European Institute of Oncology
Milan, Italy
Location status: Recruiting
Location contact
Franco Orsi
CONTACT
NCT Number: NCT06300125
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.
Interested in participating?
Request Info50 year and older
All sexes
Observational
Milan, Italy
Location status: Recruiting
Franco Orsi
CONTACT
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
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Documented HER2-negative tumor (in accordance to 2018 American Society of Clinical Oncology guidelines, as determined per local assessment)
Exclusion criteria
Percutaneous Cryoablation of Breast Cancer
Time frame: 8 months
Percentage of patients with residual tumor at the site of cryoablation
Time frame: 60 months
Quality of life will be assessed using National Comprehensive Cancer Network (NCCN) DISTRESS THERMOMETER
Time frame: 60 months
Satisfaction will be assessed using BreastQ questionnaire
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
Time frame: 60 months
Percentage of ipsilateral breast tumor recurrence
Time frame: 60 months
Percentage of distant metastasis
Contact information is provided by the study sponsor or research team.
Mara Negri
CONTACT
Paolo Della Vigna, MD
CONTACT
European Institute of Oncology
Other
Acronym: PRECICE
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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