Adaptive Stereotactic Body Radiation Therapy to the Prostate and Pelvic Nodes With Simultaneous Integrated Boost to the MR-detected Nodule for Patients With High-risk and Unfavorable Intermediate-risk Prostate Cancer

NAActive, not recruitingINTERVENTIONAL
Enrollment

28

Participants

Timeline

Start Date

January 18, 2023

Primary Completion Date

October 25, 2025

Study Completion Date

July 25, 2030

Conditions
Prostate CancerCancer of the Prostate
Interventions
DEVICE

Ethos Varian treatment system

Device that will be used to administer radiotherapy

RADIATION

Adaptive stereotactic body radiotherapy

Radiotherapy interruptions are acceptable as long as treatments are no more than 16 days apart.

DRUG

Androgen deprivation therapy

"Androgen deprivation therapy (ADT) will be administered to study patients according to institutional standard. Patients should initiate ADT beginning no sooner than 60 days prior to start of radiation. ADT is defined as a GnRH agonist/antagonist (leuprolide, goserelin, degarelix, or relugolix). Patients treated with leuprolide, goserelin, or degarelix should also receive an androgen receptor antagonist (flutamide or bicalutamide) for 30 days from the start of GnRH agonist/antagonist or until the end of radiation, depending on institutional standard and physician preference.~Agent selection is per treating physician discretion and will be administered per institutional standard and FDA-approved labeling."

Trial Locations (1)

63110

Washington University School of Medicine, St Louis

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Varian Medical Systems

INDUSTRY

lead

Washington University School of Medicine

OTHER

NCT05628363 - Adaptive Stereotactic Body Radiation Therapy to the Prostate and Pelvic Nodes With Simultaneous Integrated Boost to the MR-detected Nodule for Patients With High-risk and Unfavorable Intermediate-risk Prostate Cancer | Biotech Hunter | Biotech Hunter