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...
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.

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;

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

• ECOG performance status between 0 and 2;

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

• IPSS score must be ≤ 19 (alpha blockers allowed);

Locations
Other Locations
Italy
Radiation Oncology, ASST Monza (University of Milan Bicocca)
RECRUITING
Monza
Contact Information
Primary
STEFANO ARCANGELI, MD
stefano.arcangeli@unimib.it
+39 039-2333663
Time Frame
Start Date: 2021-04-15
Estimated Completion Date: 2029-04-01
Participants
Target number of participants: 30
Related Therapeutic Areas
Sponsors
Leads: University of Milano Bicocca

This content was sourced from clinicaltrials.gov