NCT06462963Recruiting
OligoCare TwiCs (Trials Within Cohorts) Trial Comparing Acute Toxicity in Single-fraction vs Multiple-fraction SBRT for Metastasis-directed Treatment (SPRINT)
Summary
The goal of this clinical trial is to evaluate single-fraction metastases-directed SBRT in the broader radiation oncology community and to compare its safety and efficacy profile with the current Standard of Care (SoC) of multiple-fraction SBRT in patients with oligometastatic disease of primary breast, prostate, NSCLC and colorectal cancer having all lesions that will be treated with radical radiotherapy amenable to single-fraction SBRT. The main question/hypothesis this clinical trial aims to answer is: \- Single-fraction SBRT has comparable outcomes as those obtained with multiple fraction SBRT, both in terms of safety and efficacy. Patients from the OligoCare cohort will be randomized to receive either single-fraction SBRT or the current SoC of multiple-fraction SBRT.
Inclusion criteria
• Patient is part of the RP1822-OligoCare. As in OligoCare, ALL active cancer lesions (loco-regional primary and all oligometastases) were or will be treated with radical intent (surgery or radiotherapy). • All lesions that will be treated with radical radiotherapy have to be amenable to single-fraction SBRT. Concurrent systemic treatment is allowed. • Written informed consent must be given according to ICH/GCP, and national/local regulations. Patients will be consented in a step-wise approach. Step 1 \[both control and experimental arms\]: patients will need to consent to be included and evaluated in E²-RADIatE (that includes the non-interventional OligoCare prospective registry cohort) and to potentially be randomized to future sub-studies for which they are eligible; no further consent will be sought if they are randomized to the SoC (control) arm; Step 2 \[experimental arm only\]: if eligible for the current sub-study and randomized to receive single-fraction SBRT, patients will need to consent to receiving the experimental treatment.
Exclusion criteria
All targeted lesion judged by the treating physician to be associated with risks for severe toxicity following single-fraction SBRT. The following lesions are systematically excluded: • Pulmonary metastases within 1 cm of proximal bronchial tree, esophagus or brachial plexus • Metastases within \< 5 mm of any hollow GI structure: esophagus, stomach, small bowel, large bowel • Metastases within \< 5 mm of the spinal cord, the cauda equina or the brachial plexus • Metastases \> 5 cm in largest diameter.
Contacts
The trial team's contact details are shown on request.
See the official trial record- Status
- Recruiting
- Phase
- No phase (N/A)
- Study type
- Interventional
- Countries
- Switzerland, Italy, Belgium, Netherlands
- Sponsor
- European Organisation for Research and Treatment of Cancer - EORTC(Network / cooperative)
- Protocol no.
- EORTC-2387
- Conditions
- Breast Cancer, Prostate Cancer, NSCLC, Colorectal Cancer, Oligometastatic Disease
- Interventions
- Radiation
Treatments studied
- single-fraction SBRT
- multiple-fraction SBRT
Locations · 2
- Bern, SwitzerlandInselspital - InselspitalRecruiting at this site
- Zurich, SwitzerlandUniversitaetsSpital ZurichRecruiting at this site
In total, worldwide, 2 of the 15 sites listed in the registry are recruiting; the other 13 are not currently recruiting.
Site status per the ClinicalTrials.gov registry (last update posted: August 1, 2025).
This status may have changed and says nothing about your eligibility: before taking any step, check with your oncologist or the site.
See also
Other versions
These results are indicative and do not replace medical advice — discuss them with your doctor.