Prostate Cancer Clinical Trials

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Single-Dose Image-Guided Radiotherapy (IGRT) With Focal Boost to the MRI-defined Macroscopic Tumor Volume for Intermediate Unfavorable and High Risk Prostate Cancer

Status: Recruiting
Location: See location...
Intervention Type: Radiation
Study Type: Observational
SUMMARY

Published clinical evidence confirms that a single dose of 24 Gy provides unprecedented long-term local control in primary and metastatic prostate cancer with safe toxicity profiles, provided that exposure of surrounding healthy tissues is critically assessed with fulfillment of strict constraints and dose distribution is accomplished using image guidance and tracking tools. In the present trial, intermediate unfavorable and selected high-risk organ-confined prostate cancer patients will undergo Single Dose Radiation Therapy (SDRT) With Focal Boost to the MRI-defined Macroscopic Tumor Volume by means of image-guided volumetric intensity-modulated arc radiotherapy (IGRT-VMAT) and state-of-the-art treatment-planning and quality assurance procedures. Androgen Deprivation Therapy (ADT) type and duration has been set as per standard of care, in accordance with current recommendations and guidelines. The results of the study will enable us to find out if the new, shorter treatment (1 doses of radiotherapy), has a similar level of side effects as the 5 dose treatment and is suitable for further study.

Eligibility
Participation Requirements
Sex: Male
Minimum Age: 18
Maximum Age: 90
Healthy Volunteers: f
View:

• Histologically proven prostate adenocarcinoma;

• Intermediate and High risk disease, as per the NCCN definition;

• a PI-RADS 3-5 dominant intraprostatic lesion on multiparametric MRI (mpMRI);

• N0M0 at staging with standard techniques (Bone Scan and Abdominal CT) or (preferably) PSMA PET-CT;

• World Health Organization performance status 0-1;

• Life expectancy of \> 5 years, in the opinion of the investigator;

• IPSS score must be ≤ 15 (alpha blockers allowed);

• Prostate gland volume ≤100 g as estimated by computed tomography (CT), ultrasound, or MRI.

Locations
Other Locations
Italy
Radiation Oncology, Fondazione IRCCS San Gerardo dei Tintori
RECRUITING
Monza
Contact Information
Primary
Stefano Arcangeli, MD
stefano.arcangeli@unimib.it
+39 039 233 3663
Time Frame
Start Date: 2026-01-28
Estimated Completion Date: 2034-07-31
Participants
Target number of participants: 58
Treatments
5 Fx SBRT
Patients will receive 36.25 Gy SBRT in five fractions over two weeks
1 Fx SDRT
Patients will receive 24 Gy SDRT with urethra-sparing and a focal isotoxic GTV boost up to 27 Gy
Related Therapeutic Areas
Sponsors
Leads: University of Milano Bicocca

This content was sourced from clinicaltrials.gov