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Cryoablation of Low Risk Small Breast Cancer- Ice3 Trial

Primary Purpose

Breast Cancer

Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Ice-Sense3TM/ ProSenseTM
Sponsored by
IceCure Medical Ltd.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Breast Cancer focused on measuring cryoablation, cryotherapy, breast cancer

Eligibility Criteria

50 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  1. Competent to sign informed consent
  2. Diagnosis of invasive ductal breast carcinoma by core needle biopsy, meeting the following criteria:

    1. 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.
    2. 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.
    3. Nottingham grade 1-2. Specifically, nuclear and mitotic scores must be less than or equal to 2.
    4. Estrogen receptor positive, progesterone receptor positive, HER2 negative
  3. Age>= 50
  4. Breast size adequate for safe cryoablation
  5. Lesion must be sonographically visible at the time of treatment.
  6. 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:

  1. Presence of lobular carcinoma
  2. Presence of luminal B pathology
  3. Nottingham score of 3 (specially nuclear and mitotic score>2)

3. Presence of microinvasion, or invasive breast carcinoma with extensive intraductal component (EIC) 4. Presence of multifocal and/or multicentric in breast cancer 5. Presence of multifocal calcifications 6. Presence of prior or concurrent neoadjuvant chemotherapy for breast cancer

Sites / Locations

  • Ironwood Cancer & Research Centers
  • BreastLink
  • Bridgeport Hospital, Yale Medical School
  • Dalton Surgical Group
  • Indiana University
  • Karmanos Cancer Institute
  • Regional Medical Imaging
  • Comprehensive Breast Care
  • CentraState Medical Center
  • Breast Specialty care/ Presbyterian Hospital
  • Mount Sinai Beth Israel
  • Columbia University/ NY Presbyterian hospital
  • Weill Cornell Medical College
  • Montefiore Medical Center
  • Cincinnati Breast Surgeons Inc.
  • University hospitals cleveland medical center
  • Thomas Jefferson University hospital
  • West Clinic
  • Complete Breast Care

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

single arm, open label

Arm Description

Early stage Breast cancers up to 1.5cm

Outcomes

Primary Outcome Measures

local Inbreast Breast Tumor Recurrence (IBTR) rate
6 months post cryoabltion , then annually for 5 years

Secondary Outcome Measures

Complete ablation of primary tumor up to 60 months after cryoablation
Complete ablation of primary tumor
Improvement or maintenance of subject's quality of life
Quality of life will be assesed using NCCN DISTRESS THERMOMETER
Breast cosmetics satisfaction
subjects and physician satisfaction from the cosmetic results
Regional recurrence rate
Regional Invasive breast tumor recurrence rate.
Distant metastases rate
Distant metastases rate including contralateral Breast cancer
Disease-free Survival (DFS)
DFS from 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, second primary cancer, DCIS or invasive contralateral breast cancer, or death due to any cause
Overall survival
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.
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.
Adverse events
Adverse events related to study device or procedure rate

Full Information

First Posted
July 22, 2014
Last Updated
February 14, 2023
Sponsor
IceCure Medical Ltd.
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1. Study Identification

Unique Protocol Identification Number
NCT02200705
Brief Title
Cryoablation of Low Risk Small Breast Cancer- Ice3 Trial
Official Title
Cryoablation of Low Risk Breast Cancer Less Than 1.5 cm: An Evaluation of Local Recurrence (Ice3 Trial)
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
October 2014 (Actual)
Primary Completion Date
August 2024 (Anticipated)
Study Completion Date
December 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
IceCure Medical Ltd.

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
To evaluate the efficacy of cryoablation without lumpectomy and its impact on local and distant recurrence of early stage breast cancer .

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer
Keywords
cryoablation, cryotherapy, breast cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
208 (Actual)

8. Arms, Groups, and Interventions

Arm Title
single arm, open label
Arm Type
Other
Arm Description
Early stage Breast cancers up to 1.5cm
Intervention Type
Device
Intervention Name(s)
Ice-Sense3TM/ ProSenseTM
Primary Outcome Measure Information:
Title
local Inbreast Breast Tumor Recurrence (IBTR) rate
Description
6 months post cryoabltion , then annually for 5 years
Time Frame
up to 5 years
Secondary Outcome Measure Information:
Title
Complete ablation of primary tumor up to 60 months after cryoablation
Description
Complete ablation of primary tumor
Time Frame
up to 5 years from procedure date.
Title
Improvement or maintenance of subject's quality of life
Description
Quality of life will be assesed using NCCN DISTRESS THERMOMETER
Time Frame
at 6 months compare to the base line
Title
Breast cosmetics satisfaction
Description
subjects and physician satisfaction from the cosmetic results
Time Frame
up to 5 years from procedure data.
Title
Regional recurrence rate
Description
Regional Invasive breast tumor recurrence rate.
Time Frame
up to 5 years
Title
Distant metastases rate
Description
Distant metastases rate including contralateral Breast cancer
Time Frame
up to 5 years
Title
Disease-free Survival (DFS)
Description
DFS from 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, second primary cancer, DCIS or invasive contralateral breast cancer, or death due to any cause
Time Frame
up to 5 years
Title
Overall survival
Description
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
Time Frame
up to 5 years
Title
Breast Cancer Survival.
Description
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.
Time Frame
up to 5 years
Title
Adverse events
Description
Adverse events related to study device or procedure rate
Time Frame
up to 2 years for AEs and up to 5 years for SAEs

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Facility Information:
Facility Name
Ironwood Cancer & Research Centers
City
Glendale
State/Province
Arizona
ZIP/Postal Code
85306
Country
United States
Facility Name
BreastLink
City
Santa Ana
State/Province
California
ZIP/Postal Code
92705
Country
United States
Facility Name
Bridgeport Hospital, Yale Medical School
City
Trumbull
State/Province
Connecticut
ZIP/Postal Code
06611
Country
United States
Facility Name
Dalton Surgical Group
City
Dalton
State/Province
Georgia
ZIP/Postal Code
30720
Country
United States
Facility Name
Indiana University
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46202-5116
Country
United States
Facility Name
Karmanos Cancer Institute
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48201
Country
United States
Facility Name
Regional Medical Imaging
City
Flint
State/Province
Michigan
ZIP/Postal Code
48507
Country
United States
Facility Name
Comprehensive Breast Care
City
Troy
State/Province
Michigan
ZIP/Postal Code
48085
Country
United States
Facility Name
CentraState Medical Center
City
Freehold
State/Province
New Jersey
ZIP/Postal Code
07728
Country
United States
Facility Name
Breast Specialty care/ Presbyterian Hospital
City
Albuquerque
State/Province
New Mexico
ZIP/Postal Code
87114
Country
United States
Facility Name
Mount Sinai Beth Israel
City
New York
State/Province
New York
ZIP/Postal Code
10011
Country
United States
Facility Name
Columbia University/ NY Presbyterian hospital
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States
Facility Name
Weill Cornell Medical College
City
New York
State/Province
New York
ZIP/Postal Code
10065
Country
United States
Facility Name
Montefiore Medical Center
City
New York
State/Province
New York
ZIP/Postal Code
10467
Country
United States
Facility Name
Cincinnati Breast Surgeons Inc.
City
Cincinnati
State/Province
Ohio
ZIP/Postal Code
45227
Country
United States
Facility Name
University hospitals cleveland medical center
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44106
Country
United States
Facility Name
Thomas Jefferson University hospital
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19107
Country
United States
Facility Name
West Clinic
City
Germantown
State/Province
Tennessee
ZIP/Postal Code
38138
Country
United States
Facility Name
Complete Breast Care
City
Plano
State/Province
Texas
ZIP/Postal Code
75075
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Cryoablation of Low Risk Small Breast Cancer- Ice3 Trial

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