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RECRUITING
NCT06397703
PHASE2

ADT and SBRT vs SBRT Alone for Unfavorable Intermediate Risk Prostate Cancer

Sponsor: NYU Langone Health

View on ClinicalTrials.gov

Summary

For this study, unfavorable intermediate risk prostate cancer patients will select whether they are to be treated with the standard of care (SOC) 6 months of Androgen Deprivation Therapy (ADT) in conjunction with stereotactic body radiation therapy/radiosurgery (SBRT) directed to the prostate versus SBRT alone. The patient population will include those with National Comprehensive Cancer Network (NCCN)-defined unfavorable intermediate risk disease. All patients will be followed every 6 months for up to 5 years from the first patient treated and will undergo a routine 24-30 months post-SBRT prostate biopsy to assess for local tumor control.

Official title: A Phase II Prospective 2-Arm Cohort Interventional Trial Utilizing Ultra-Hypofractionated SBRT With or Without Short Course Androgen Deprivation Therapy For Unfavorable Intermediate Risk Prostate Cancer

Key Details

Gender

MALE

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

392

Start Date

2024-04-16

Completion Date

2031-04-16

Last Updated

2026-01-28

Healthy Volunteers

No

Conditions

Interventions

DRUG

Leuprolide, Degarelix or Relugolix

Patients assigned to the androgen deprivation therapy (ADT) arm will be treated with monthly Degarelix, or Leuprolide injections or daily Relugolix pills which are all standard ADT interventions.

RADIATION

Stereotactic body radiation therapy/radiosurgery (SBRT)

SBRT will be directed to the prostate and delivered with a prescription dose of 40 Gy in 5 fractions prescribed to the 95% isodose line encompassing the planning target volume. Intra-fraction motion targeting and target position corrections will be utilized for each of the 5 treatment fractions.

Locations (1)

NYU Langone Health

New York, New York, United States