Can radiation start before a cancer biopsy? trial tests a faster path for patients in pain
NCT ID NCT06156800
First seen Oct 02, 2026 · Last updated Oct 02, 2026
Summary
Doctors usually wait for biopsy results before giving radiation, but that wait can be long and painful for patients with advanced cancer. This trial tests whether giving palliative radiation first, before a biopsy confirms cancer, is safe and practical for a carefully selected group of adults who need urgent symptom relief. Researchers will track how often the radiation turns out to have been inappropriate once biopsy results arrive, and whether biopsies taken from radiated areas still give accurate diagnoses.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- palliative radiation therapy delivered before a biopsy
- What this could lead to
- If it works, this approach could let patients with urgent cancer symptoms start radiation sooner instead of waiting weeks for biopsy results.
- What could go wrong
- This is a small, early-phase feasibility trial, so it cannot prove the approach is safe or effective. Some patients might receive radiation for a non-cancerous condition, or the biopsy might not yield a clear diagnosis.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 48 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2024
- Expected to finish
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Apr 2028
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.
Who is studied
Participants with convincing clinical/radiological evidence of cancer, ineligible for curative treatment and awaiting a biopsy.
- 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 years or older * Willing to provide informed consent * Palliative treatment intent: either metastatic or incurable locally advanced disease * Tissue diagnosis is not required for determination of dose/fractionation scheme * Recent cross-sectional imaging \[for example - Computed Tomography (CT), Magnetic Resonance Imaging (MRI), Positron Emission Tomography/Computed Tomography (PET/CT)\] of the area to be treated, done within the past 3 months * Treating physician considers the pre-test probability of cancer greater than 95 percent based on clinical judgement and radiological findings. * The patient has at least 1 site of cancer amenable to biopsy * As per standard practices, if the radiation oncologist will be radiating the only site available to biopsy, they should proceed with caution. Participants should only be enrolled on trial if the risk of harm from delaying Radiation Therapy (RT) significantly outweighs the risks of possible non-diagnostic tissue. If the participant may potentially be eligible for systemic therapy, the treating radiation oncologist should consult a medical oncologist for an opinion regarding the risks of non-diagnostic molecular testing. The weighing of these priorities should be thoroughly discussed with the participant and the discussion should be documented. * Reasons for radiating a participant with a single lesion prior to biopsy include: * Spinal cord compression (actual or impending) and inoperable * Brain metastasis with significant symptoms or neurologic deficits and inoperable * Other lesions causing neurologic deficit * Pulmonary lesion causing or threatening lung obstruction * Uncontrolled bleeding (including hemoptysis and hematuria) * Superior vena cava obstruction (actual or impending) * Limited upside to molecular testing, as determined by the medical oncologist (for example - participant unfit for available systemic therapies, limited options for systemic therapy) * Radiation is considered urgent (for example - participant should receive radiation prior to biopsy date) o Urgent indications may include but are not limited to the reasons listed previously, as well as the following: * Painful metastases or primary lesion not adequately responding to analgesia * Symptomatic brain metastases * Bleeding * Impending pathologic fracture Exclusion Criteria: * Participant is potentially eligible for curative treatment * Clinical suspicion of lymphoma o Some features may be suggestive of lymphoma, including fever or night sweats (for example - B symptoms excluding weight loss), or imaging showing well-defined, homogenous lymphadenopathy. These findings are not exclusion criteria specifically, but should be considered by the clinician in formulating their differential diagnosis.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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London Regional Cancer Program, London Health Sciences Centre
RECRUITINGLondon, Ontario, N6A 5W9, Canada
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