Stereotactic Body Radiotherapy in Addition to Standard of Care Treatment in Patients With Rare Oligometastatic Cancers (OligoRARE): a Randomized, Phase 3, Open-label Trial

Status: Recruiting
Location: See all (13) locations...
Intervention Type: Radiation
Study Type: Interventional
Study Phase: Not Applicable
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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.

Locations
Other Locations
Belgium
Institut Jules Bordet
RECRUITING
Anderlecht
Universitair Ziekenhuis Gent
RECRUITING
Ghent
Gasthuiszusters Antwerpen - Sint-Augustinus
RECRUITING
Wilrijk
France
Centre Oscar Lambret
RECRUITING
Lille
Gustave Roussy
RECRUITING
Villejuif
Germany
Universitaets Krankenhaus Eppendorf - Universitaetsklinikum Hamburg-Eppendorf KE - University Cancer Center
RECRUITING
Hamburg
Italy
Istituto Europeo di Oncologia
RECRUITING
Milan
Poland
Medical University Of Gdansk
RECRUITING
Gdansk
Maria Sklodowska-Curie Memorial Cancer Centre - Maria Sklodowska-Curie National Research Institute of Oncology
RECRUITING
Warsaw
Switzerland
Inselspital
RECRUITING
Bern
UniversitaetsSpital Zurich
RECRUITING
Zurich
United Kingdom
University Hospitals Birmingham NHS Foundation Trust (UHB) - UHB-Queen Elisabeth Medical Centre
RECRUITING
Birmingham
Royal Marsden Hospital - site: Chelsea, London
RECRUITING
London
Contact Information
Primary
EORTC HQ
eortc@eortc.org
+32 2 7744 1611
Time Frame
Start Date: 2021-06-10
Estimated Completion Date: 2030-02-01
Participants
Target number of participants: 200
Treatments
Active_comparator: Arm 1: Standard of Care + palliative RT
Radiotherapy for patients in the standard arm should follow the principles of palliative radiotherapy as per the individual institution, with the goal of alleviating symptoms or preventing imminent complications. Recommended dose fractionations in this arm will include 8 Gy in 1 fractions, 20 Gy in 5 fractions, and 30 Gy in 10 fractions. Patients in this arm should not receive stereotactic doses or radiotherapy boosts, unless there is a clearly known clinical benefit (e.g. stereotactic radiation to a new brain metastases when all disease is controlled on systemic therapy).~Systemic therapy will be pre-specified based on the standard of care approach for that patient, and it may include cytotoxic, targeted, hormonal, or immunotherapy.
Experimental: Arm 2: Standard of Care + SBRT
The experimental arm consists of SBRT (and standard of care systemic therapy). Each lesion may be treated with 1, 3, or 5 SBRT fractions of 16-24 Gy, 24-33 Gy or 25-40 Gy, respectively, depending on the local practice and size \& location of oligometastases. Three-fraction regimens will deliver a fraction every second day, and five-fraction regimens are delivered daily. All treatments must be completed within 2 weeks (10 working days) in order to avoid delays in starting systemic therapy.~Patients treated with prior or concomitant systemic therapy are eligible for this study. Use of chemotherapy regimens, targeted therapy or immunotherapy containing potent enhancers of radiation damage (e.g. gemcitabine, doxorubicin) can be postponed or interrupted for a duration of one month after radiation.
Sponsors
Leads: European Organisation for Research and Treatment of Cancer - EORTC
Collaborators: Rising Tide Foundation, Anticancer Fund, Belgium

This content was sourced from clinicaltrials.gov

Similar Clinical Trials