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RECRUITING
NCT04035642
NA

Phase II Study of Single-Dose Image-Guided Radiotherapy (SDRT) for Prostate Cancer

Sponsor: Fundacao Champalimaud

View on ClinicalTrials.gov

Summary

The present study evaluates clinical outcomes and treatment-related toxicity following definitive ultra-high single dose external beam radiotherapy delivered to patients with low- or intermediate-risk adenocarcinoma of the prostate. Modern computer-driven technology enables the implementation of ultra-high Single-Dose Image-Guided Radiotherapy (SD-IGRT) safely. Prostate cancer patients classified according to the current National Comprehensive Cancer Network (NCCN) guidelines as low or intermediate risk (biopsy Gleason score of ≤7 and/or Prostate Specific Antigen (PSA) level ≤20 ng/mL and/or Stage T1, T2a, T2b or T2c) are eligible for this study. Patients will undergo SD-IGRT with volumetric intensity-modulated arc radiotherapy (VMAT) with state-of-the-art treatment-planning and quality assurance procedures. Emphasis is placed on normal tissue sparing and delivery accuracy via the use of devices that ensure stability and beam location reproducibility. A rectal balloon with air filling will be used for prostate target immobilization and anatomical reproducibility, while a urethral catheter loaded with beacon transponders will be used to ensure set-up reproducibility and online target tracking. Previously untreated patients with low- or intermediate-risk prostate cancer will receive 24 Gy in a single-dose. Patients will be followed at one month post-treatment and every 3 months for up to 12 months (+/- 4 weeks) and every 6 months thereafter. Acute and chronic toxicity evaluations will focus, though not exclusively, on urinary, rectal and sexual functions and will be assessed through validated EPIC questionnaires. Serum PSA values will be drawn on the same schedule as clinical follow-up. A multi-parametric MRI will be performed at baseline, and at 6, 12 and 24 months following intervention. The study will be continuously monitored for a minimum of 5 years.

Official title: Phase II Study of Single-Dose Image-Guided Radiotherapy (SDRT) With Urethral Sparing for Localized Prostate Cancer

Key Details

Gender

MALE

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

200

Start Date

2019-06-01

Completion Date

2026-06

Last Updated

2019-07-29

Healthy Volunteers

No

Conditions

Interventions

RADIATION

IGRT 24 Gy Single dose

Previously untreated patients with prostate cancer will be treated with 24Gy in in one session.

PROCEDURE

Image-guided, volumetric intensity-modulated arc radiotherapy (IGRT-VMAT)

Patients enrolled in the study will undergo IGRT-VMAT with state-of-the-art treatment-planning and quality assurance procedures with emphasis on normal tissue sparing and delivery accuracy via the use of devices that ensure stability and beam location reproducibility.

DEVICE

Rectal balloon with air filling

A rectal balloon with air filling will be used for prostate target immobilization and anatomical reproducibility.

DEVICE

Urethral catheter loaded with beacon transponders

A urethral catheter loaded with beacon transponders will be used to ensure set-up reproducibility and online target tracking.

Locations (1)

Champalimaud Foundation

Lisbon, Portugal