New combo treatment may slow colorectal cancer spread
NCT ID NCT05862051
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This trial is for people with colorectal cancer that has spread to a few spots in the body but cannot be fully removed by surgery alone. After 3-4 months of standard chemotherapy, participants either continue chemotherapy alone or also receive local ablative therapy—such as surgery, radiation, or heat/cold ablation—to target remaining tumors. The goal is to see if adding this local treatment helps delay the cancer from growing further.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Local ablative therapy (surgery, radiation, or heat/cold ablation)
- What this could lead to
- If successful, this approach could extend the time before colorectal cancer worsens, offering a new way to manage the disease.
- What could go wrong
- This is a very small early-phase trial with only 6 participants, so results may not apply broadly. The added procedures also carry risks like infection or side effects from radiation.
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.
- 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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6 people
The number who actually took part.
- Started
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Dec 2021
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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A research network
The lead sponsor is a research network or cooperative group.
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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Metastatic colorectal adenocarcinoma that is not amenable to potentially oncological curative surgery alone. * Primary tumour must be controlled if the primary is intact, with no evidence of progression at primary site prior to study entry * Imaging demonstrating ongoing treatment benefit (partial response or stable disease as per RECIST criteria) after 3-4 months of standard first-line systemic treatment. * At least one metastatic lesion detected on CT +/- FDG-PET scan prior to first line systemic treatment AND on screening FDG-PET and CT scans, meeting the following criteria: 1. max of 3 lesions per organ except for the liver and lung 2. max of 5 lesions in the lung 3. no limitation to the number of liver lesions provided they are all amenable to LAT 4. max of 3 involved organs including a lymph node station 5. only one lymph node station involvement is allowed 6. for patients with liver metastases, a quadruple phase contrast enhanced CT or MRI liver is required to fully stage the liver; this can be performed prior to or within 4 weeks of commencing first line systemic treatment 7. staging FDG-PET scan is encouraged and can be performed prior to or within 4 weeks of commencing first line systemic treatment * All lesions can be safely treated by LAT as determined by multidisciplinary team meeting. Exclusion Criteria: * Deficient mismatch repair (dMMR) or microsatellite instability-high (MSI-high) tumour * BRAFV600E mutated tumour * Concurrent or previous other malignancy within 2 years of study entry, except curatively treated basal or squamous cell skin cancer, prostate intraepithelial neoplasm, carcinoma in-situ of the cervix, Bowen's disease or prostate cancer with a Gleason score ≤6. * Presence of brain, peritoneal, omental or ovarian metastases * Malignant pleural effusion or ascites.
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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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Barwon Health
Geelong, Victoria, 3220, Australia
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Bendigo Hospital
Bendigo, Victoria, 3550, Australia
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Border Medical Oncology
Albury, New South Wales, 2640, Australia
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Eastern Health
Box Hill, Victoria, 3128, Australia
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Northeast Health Wangaratta
Wangaratta, Victoria, 3677, Australia
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Peter MaCallum Cancer Centre
Melbourne, Victoria, 3000, Australia
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St Vincent's Hospital Melbourne
Fitzroy, Victoria, 3065, Australia
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The Northern Hospital
Epping, Victoria, 3076, Australia
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Western Health
Saint Albans, Victoria, 3021, Australia
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