Freezing breast tumors: a new hope for metastatic cancer control?
NCT ID NCT07676344
First seen Jun 30, 2026 · Last updated Jul 01, 2026 · Updated 1 time
Summary
This study investigates cryoablation, a procedure that freezes and destroys tumor tissue, for treating the primary breast tumor in women with metastatic breast cancer. The goal is to see if this minimally invasive approach can control the local tumor for 12 months while patients continue their standard systemic therapy. The trial will also assess pain, quality of life, and safety. It includes 42 women whose metastatic disease is stable or responding to treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- cryoablation (freezing procedure)
- What this could lead to
- If successful, cryoablation could offer a minimally invasive option to control the primary breast tumor in metastatic breast cancer, potentially improving local symptoms and quality of life without interrupting systemic treatments.
- What could go wrong
- This is a small, early-phase study with only 42 participants, so results may not apply broadly. Cryoablation may not prevent tumor regrowth, and risks include infection, pain, or damage to nearby tissue.
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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About 42 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2026
An estimate. Start dates often move.
- Expected to finish
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Jan 2030
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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Female participants only
- 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: * Female aged ≥18 years. * Histologically confirmed metastatic breast carcinoma, regardless of histological subtype, hormone receptor status, HER2 status, or tumor grade. * Receiving systemic anticancer treatment for metastatic breast cancer, including chemotherapy, immunotherapy, endocrine therapy, targeted therapy, or combination regimens. * Clinical response or stable disease according to RECIST v1.1 on the most recent imaging assessment performed within 3 months before enrollment, except for the primary breast lesion, which may be progressing. * Eligible for cryoablation of the primary breast tumor: * ECOG Performance Status ≤2. * Effective contraception for women of childbearing potential. * Able and willing to provide written informed consent. Exclusion Criteria: * Contraindication to cryoablation according to the investigator and/or interventional radiologist. * Contraindication to gadolinium-enhanced breast MRI according to institutional practice and radiologist assessment. * Pregnant or breastfeeding women. * Participation in another interventional clinical study with an ongoing exclusion period or that could interfere with the present study according to investigator judgment. * Psychiatric disorder or any medical condition that, in the opinion of the investigator, could compromise study participation or compliance with study procedures. * Adults under legal protection or unable to provide informed consent. * Persons deprived of liberty by judicial or administrative decision. * Absence of health insurance coverage.
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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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Centre Hospitalier Lyon-Sud
Lyon, 69 495, France
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