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NCT06369246RecruitingPhase 2

PRORAD-5 PROstate RADiation in 5 Fractions: Phase II Five Fraction Radiotherapy for Patients With Advanced Prostate Cancer.

Source: ClinicalTrials.gov · Last updated 21 Aug 2026

Brief summary (registry, in English)

To look at the safety and effectiveness of stereotactic body radiation therapy (SBRT) in treating advanced or high-risk prostate cancer.

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
100 (estimated)
First submitted
12 Apr 2024
Start date
Jun 2024
Primary completion date
Sept 2027
Lead sponsor
M.D. Anderson Cancer Center
NCT number
NCT06369246

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 100
  • From Jun 2024 to the primary completion date, Sept 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior prostatectomy, cryosurgery, or HIFU for adenocarcinoma of the prostate
  • Prior radiotherapy to the region of the study cancer that would result in overlap of radiation fields

Other illness

  • Diagnosis of active scleroderma, lupus, or other rheumatologic disease which in the opinion of the treating radiation oncologist precludes safe RT.
  • Distant metastatic disease on conventional imaging, which by the discretion of the treating physician cannot be treated definitively.

Who the study is looking for

  • Pathologically (histologically or cytologically) proven diagnosis of adenocarcinoma of prostate within one year of study entry. Evaluation can happen outside of MD Anderson as long as histological confirmation takes place at MD Anderson.
    • cT1c-T3a by digital exam or imaging (AJCC 8th Ed.). No cT3b-4 by digital exam or imaging (AJCC 8th Ed.)
    • Gleason Grade Group 2-5 (Gleason 7, 8, 9, 10).
    • If Gleason Grade 2, must meet definition of unfavorable intermediate risk (at least one of the following: cT2b, and/or ≥ 50% biopsy cores positive, and/or PSA \>10 ng/mL prior to starting androgen deprivation therapy (ADT).
    • If a participant is taking 5-alpha reductase inhibitors the measured PSA may be doubled).
  • Node negative by conventional imaging.
  • Be ≥ 18 years of age on the day of signing informed consent.
  • Prior pharmacologic androgen ablation for prostate cancer is allowed only if the onset of androgen ablation (both LHRH agonist and oral anti-androgen) is ≤ 185 days prior to registration; Please note: baseline PSA must be obtained prior to the start of any ADT.
  • ECOG performance status 0-2.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
MD Anderson Cancer Center
Coordinator of this site? Confirm its status
HoustonUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.