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RECRUITING
NCT02918253
NA

HDR Focal: Feasibility Study

Sponsor: University Health Network, Toronto

View on ClinicalTrials.gov

Summary

Brachytherapy as a monotherapy treatment is highly effective for localized prostate cancer, traditionally being delivered to the whole prostate gland. Lately, low dose rate (LDR) brachytherapy has been increasingly replaced by high dose rate (HDR) brachytherapy treatment schemes. While brachytherapy's oncologic outcomes are excellent, it is not without incidence adverse effects including urinary, rectal, and sexual toxicities that affect the patient's quality of life. This study will incorporate HDR monotherapy treatment option for early stages and favourable risk prostate cancer. Additionally, we aim to evaluate the role of focal HDR brachytherapy for well-defined disease based on multiparametric MRI (mpMRI). This approach may offer an option of reducing the treatment toxicities while maintaining oncologic outcomes when compared with whole-gland therapy. Advantages in quality of life could be exhibited in the form of reduced urinary discomfort and incontinence, rectal symptoms, and improved erectile and prostatic gland function. This study would be particularly relevant in the current era of earlier localized prostate cancer detection, where newer imaging modalities (e.g. mpMRI) become a routine component of patient care.

Official title: HDR Monotherapy for Prostate Cancer: A Feasibility Study of Focal Radiotherapy Yields

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

30

Start Date

2016-10-14

Completion Date

2027-12

Last Updated

2025-03-06

Healthy Volunteers

No

Conditions

Interventions

RADIATION

targeted focal HDR brachytherapy

RADIATION

Whole-gland HDR Brachytherapy

Control/Standard of Care

Locations (1)

Princess Margaret Cancer Centre

Toronto, Ontario, Canada