🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Contributor sign in
Latest
Clinical Trials in Canada / NCT02756793
Active, not recruiting Not applicable

Stereotactic Radiotherapy for Oligo-Progressive Metastatic Cancer (The STOP Trial)

NCT02756793 · tracked via the Priya Life Science Canada tracker
Phase
Not applicable
Started
2016-10
Last updated
2025-12-31

Condition(s) studied

Metastatic Cancer

Investigational drug(s) / intervention(s)

Stereotactic Ablative Radiotherapy (SABR)Standard of Care Treatment

Stereotactic Ablative Radiotherapy (SABR): Patients will receive stereotactic ablative radiotherapy to all sites of progressive disease, with continuation of current systemic agents.

Standard of Care Treatment: May include: * Continue with current systemic agent(s) * Observation * Switch to next-line treatment Palliative radiotherapy is allowed in this arm.

Study summary

A multicenter randomized phase II trial of stereotactic body radiotherapy for oligo-progressive metastatic cancers. Eligible patients will be randomized in a 1:2 ratio between receiving their standard of care therapy or stereotactic ablative radiotherapy (SABR) to all sites of oligo-progressive lesions.Radiotherapy will be administered as soon as possible following randomization, and subjects will be followed until next disease progression. The primary outcome is progression-free survival (PFS).

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age 18 or older * Willing to provide informed consent * Histologically confirmed Non-Small Cell Lung Cancer (NSCLC) with metastatic disease detected on imaging. Biopsy of metastasis at some time point prior to enrollment is preferred, but not required. * Eastern Cooperative Oncology Group (ECOG) performance status 0-2 * Life expectancy \> 3 months * Patient has received treatment with systemic therapy (either cytotoxic or targeted, including maintenance therapies) during the past 6 weeks. This most recent systemic therapy agent must have been delivered for a total of at least 3 months, with an initial partial response (PR), complete response (CR) or stable disease (CR) prior to the development of oligo-progressive lesions. * Oligoprogression, defined as Response Evaluation Criteria in Solid Tumors (RECIST)-documented progression in up to 5 individual lesions, with no previous radiation or radiofrequency ablation to those sites. Oligoprogression may be defined as: * Progression of an individual metastasis according to RECIST 1.1 criteria * Unambiguous development of a new metastatic lesion at least 5mm in size * Progressive enlargement of a known metastasis on 2 consecutive imaging studies 2- 3 months apart with a minimum 5mm increase in size from baseline * All sites of oligoprogression can be safely treated * Maximum 3 progressing metastases in any single organ system (i.e. lung, liver, brain, bone), and the total number of metastases must be 5 or less Note for Patients with Brain Metastases: For patients with brain metastases and oligo-progression elsewhere where stereotactic radiation to the brain is deemed to be warranted, this must be specified prior to randomization. If randomized to Standard Arm, patient would receive stereotactic radiation to brain only. If randomized to Experimental Arm, patient would receive stereotactic radiation to brain and to body lesions Exclusion Criteria: * Serious medical comorbidities precluding radiotherapy, such as ataxia-telangiectasia or scleroderma. For patients with oligoprogressive lesions in the lung or thorax, this includes interstitial lung disease * Prior radiotherapy to a site requiring treatment * Malignant pleural effusion * Inability to treat all sites of enlarging, oligoprogressive disease * Clinical or radiological evidence of spinal cord compression or tumor within 3mm of spinal cord on MRI * Any other condition which in the judgment of the investigator would make the patient inappropriate for entry into this study

Primary outcome measure(s)

Trial sites (7)

FacilityCityRegionStatus
Alberta Health Services-Cross Cancer Institute Edmonton Alberta
BC Cancer - Prince George Prince George British Columbia
BC Cancer Fraser Valley Centre Surrey British Columbia
BC Cancer Agency Branch Vancouver British Columbia
BC Cancer - Victoria Centre Victoria British Columbia
London Regional Cancer Program London Ontario
Princess Margaret Cancer Centre Toronto Ontario

More London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's trials in Canada

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT02756793 on ClinicalTrials.gov ↗ ← All trials in Canada