RecruitingNot ApplicableNCT06995053

Computed Tomography-Guided Stereotactic Body Radiation Therapy With Intrafraction Motion Monitoring for the Treatment of Localized Prostate Cancer, ILLUSION Trial

Image-Guidance With Triggered Beam Hold To Implanted Fiducial Markers or Hypersight for Stereotactic Body Radiotherapy for Prostate Cancer (ILLUSION)


Sponsor

Jonsson Comprehensive Cancer Center

Enrollment

80 participants

Start Date

Jun 27, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This clinical trial studies the side effects of computed tomography (CT)-guided stereotactic body radiation therapy (SBRT) with intrafraction motion monitoring and to see how well it works in treating patients with prostate cancer that has not spread to other parts of the body (localized). In CT-guided SBRT, x-ray-based imaging and cone-beam CTs are used to define and localize the area to be treated with SBRT. SBRT is a type of external radiation therapy that uses special equipment to position a patient and precisely deliver radiation to tumors in the body (except the brain). The total dose of radiation is divided into smaller doses given over several days. This type of radiation therapy helps spare normal tissue. A recent randomized trial showed that while SBRT is associated with less urinary incontinence and erectile dysfunction than complete surgical removal of the prostate, there are more urinary irritative side effects and more bowel side effects than with surgery. One source of uncertainty in SBRT that may contribute to genitourinary (GU) and gastrointestinal (GI) side effects is the necessity of treating a "margin" of volume around the prostate to account for its movement during SBRT. Intrafraction motion monitoring is any technique or system designed to track the movement of the body and target during fractions of external beam radiation to keep the beam on target. This allows for the patient to be repositioned, if needed, to ensure delivery of the SBRT to only the planned treatment area. CT-guided SBRT with intrafraction motion monitoring may lower GU and GI side effects by allowing tighter margins, as has been demonstrated with magnetic resonance imaging (MRI)-guided SBRT.


Eligibility

Sex: MALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study tests a focused type of radiation therapy called stereotactic body radiation therapy (SBRT) that tracks the prostate's movement in real time during treatment, so radiation can be aimed more precisely. The goal is to treat localized prostate cancer effectively while reducing side effects. **You may be eligible if...** - You are 18 or older with biopsy-confirmed prostate cancer that has not spread beyond the prostate or nearby lymph nodes - Imaging shows no evidence of cancer in bones or organs - Your cancer has been staged using NCCN guidelines **You may NOT be eligible if...** - Your prostate cancer is of an aggressive rare type (neuroendocrine or small cell) - You have distant metastases - You have previously had whole-gland prostate treatment (cryosurgery, HIFU, or brachytherapy) - You have had prior pelvic radiation - You have Crohn's disease, ulcerative colitis, or a rare condition called ataxia telangiectasia Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDUREBiospecimen Collection

Undergo blood sample collection

PROCEDUREComputed Tomography

Undergo CT

RADIATIONCT-guided Stereotactic Body Radiation Therapy

Undergo CT-guided SBRT with intrafraction motion monitoring

OTHERIntrafraction Motion Monitoring

Undergo CT-guided SBRT with intrafraction motion monitoring

PROCEDUREMagnetic Resonance Imaging

Undergo MRI

OTHERQuestionnaire Administration

Ancillary studies


Locations(1)

UCLA / Jonsson Comprehensive Cancer Center

Los Angeles, California, United States

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NCT06995053


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