Moderate Hypofractionated Boost to the Prostate With Pelvic RT in High Risk Prostate Cancer

Status: Recruiting
Location: See location...
Intervention Type: Radiation
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This is a single-arm phase II prospective trials that is recruiting 100 participants. The study population that is being investigated are patients with localized high-risk or node-positive prostate cancer. Participants will receive external beam radiotherapy as a moderately hypofractionated boost to the prostate with pelvic radiation therapy. Androgen deprivation therapy will be prescribed at the discretion of the treating physician as per standard of care.

Eligibility
Participation Requirements
Sex: Male
Minimum Age: 18
Healthy Volunteers: f
View:

• Age \> 18 years.

• Able to provide informed consent.

• Histologic diagnosis of prostate adenocarcinoma.

• ECOG performance status 0-1.

• High-risk localized disease by NCCN criteria (\>cT3, Grade group \>4, or PSA \>20 ng/mL) or clinical N1 disease.

• Clinical M0 by conventional imaging (computed tomography (CT) and bone scan (BS)) and/or molecular imaging (prostate specific membrane antigen (PSMA)- positron emission tomography (PET))

Locations
Other Locations
Canada
Princess Margaret Cancer Center
RECRUITING
Toronto
Contact Information
Primary
Rachel Glicksman, MD
rachel.glicksman@rmp.uhn.ca
416-946-4486
Time Frame
Start Date: 2022-07-18
Estimated Completion Date: 2030-07
Participants
Target number of participants: 100
Treatments
Experimental: Moderate Hypofracitonated Boost to the Prostate with Pelvic Radiation Therapy
External beam radiotherapy- 60 Gy in 20 fractions to the prostate, 48 Gy in 20 fractions to the pelvis, 68 Gy in 20 fraction optional boost to prostatic dominant intraprostatic lesion, 55 Gy in 20 fraction optional boost to involved pelvic lymph nodes
Related Therapeutic Areas
Sponsors
Leads: University Health Network, Toronto

This content was sourced from clinicaltrials.gov