Elective Adaptive Radiation With SBRT for Improved DurabilitY of Response

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexMale
Age18+
SponsorUniversity Health Network, Toronto

About this trial

This prospective, single-arm feasibility study will include patients with prostate cancer that have controlled local disease diagnosed with oligorecurrent para-aortic nodal disease and/or common iliac nodal disease detected by PSMA PET or conventional CT/MRI imaging, and these patients will undergo CT-guided online adaptive SBRT to the tumor and elective SBRT to adjacent at-risk nodal regions.

Eligibility criteria

Qualifiers

Histologically confirmed prostate adenocarcinoma.

Oligorecurrent para-aortic +/- common iliac nodal disease planned for SBRT.

≤10 involved para-aortic (defined as between L1/L2 interface and L4/L5 interface) +/- common iliac LN on PSMA PET imaging.

ECOG performance status 0-2.

Disqualifiers

Prior radiotherapy to the nodal echelon (PA +/- common iliac).

Active secondary malignancy, except for adequately treated non-melanoma skin cancer.

Presence of significant comorbidities or medical conditions that may compromise the ability to undergo radiotherapy or participate in the study.

Contraindication to radiation.

Trial design

Treatments tested in this trial

  • Adaptive radiotherapy using SBRT

Treatment groups

26 Participants
are divided into 1 treatment group