STAR-TRAP

STAR-TRAP: Phase II clinical trial of using stereotactic body radiotherapy (SBRT) on first line androgen receptor targeted therapy for metastatic prostate cancer

Trial Summary:

The STAR-TRAP trial is a Phase II multicentre randomised controlled study investigating whether stereotactic body radiotherapy (SBRT) improves outcomes when added to first-line androgen receptor pathway inhibitors for patients with metastatic hormone-sensitive prostate cancer (mHSPC). Sponsored by the Institute of Cancer Research (ICR) and funded by Prostate Cancer UK, the trial includes two cohorts: the induced oligometastatic (iOM) group, consisting of patients whose poly-metastatic disease has been downstaged by systemic therapy, and the oligoprogressive (OP) group, comprising patients with limited disease progression on first-line therapy. The study evaluates whether consolidative SBRT alongside standard systemic treatment can enhance failure-free survival in the iOM cohort and delay treatment discontinuation in the OP cohort, while also assessing effects on overall survival, radiological progression-free survival, time to second progression, symptomatic skeletal events, and patient-reported outcomes. Imaging sub-studies using PSMA PET-CT and WBMRI aim to identify patients most likely to benefit. Patients will receive either systemic therapy alone or with SBRT to metastatic sites, following strict quality assurance protocols. Follow-up aligns with standard care to monitor treatment response, disease progression, and adverse effects. This trial could refine metastatic prostate cancer treatment, potentially establishing SBRT as a standard adjunct to systemic therapy.

Prostate SABR QA Summary:

All QA activity will be streamlined with previous trial QA, where applicable. Please contact the RTTQA Group directly using the contact details below to discuss.

QA ProcessQA ActivityRequired for TrialAdditional Details
Pre-AccrualFacility Questionnaire
Outlining Benchmark Case1 Case by all trial centres
Planning Benchmark Case1 prostate SBRT case, subject to streamlining.
New benchmark only if centre has changed technique/equipment since (please discuss process with RTTQA contact)
Dummy Run
During AccrualIndividual Case ReviewThe outlining and planning for at least the first cohort of patients recruited by each trial centre will be subject to review
Data collection
Dosimetry AuditSubject to streamlining via audit from clinical trial QA groups and UK dosimetry audit network groups
QA StreamliningPACE-A/B/C, PACE-NODES, PEARLS, PIVOTALboost
Oligomet SABR QA Summary:

All QA activity will be streamlined with previous trial QA or SABR QA programmes, where applicable. Please contact the RTTQA Group directly using the contact details below to discuss.

QA ProcessQA ActivityRequired for TrialAdditional Details
Pre-AccrualFacility Questionnaire2024 SABR QA Programme: FQ required
Outlining Benchmark CaseAll centres should already have ≥2 clinicians approved through streamlining or cascade training. Benchmark only if centre has <2 clinicians accredited (1 case per anatomical site)
Planning Benchmark CaseAll centres should already be credentialed through streamlining. Benchmark only if centre has changed technique/equipment since (please discuss process with RTTQA contact)
Dummy Run
During AccrualIndividual Case ReviewProspective: At least the 1st Patient for each metastatic site
Data collection
Dosimetry Audit
QA StreamliningCtE, SEP, HALT, TRAP, SARON, STAR-TRAP, ATLANTA, SOPRANO

RTTQA Contact: enh-tr.star-trapqa@nhs.net

Chief Investigator: Dr Julia Murray

Sponsor: Institute of Cancer Research (startrap-icrctsu@icr.ac.uk)

Funder: Prostate Cancer UK

CTU Contact: ICR Clinical Trials and Statistics Unit (ICR-CTSU) (startrap-icrctsu@icr.ac.uk)