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Evaluation of Changes in the Immunological Microenvironment Surrounding Subcutaneous Breast Cancer Metastases After Liquid Nitrogen Cryotherapy

Evaluation of Changes in the Immunological Microenvironment Surrounding Subcutaneous Breast Cancer Metastases After Liquid Nitrogen Cryotherapy: Descriptive Pilot Study.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05825547
Acronym
CRIMCAS
Enrollment
5
Registered
2023-04-24
Start date
2022-02-16
Completion date
2024-07-17
Last updated
2025-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

Keywords

cryotherapy, cytotoxicity

Brief summary

Cryotherapy is a cold ablation technique used in many tumor locations. The destruction of tissues by cryoablation preserves proteins and in particular anti-tumor antigens, which could induce the stimulation of an immune response. Compared to other interventional radiology techniques, cryotherapy induces a higher immunogenic response. Studies describe complex responses with elevated levels of activating NK cells, circulating and anti-tumor T cells, and pro-inflammatory and NF-KB dependent cytokines. In breast cancer, whether or not an immune response is triggered depends on the type of cryoablation used. Indeed, high intensity cryoablation (rapid freezing in one cycle of the entire tumor volume) seems to induce a tumor-specific immunodestructive response, whereas low frequency cryoablation (several small repetitive cycles until a sufficient volume of ice is obtained) does not induce an immunogenic response and can even induce an immunoregulation with immunotolerance of the tumor cells The University Hospital of Nîmes has recently acquired a new liquid nitrogen cryotherapy technique, more powerful than the one classically performed with Argon. This technique is used for palliative and analgesic purposes in patients with metastatic breast cancer presenting painful subcutaneous metastases. The aim of this study is to evaluate in these patients the changes in the tumor microenvironment and the immune response potentially induced by this very high intensity cryotherapy. The study investigators hypothesize that locoregional treatment with liquid nitrogen cryotherapy of subcutaneous breast cancer metastases will allow a systemic response through the induction of an immune response. A better understanding of the type of immune response induced will allow the development of combined therapeutic strategies with curative and not only palliative and analgesic aims.

Interventions

Cryotherapy treatment administered by an interventional radiologist: the cryotherapy needle is placed under local anesthesia, ultrasound monitoring in real time. A complete cryotherapy cycle is performed with: freezing until the entire tumor is frozen as judged by ultrasound, then thawing for the same duration and refreezing according to the same principle.

Sponsors

Centre Hospitalier Universitaire de Nīmes
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 95 Years
Healthy volunteers
No

Inclusion criteria

* The patient must have given their free and informed consent * The patient must be a member or beneficiary of a health insurance plan * Patient with metastatic breast cancer with painful subcutaneous metastases. * Patient eligible for cryotherapy. * Therapeutic decision of antalgic and palliative treatment by cryotherapy taken in Pluridisciplinary Consultation Meeting. * Patient available for 15-day follow-up.

Exclusion criteria

* The subject is in a period of exclusion determined by a previous study * The subject us unable to express their consent or refuses to sign the consent form * The patient is under safeguard of justice or state guardianship

Design outcomes

Primary

MeasureTime frameDescription
Description of the immunological makeup of the tumor before liquid nitrogen cryotherapy treatmentDay 0Cytometry by Time Of Flight (CyTOF®) mass cytometry analysis of biopsy samples to identify lymphocyte and macrophage populations and anti-tumor markers
Description of the immunological makeup of the tumor after liquid nitrogen cryotherapy treatmentDay 15Cytometry by Time Of Flight (CyTOF®) mass cytometry analysis of biopsy samples to identify lymphocyte and macrophage populations and anti-tumor markers

Secondary

MeasureTime frameDescription
Level of pain related to subcutaneous metastases after cryotherapy treatmentDay 0 immediately after cryotherapy treatment0-10 Visual analog scale. Higher scores mean worse outcome.
Pain related to subcutaneous metastases before cryotherapy treatmentDay 0 immediately before cryotherapy treatmentBrief Pain Inventory (BPI): score from 0-120. Higher scores mean worse outcome.
Patients' tolerance to cryotherapy treatmentDay 15Collection of complications and adverse events according to Common Terminology Criteria for Adverse Events (CTCAE) criteria
Patient reported quality of before cryotherapy treatmentDay 0European Organisation for Research and Treatment of Cancer - C30 (EORTC QLQ-C30). This questionnaire is composed of 30 items grouped into 15 scales. A good quality of life is associated with a high score for the functional scales and a low score for the symptom scales
Patient reported quality of after cryotherapy treatmentDay 15European Organisation for Research and Treatment of Cancer - C30 (EORTC QLQ-C30). This questionnaire is composed of 30 items grouped into 15 scales. A good quality of life is associated with a high score for the functional scales and a low score for the symptom scales
Pain related to subcutaneous metastases after cryotherapy treatmentDay 0 immediately after cryotherapy treatmentBrief Pain Inventory (BPI): score from 0-120. Higher scores mean worse outcome.
Level of pain related to subcutaneous metastases before cryotherapy treatmentDay 0 immediately before cryotherapy treatment0-10 Visual analog scale. Higher scores mean worse outcome.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026