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NCT Number: NCT06300125

Percutaneous Cryoablation of Low-risk Early Breast Cancer

Expand the current evidence base regarding percutaneous cryoablation of early-stage, low-risk breast tumors, integrated into the standard therapeutic pathway with well-defined follow-up data, as well as data on quality of life. Demonstrate, therefore, that the use of percutaneous cryoablation in the treatment of low-risk breast carcinoma is not inferior to surgery when combined with adjuvant radiotherapy and chemotherapy (when necessary). The hypothesis is that cryoablation, being simple and oncologically effective, ensures a better quality of life for the patient (reduced morbidity, no need for general anesthesia, improved cosmetic outcomes) and consequently has a lesser psychological impact, as well as a better cost-benefit ratio compared to the standard surgical approach.

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Key information

Age range

50 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

European Institute of Oncology

Milan, Italy

Location status: Recruiting

Location contact

Franco Orsi

CONTACT

About this study

PRECICE is a prospective single arm, single centre, observational study which aims to enroll patients ≥50 years old, diagnosed with early-stage luminal A/B, unifocal Breast Cancer (BC), < 15 mm in size, without in situ component detected at imaging (by breast ultrasound, Magnetic Resonance Imaging (MRI), Mammography) and confirmed by needle biopsy, defining histotype and biology. All patients that receive treatment with cryoablation as their standard care for BC followed by RadioTherapy (RT), according to the MultiDisciplinary Tumor Board (MDTB) referral and fulfil the inclusion criteria, will be prospectively included in the study.

Follow-up protocol involved breast imaging with mammography, ultrasound, and MRI, assessment of procedure failure rate, quality of life, psychological impact, oncological outcome and economical efficacy. Adjuvant therapy will be planned after further multidisciplinary discussion

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Tumour, Node, Metastasis stage (TNM) = dimension up to 15 mm as measured by breast ultrasound, MRI, Mammography, Node negative, absence of distant metastasis
  • Unifocality
  • All invasive cancer, except lobular
  • Biology= luminal A and luminal B* (Estrogen Receptor (ER) positive/human epidermal growth factor receptor-2 (HER2)negative) (Documented estrogen receptor (ER)-positive tumor assessed locally and defined as ≥10% of tumor cells stained positive.

Documented HER2-negative tumor (in accordance to 2018 American Society of Clinical Oncology guidelines, as determined per local assessment)

  • Any grade (G)
  • Radiological detection= breast ultrasound, MRI, Mammography
  • Tumor site= not located superficially (≥1 cm from the skin plane)
  • Breast size= any, appropriate for the procedure in relation to ultrasound examination
  • Referral to breast cryoablation by a multidisciplinary tumor board
  • Planned treatment with cryoablation using IceCure (TM-trade mark) system
  • Informed consent *Luminal B and G3 BC: previous specific patients' selection and Oncotype Dx [31] on cancer tissue from needle biopsy before procedure and eventual Prediction Analysis of Microarray 50 (PAM50) test.

Exclusion criteria

  • Plurifocality
  • Invasive lobular breast cancer
  • HER2 overexpressed or Triple Negative Breast Cancer (TNBC)
  • tumor dimension >15 mm
  • Node positive
  • post NeoAdjuvant ChemoTherapy (NACT) breast cancer
  • <50 years
  • Presence of intraductal component (DCIS)
  • Absence of psychological compliance in understanding and adhering to rationale of the study
  • Inability to perform MRI
  • Breast augmentation with implants

Treatment and study plan

Cryoablation

Procedure

Percutaneous Cryoablation of Breast Cancer

Primary outcomes

  1. Procedure failure rate

    Time frame: 8 months

    Percentage of patients with residual tumor at the site of cryoablation

Secondary outcomes

  1. Assessment of subject's quality of life in terms of evaluation of sources of distress

    Time frame: 60 months

    Quality of life will be assessed using National Comprehensive Cancer Network (NCCN) DISTRESS THERMOMETER

  2. Assessment of subject's satisfaction

    Time frame: 60 months

    Satisfaction will be assessed using BreastQ questionnaire

  3. Cost-analysis - evaluation of cost of intervention, hospitalization and re-intervention (if applicable)

    Time frame: 60 months

    Cost will be calculated for all patients considering the cost of the intervention, the cost of hospitalization and cost of eventual re-intervention in case of unsuccessful intervention

  4. Ipsilateral breast tumor recurrence

    Time frame: 60 months

    Percentage of ipsilateral breast tumor recurrence

  5. Distant metastasis

    Time frame: 60 months

    Percentage of distant metastasis

Study contacts

Contact information is provided by the study sponsor or research team.

Mara Negri

CONTACT

[email protected]

0039 02 57489536

Paolo Della Vigna, MD

CONTACT

[email protected]

0039 02 57489060

Sponsors and collaborators

Lead sponsor

European Institute of Oncology

Other

Collaborators

  • Fondazione Umberto Veronesi
  • IceCure Medical Ltd.

Registry information

Acronym: PRECICE

Important dates

Study start
2024
Primary completion
2026
Study completion
2031
First posted
Mar 8, 2024
Registry last updated
Jan 6, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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