NCT Number: NCT02200705
Cryoablation of Low Risk Small Breast Cancer- ICE3 Trial
To evaluate the efficacy of cryoablation without lumpectomy and its impact on local and distant recurrence of early stage breast cancer .
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Notify MeKey information
Conditions
Age range
50 year and older
Sex eligibility
Female
Study type
Interventional
Phase
Not applicable
Primary location
Ironwood Cancer & Research Centers, Glendale, Arizona, United States
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Competent to sign informed consent
- Diagnosis of invasive ductal breast carcinoma by core needle biopsy, meeting the following criteria:
- Unifocal primary disease NOTE: Patients with multifocal and/or multicentric in breast cancer, or evidence of EIC are NOT eligible. Patients with contralateral disease will remain eligible.
- Tumor size ≤1.5 cm in greatest diameter in the axis parallel to the treatment probe AND ≤1.5 cm in the axis anti-parallel to the treatment probe AND ≤1.5 cm in Anterior/ Posterior dimension. Tumor size ≤1.5 cm in greatest diameter as measured by breast ultrasound, mammogram and/or MRI. The largest dimension measured will be used to determine eligibility.
- Nottingham grade 1-2. Specifically, nuclear and mitotic scores must be less than or equal to 2.
- Estrogen receptor-positive, progesterone receptor-positive, HER2 negative
- Age>= 50
- Breast size adequate for safe cryoablation
- Lesion must be sonographically visible at the time of treatment.
- History of previously treated ipsilateral or contralateral breast carcinoma is not an exclusion criteria if the investigator is certain newly diagnosed carcinoma is new unifocal primary tumor.
Exclusion criteria
- Presence of lobular carcinoma
- Presence of luminal B pathology
- Nottingham score of 3 (specially nuclear and mitotic score>2)
- Presence of microinvasion, or invasive breast carcinoma with extensive intraductal component (EIC)
- Presence of multifocal and/or multicentric in breast cancer
- Presence of multifocal calcifications
- Presence of prior or concurrent neoadjuvant chemotherapy for breast cancer
- Presence of prior en bloc open surgical biopsy and/or lumpectomy for diagnosis/treatment of the index breast cancer
- Patient that is not suitable to cryoablation procedure according to the physician opinion
- ER AND PR negative, or Her2 positive noted on pre-cryo biopsy
Treatment and study plan
Primary outcomes
-
Local Inbreast Breast Tumor Recurrence (IBTR) Rate
Time frame: up to 5 years
6 months post cryoabltion, then annually for 5 years
Secondary outcomes
-
Complete Primary Tumor Ablation Rate
Time frame: up to 5 years from procedure date.
Complete ablation of primary tumor up to 60 months after cryoablation, reported as the percentage of patients with complete tumor ablation.
-
Improvement or Maintenance of Subject's Quality of Life
Time frame: Baseline and 6 months
Quality of life will be assessed using the NCCN Distress Thermometer, a 0-10 scale measuring patient distress (0 = no distress, 10 = extreme distress; higher scores indicate worse distress), collected at baseline and at 6 months follow-up visit.
-
Breast Cosmetics Satisfaction
Time frame: Up to 5 years following procedure
Participants and treating physicians rated satisfaction with cosmetic outcomes following breast cryoablation.
-
Regional Recurrence Rate
Time frame: up to 5 years following procedure
Regional Invasive breast tumor recurrence rate.
-
Distant Metastases Survival Rate
Time frame: up to 5 years following procedure
Distant metastases survival rate, including contralateral Breast cancer
-
Disease-free Survival (DFS)
Time frame: up to 5 years
DFS from the date of complete ablation of the primary tumor until the first disease event, where the disease event is defined as local (DCIS or invasive), regional, or distant breast cancer recurrence, or DCIS or invasive contralateral breast cancer.
-
Overall Survival
Time frame: up to 5 years
Overall survival from the date of the cryoablation until the date of death from any cause or up to the 60 months follow up visit
-
Breast Cancer Survival.
Time frame: up to 5 years
Breast Cancer Survival from the date of cryoablation until the date of death from breast cancer or up to the 60 months follow-up visit.
Sponsors and collaborators
Lead sponsor
IceCure Medical Ltd.
Industry
Registry information
Official study title
Cryoablation of Low Risk Breast Cancer Less Than 1.5 cm: An Evaluation of Local Recurrence (Ice3 Trial)
Important dates
- Study start
- 2014
- Primary completion
- 2024
- Study completion
- 2024
- First posted
- Jul 25, 2014
- Registry last updated
- Jul 7, 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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