Zap and delay: radiation may buy time for cancer patients
NCT ID NCT02756793
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether giving precise, high-dose radiation to a small number of growing cancer spots can help people with metastatic non-small cell lung cancer stay stable longer. About 90 adults whose cancer has started to grow in just a few places while on standard treatment will either continue their usual care or also receive radiation to those spots. The goal is to see if this approach delays the next overall cancer progression.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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90 people
The number who actually took part.
- Start date
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Oct 2016
- Expected to finish
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Jun 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Alberta Health Services-Cross Cancer Institute
Edmonton, Alberta, T6G 1Z2, Canada
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BC Cancer - Prince George
Prince George, British Columbia, V2M 7E9, Canada
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BC Cancer - Victoria Centre
Victoria, British Columbia, V8R 4X1, Canada
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BC Cancer Agency Branch
Vancouver, British Columbia, V5Z 4E6, Canada
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BC Cancer Fraser Valley Centre
Surrey, British Columbia, V3V 1Z2, Canada
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London Regional Cancer Program
London, Ontario, N6A 4L6, Canada
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Princess Margaret Cancer Centre
Toronto, Ontario, M5G1X6, Canada
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Other studies related to the condition(s) this trial covers.
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