NCT04498767Recruiting
Stereotactic Body Radiotherapy in Patients With Rare Oligometastatic Cancers (OligoRARE)
Summary
This is a randomized open-label multicentre Phase III superiority study of the effect of adding SBRT to the standard of care treatment on overall survival in patients with rare oligometastatic cancers. Patients will be randomized in a 1:1 ratio between current standard of care treatment vs. standard of care treatment + SBRT to all sites of known metastatic disease. The primary objective of this trial is to assess if the addition of stereotactic body radiotherapy (SBRT) to standard of care treatment improves overall survival (OS) as compared to standard of care treatment alone in patients with rare oligometastatic cancers.
Inclusion criteria
• Histologically confirmed malignancy with metastatic disease detected on imaging. Biopsy of metastasis is preferred, but not required. • Controlled primary tumour, defined as: • at least 3 months since original tumour treated definitively, with no progression at primary site • Total number of oligometastases of 1-5 including: • Brain metastases amenable to radiosurgery or fractionated stereotactic radiotherapy patient who had neurosurgical resection before trial inclusion are allowed and resected brain metastases count to the total number of oligometastases • All sites of disease can be safely treated based on the judgement of an experienced radiation oncologist • ECOG score 0-2 • Life expectancy \> 6 months • Age 18 or older • Before patient randomization, written informed consent must be given according to ICH/GCP, and national/local regulations.
Exclusion criteria
• Primary cancer of prostate, breast, lung or colorectal • Serious medical comorbidities precluding radiotherapy: • These include interstitial lung disease in patients requiring thoracic radiation, Crohn's disease in patients where the GI tract will receive radiotherapy, or ulcerative colitis where the bowel will receive radiotherapy and connective tissue disorders such as lupus or scleroderma. • For patients with liver metastases, moderate/severe liver dysfunction (Child Pugh B or C) • Substantial overlap with a previously treated radiation volume. Prior radiotherapy in general is allowed, as long as the composite plan meets dose constraints herein. For patients treated previously with radiation, biological effective dose calculations should be used to equate previous doses to the tolerance doses listed in the RTQA Guidelines. All such cases should be discussed with one of the study coordinators • Brain metastases only, without extra-cerebral metastases • Malignant pleural effusion, malignant ascites, meningeal carcinomatosis and peritoneal carcinomatosis • Maximum size of 6 cm for lesions outside the brain, except: • Bone metastases over 5 cm may be included, if in the opinion of the local radiation oncologist it can be treated safely (e.g. rib, scapula, pelvis) • Clinical or radiologic evidence of symptomatic spinal cord compression. Patients can be eligible if surgical resection has been performed, but the surgical site counts toward the total of up to 3 metastases. • Metastatic disease that invades any of the following: GI tract (including oesophagus, stomach, small or large bowel), mesenteric lymph nodes, or disseminated skin metastases and lymphangiosis • Pregnant or breast feeding women • Any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with the patient before randomization in the trial
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, France, Germany, Italy, Belgium, Poland, United Kingdom
- Sponsor
- European Organisation for Research and Treatment of Cancer - EORTC(Network / cooperative)
- Protocol no.
- EORTC 1945
- Conditions
- Gynecologic Cancer, Skin Cancer, Head and Neck Cancer, Sarcoma, Renal Cancer, Bladder Cancer, Upper Urinary Tract Carcinoma, Pancreatic Cancer, Hepatobiliary Cancer, Gastric Cancer, Small Bowel Cancer, Esophageal Cancer, Melanoma, Colon Cancer, Oligometastasis
- Interventions
- Radiation
Treatments studied
- Stereotactic body radiotherapy
- Palliative RT
Collaborators
Anticancer Fund, Belgium, Rising Tide Foundation
Locations · 13
- Bern, SwitzerlandInselspitalRecruiting at this site
- Zurich, SwitzerlandUniversitaetsSpital ZurichRecruiting at this site
- Lille, FranceCentre Oscar LambretRecruiting at this site
- Villejuif, FranceGustave RoussyRecruiting at this site
- Hamburg, GermanyUniversitaets Krankenhaus Eppendorf - Universitaetsklinikum Hamburg-Eppendorf KE - University Cancer CenterRecruiting at this site
- Milan, ItalyIstituto Europeo di OncologiaRecruiting at this site
- Anderlecht, BelgiumInstitut Jules BordetRecruiting at this site
- Ghent, BelgiumUniversitair Ziekenhuis GentRecruiting at this site
- Wilrijk, BelgiumGasthuiszusters Antwerpen - Sint-AugustinusRecruiting at this site
- Gdansk, PolandMedical University Of GdanskRecruiting at this site
- Warsaw, PolandMaria Sklodowska-Curie Memorial Cancer Centre - Maria Sklodowska-Curie National Research Institute of OncologyRecruiting at this site
- Birmingham, United KingdomUniversity Hospitals Birmingham NHS Foundation Trust (UHB) - UHB-Queen Elisabeth Medical CentreRecruiting at this site
- London, United KingdomRoyal Marsden Hospital - site: Chelsea, LondonRecruiting at this site
In total, worldwide, all 13 sites listed in the registry are recruiting.
Site status per the ClinicalTrials.gov registry (last update posted: August 26, 2024).
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.