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Not Yet RecruitingNCT04571762

Adaptive MR-guided SBRT for Localized Prostate Cancer

Feasibility Trial of Individualized Daily Dose Adaptation for Localized Prostate Cancer by Online MR-guided SBRT

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
12 (estimated)
Sponsor
University of Zurich · Academic / Other
Sex
Male
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate a technical feasibility of MR-guided SBRT fraction dose adaptation for low-risk, intermediate-risk and low-volume metastatic prostate cancer. .

Detailed description

Hypofractionated SBRT to 36.25 Gy in 5 fractions (fraction dose 7.25 Gy) for low- and intermediate risk prostate cancer is standard of care. Using higher fraction doses that might be beneficial for disease control is not safe in all patients, unless adaptive treatment is performed. In this clinical trial the feasibility of online MR-guided SBRT fraction dose adaptation (between 7 and 8 Gy) for prostate cancer will be investigated. A fraction dose to the planning target volume (PTV) will be adapted to organs-at-risk (OAR) geometry (position, shape and volume) on online planning MRI scans of the treatment day ("geometry-of-the-day"). Thus the investigators hope to maximize treatment individualization.

Conditions

Interventions

TypeNameDescription
RADIATIONStereotactic Body Radiation Therapy (SBRT)SBRT (a fraction dose adapted to the OAR geometry-of-the-day, 5 fractions) performed on the MR-Linac

Timeline

Start date
2024-09-30
Primary completion
2025-09-30
Completion
2026-05-30
First posted
2020-10-01
Last updated
2024-05-23

Source: ClinicalTrials.gov record NCT04571762. Inclusion in this directory is not an endorsement.

Adaptive MR-guided SBRT for Localized Prostate Cancer (NCT04571762) · Clinical Trials Directory