MR-guided Tumour Boost With Stereotactic Body Radiotherapy in Prostate Cancer

Status: Recruiting
Location: See location...
Intervention Type: Radiation
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This is a single-arm feasibility study that is recruiting 40 patients with histologically-proven localized prostate cancer and MRI-defined lesion(s). Participants in this study will get MR-guided radiotherapy boost to MRI visible tumour before or after whole gland radiation. Participants will be followed-up as per standard of care schedule up to 5 years post-treatment.

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

• Histologically-proven localized prostate cancer.

• Low, Intermediate, and High-risk prostate cancer (ideally limited to 1 risk factor)

• Low-risk: cT1-T2a, PSA \<10, and Gleason score 6

• Intermediate-risk: cT2b-c, PSA 10-20, and/or Gleason score 7

• High-risk limited to 1 risk factor: \>T2, PSA \>20, or Gleason score \>7

• Intra-prostatic tumour(s) demonstrated on mpMRI histologically confirmed limited to =/\< 1/3 total prostate volume

• Planned for EBRT (+/- ADT)

• ECOG 0 or 1

• 18 years of age or older

• Ability to provide written informed consent to participate in the study

Locations
Other Locations
Canada
University Health Network, Princess Margaret Hospital
RECRUITING
Toronto
Contact Information
Primary
Peter Chung, MD
peter.chung@uhn.ca
416-946-4501
Time Frame
Start Date: 2023-02-06
Estimated Completion Date: 2030-06
Participants
Target number of participants: 40
Treatments
Experimental: MR-guided Tumour Boost with SBRT
MR-guided radiotherapy boost to MRI visible tumour
Related Therapeutic Areas
Sponsors
Leads: University Health Network, Toronto

This content was sourced from clinicaltrials.gov

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