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CRYO-TOUCH: Cryoablation of the Primary Breast Tumor in Metastatic Breast Cancer

Civil Hospices of Lyon logo

Civil Hospices of Lyon

Status

Begins enrollment this month

Conditions

Metastatic Breast Cancer

Treatments

Procedure: Cryoablation
Other: Patient-Reported Outcome Assessment

Study type

Interventional

Funder types

Other

Identifiers

NCT07676344
69HCL25_0566

Details and patient eligibility

About

Metastatic breast cancer remains an incurable disease for most patients. While surgical treatment of the primary breast tumor is commonly performed in localized breast cancer, its role in metastatic breast cancer remains controversial due to the lack of demonstrated survival benefit and the potential interruption of systemic anticancer therapies.

Cryoablation is a minimally invasive outpatient procedure that destroys tumor tissue through controlled freezing. In localized breast cancer, cryoablation has shown promising results regarding local tumor control, safety, and patient quality of life. However, evidence regarding its use in metastatic breast cancer remains limited.The primary objective of this prospective single-center cohort study is to evaluate local tumor control 12 months after cryoablation of the primary breast tumor in patients with metastatic breast cancer.

Full description

Metastatic breast cancer remains an incurable disease for most patients. While surgical treatment of the primary breast tumor is commonly performed in localized breast cancer, its role in metastatic breast cancer remains controversial due to the lack of demonstrated survival benefit and the potential interruption of systemic anticancer therapies.

Cryoablation is a minimally invasive outpatient procedure that destroys tumor tissue through controlled freezing. In localized breast cancer, cryoablation has shown promising results regarding local tumor control, safety, and patient quality of life. However, evidence regarding its use in metastatic breast cancer remains limited.

Preliminary retrospective data and local clinical experience suggest that cryoablation of the primary breast tumor may be feasible, safe, and associated with favorable local control in selected patients with metastatic breast cancer. Additional prospective data are needed to better characterize its clinical outcomes and its potential role as an alternative local treatment option.

The primary objective of this prospective single-center cohort study is to evaluate local tumor control 12 months after cryoablation of the primary breast tumor in patients with metastatic breast cancer.

Secondary objectives include evaluation of procedure-related safety, postoperative complications, pain, quality of life, treatment interruption, and implementation outcomes such as acceptability, appropriateness, feasibility, fidelity, and sustainability among both patients and healthcare professionals.

The study hypothesizes that cryoablation of the primary breast tumor is associated with satisfactory local tumor control, acceptable safety, favorable quality of life outcomes, and high acceptability among patients and healthcare professionals.

Enrollment

42 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

42 participants in 1 patient group

Cryoablation
Other group
Description:
Participants with metastatic breast cancer and an eligible primary breast tumor undergoing cryoablation as part of their clinical management. Participants will undergo cryoablation of the primary breast tumor and will be followed for 12 months. Study-specific procedures include baseline and 12-month breast MRI assessments, pain evaluations, quality-of-life questionnaires, safety assessments, and implementation questionnaires.
Treatment:
Other: Patient-Reported Outcome Assessment
Procedure: Cryoablation

Trial contacts and locations

1

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Central trial contact

Julien PERON, MD; Thibaut REVERDY

Data sourced from clinicaltrials.gov

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