnetic Resonance Imaging for staging and identification of a dominant lesion and will be randomly selected for either a single low dose rate permanent seed implant or 2 fractions of high dose rate brachytherapy. Using image registration techniques, dominant lesions will be biopsied under anesthesia at the start of the brachytherapy procedure. Biopsies will reviewed for tumor Gleason score and sent for Cell Cycle Progression testing (Prolaris). Patients receiving high dose rate brachytherapy will also have biopsies between the 2 fractions to assess tumor changes induced from the first fraction. Post implant quality assurance will determine the dose to the dominant lesions and compare these between the 2 types of brachytherapy. Post implant symptoms will be tracked for severity and time course.

Eligibility

Minimum Age: 40 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: MALE

Healthy Volunteers: No

Locations

British Columbia Cancer Agency Center for the Southern Interior, Kelowna, British Columbia, Canada

Contact Details

Name: Ross Halperin, MD

Affiliation: British Columbia Cancer Agency Program Director

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

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