About this trial
The goal of this clinical trial is to evaluate the feasibility of single-blind randomization between two palliative regimens - standard 24 Gray in 3 fractions vs a high-dose (Hi-D) 27 Gray in 3 fractions with dose escalation within the tumor in participants with bulky metastatic cancer.
The main question
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age 18 or older.
Able to provide informed consent
Patient has histologically confirmed solid tumour malignancy
ECOG performance status 0 - 2
Disqualifiers
- Hematologic malignancy.
Disease limited to intracranial sites
Serious medical co-morbidities precluding radiotherapy
Bone metastases with no soft tissue component
Trial design
Parallel
Treatments tested in this trial
Palliative Radiotherapy
Radiationstandard dose RT
Palliative Radiotherapy
Radiationhigh-dose RT
Treatment groups
Trial outcomes
Primary outcomes
Feasibility of accrual
≥20 participants enrolled within 24 months from first patient accrued
Feasibility of blinding
Trial Assignment Questionnaire administered post-treatment.
Secondary outcomes
Compare changes in local control
Kaplan-Meier curves; stratified log-rank test
Compare changes in OS
Time from randomization to death from any cause. Kaplan-Meier; stratified log-rank.
Sponsors and contacts
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