INSPIRE: INnovative SABR for Prostate Cancer All IREland

Recruiting now · Phase 2

Conditions studied: Prostate Adenocarcinoma

In brief

This is a Phase II, single arm, multi-centre, prospective clinical trial evaluating next generation Stereotactic Ablative Radiotherapy (SABR) for low, intermediate, and eligible high-risk prostate cancer. Eligible patients will receive next generation prostate SABR incorporating toxicity reduction strategies

Key facts

Study ID

NCT07552168

Run by

Cancer Trials Ireland

People needed

136

Starts

2026-04-23

Expected to finish

2034-11-01

Last updated by the study team

2026-07-06

Who can join

Age: 18 and older. Sex: male. Healthy volunteers: not accepted.

You may qualify if…

• Written informed consent obtained prior to any study-related procedures
• Males ≥ 18 years of age
• ECOG performance status (PS) 0-2
• Biopsy-proven prostate adenocarcinoma without neuro-endocrine differentiation (within 18 months prior to registration, unless on active surveillance and re-biopsy not clinically indicated)
• Gleason score ≤ 4+3
• Clinical and/or MRI stage T1c-T3a, N0-X, M0-X
• PSA ≤ 30 ng/ml (within 60 days prior to registration / prior to starting androgen-deprivation therapy (ADT/hormone therapy) [PSA ≤ 15 ng/ml for patients on 5-alpha reductase inhibitors]
• Patients belonging to one of the following risk groups:
• Low risk - patients meeting all of the following criteria:
• Gleason ≤ 6
• Clinical stage T1c-T2a
• PSA < 10 ng/ml (within 60 days prior to registration)
• Intermediate risk - patients meeting any of the following criteria, assuming no high-risk features apply:
• Gleason 7 (3+4 or 4+3)
• MRI stage T2b-T2c (N0, M0-X)
• PSA 10-20 ng/ml (within 60 days prior to registration)
• High risk - patients with tumours that meet a maximum of one of the following criteria:
• MRI stage T3a (N0, M0)
• PSA >20 - ≤30 ng/ml (within 60 days prior to registration)

You may not qualify if…

• Previous malignancy within the last 2 years (except basal cell carcinoma (BCC) or squamous carcinoma of the skin), or if previous malignancy is expected to significantly compromise 5 year survival
• Prior pelvic radiotherapy
• Any prior active treatment for prostate cancer (with the exception of ADT). Patients previously on active surveillance are eligible if they continue to meet all other eligibility criteria.
• Life expectancy <5 years.
• Bilateral hip prostheses or any other implants/hardware that would introduce substantial CT artefacts
• Medical conditions likely to make radiotherapy inadvisable e.g. inflammatory bowel disease, significant urinary symptoms.
• Anticoagulation with warfarin/bleeding tendency making fiducial placement or surgery unsafe in the opinion of the clinician. Note: Anti-platelet agents e.g. aspirin, clopidogrel and DOACs such as apixaban, rivaroxaban are not contraindications to trial entry.
• Participation in another concurrent treatment protocol for prostate cancer (not including QoL, survivorship, exercise or registry studies).

Where it is running

• Bon Secours - UPMC Hillman — Cork, Ireland (enrolling)
• UPMC Hillman Cancer Centre at Whitfield Hospital — Waterford, Ireland (enrolling)
• St Luke's Centre for Radiation Oncology at Beaumont Hospital — Dublin, Leinster, Ireland
• Northern Ireland Cancer Centre (NICC) — Belfast, Ulster, United Kingdom

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.