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Magnetic Marker Localization for Occult Breast Cancer and Target Axillary Dissection in Node-positive Breast Cancer Post-neoadjuvant Chemotherapy (MaCTAD)

Primary Purpose

Breast Neoplasm, Chemotherapy Effect

Status
Recruiting
Phase
Not Applicable
Locations
Hong Kong
Study Type
Interventional
Intervention
Magnetic seed localization
Sponsored by
The University of Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Breast Neoplasm

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • All patients with cT1-3N1 invasive ductal carcinoma planned for neoadjuvant chemotherapy and/or target therapy
  • mentally competent to give informed consent
  • Agreed to proceed with curative operation after chemotherapy and tentatively keen for breast conservative surgery and targeted axillary dissection after neoadjuvant chemotherapy
  • Radiologically 1-3 ipsilateral axillary lymph node metastases confirmed by cytology or biopsy

Exclusion Criteria:

  • Presence of distant metastasis, inflammatory breast cancers, multi-centric breast cancers
  • History of previous ipsilateral axillary surgery or irradiation
  • Hypersensitivity to dextran compounds or iron
  • Iron overload disease
  • Pregnant or lactating patients
  • Patients with pacemaker or other implantable metallic devices in chest wall or prosthesis in shoulder
  • Mentally incompetent patients

Sites / Locations

  • University of Hong KongRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Study arm

Arm Description

Magnetic seed guided lumpectomy and targeted axillary dissection

Outcomes

Primary Outcome Measures

Successful localization of breast tumor and axillary lymph node
Successful surgical retrieval of magnetic seed marked breast tumor and axillary lymph node in intraoperative specimen mammogram (in percentage)

Secondary Outcome Measures

Percentage of patients that can avoid axillary lymph node dissection
Percentage of patients that can achieve nodal pathological complete response after neoadjuvant chemotherapy
Percentage of successful magnetic seed guided lumpectomy
Percentage of involved or close margins in lumpectomy specimen which require re-excision
Level of satisfaction from surgeons and radiologists
Level of satisfaction from surgeons and radiologists which will be determined by the satisfaction questionnaire
5-year local regional recurrence rate
5-year ipsilateral breast tumor recurrence rate and/or axillary recurrence rate

Full Information

First Posted
May 16, 2022
Last Updated
June 16, 2022
Sponsor
The University of Hong Kong
Collaborators
Endomagnetics Ltd.
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1. Study Identification

Unique Protocol Identification Number
NCT05427071
Brief Title
Magnetic Marker Localization for Occult Breast Cancer and Target Axillary Dissection in Node-positive Breast Cancer Post-neoadjuvant Chemotherapy
Acronym
MaCTAD
Official Title
Magnetic Marker Localization for Occult Breast Cancer and Target Axillary Dissection in Node-positive Breast Cancer Post-neoadjuvant Chemotherapy
Study Type
Interventional

2. Study Status

Record Verification Date
June 2022
Overall Recruitment Status
Recruiting
Study Start Date
October 15, 2020 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2028 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The University of Hong Kong
Collaborators
Endomagnetics Ltd.

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The use of neoadjuvant chemotherapy in breast cancer is expanding in the recent decade. Patients with good response to neoadjuvant chemotherapy could benefit from de-escalation of breast and axilla operation. However, breast tumor and involved axillary lymph node should be marked before the commencement of chemotherapy. This could facilitate subsequent operative planning and intraoperative assessment of disease response. This study aims to evaluate the feasibility of magnetic marker localization for non-palpable breast cancer and targeted axillary dissection in patients with node-positive breast cancer following neoadjuvant therapy
Detailed Description
Eligible patients will receive ultrasound guided placement of magnetic seeds (Magseed®) within the cortex of the sampled lymph node and epicenter of the breast tumor by radiologists before commencement of neoadjuvant treatment. Chemotherapeutic regimes will be determined by oncologists in charge. During the period of neoadjuvant treatment, patients will be followed up by oncologists and surgeons with clinical assessment of tumor response according to our usual practice. After completion of neoadjuvant chemotherapy, recruited patients will receive mammography and ultrasonography assessment before surgery. Breast conservative surgery with targeted axillary dissection will be offered when feasible. In patients not suitable for breast conservative surgery, mastectomy and targeted axillary dissection with or without immediate breast reconstruction will be offered. Patient will receive localization of previously marked axillary lymph node and breast tumor and sentinel lymph node biopsy by magnetic means completely, i.e. by the use if magnetic seeds and superparamagnetic iron oxide injection. Radioisotope with Tc-99 is injected prior to operation as backup plan for sentinel lymph node biopsy. The clipped lymph node and sentinel lymph nodes are sent for frozen section analysis. If any of the lymph nodes is positive for malignancy, axillary dissection will be performed. Similarly, the breast tumor will be resected with guidance of magnetometer and specimen mammogram will confirm the presence of tumor and magnetic seeds.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Neoplasm, Chemotherapy Effect

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
All patients received magnetic seeds guided localization of axillary lymph node and breast tumor and superparamagnetic iron oxide-guided sentinel lymph node biopsy
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Study arm
Arm Type
Experimental
Arm Description
Magnetic seed guided lumpectomy and targeted axillary dissection
Intervention Type
Device
Intervention Name(s)
Magnetic seed localization
Intervention Description
Magnetic seed guided localization
Primary Outcome Measure Information:
Title
Successful localization of breast tumor and axillary lymph node
Description
Successful surgical retrieval of magnetic seed marked breast tumor and axillary lymph node in intraoperative specimen mammogram (in percentage)
Time Frame
At the time of operation
Secondary Outcome Measure Information:
Title
Percentage of patients that can avoid axillary lymph node dissection
Description
Percentage of patients that can achieve nodal pathological complete response after neoadjuvant chemotherapy
Time Frame
up to 4 weeks
Title
Percentage of successful magnetic seed guided lumpectomy
Description
Percentage of involved or close margins in lumpectomy specimen which require re-excision
Time Frame
up to 4 weeks
Title
Level of satisfaction from surgeons and radiologists
Description
Level of satisfaction from surgeons and radiologists which will be determined by the satisfaction questionnaire
Time Frame
To be filled in by operating surgeons and radiologists at the time of operation or magnetic seeds placement
Title
5-year local regional recurrence rate
Description
5-year ipsilateral breast tumor recurrence rate and/or axillary recurrence rate
Time Frame
5-year post-operatively

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All patients with cT1-3N1 invasive ductal carcinoma planned for neoadjuvant chemotherapy and/or target therapy mentally competent to give informed consent Agreed to proceed with curative operation after chemotherapy and tentatively keen for breast conservative surgery and targeted axillary dissection after neoadjuvant chemotherapy Radiologically 1-3 ipsilateral axillary lymph node metastases confirmed by cytology or biopsy Exclusion Criteria: Presence of distant metastasis, inflammatory breast cancers, multi-centric breast cancers History of previous ipsilateral axillary surgery or irradiation Hypersensitivity to dextran compounds or iron Iron overload disease Pregnant or lactating patients Patients with pacemaker or other implantable metallic devices in chest wall or prosthesis in shoulder Mentally incompetent patients
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Chi Mei Vivian Man, FCSHK, FRCSEd
Phone
852-25898116
Email
vivian27@hku.hk
First Name & Middle Initial & Last Name or Official Title & Degree
Christine Chan, Miss
Phone
852-2255 4773
Email
tcc0525@hku.hk
Facility Information:
Facility Name
University of Hong Kong
City
Hong Kong
Country
Hong Kong
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Christine Chan
Phone
852-22554765
Email
tcc0525@hku.hk
First Name & Middle Initial & Last Name & Degree
Candy
Phone
852-22554773
Email
kakai@hku.hk

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Magnetic Marker Localization for Occult Breast Cancer and Target Axillary Dissection in Node-positive Breast Cancer Post-neoadjuvant Chemotherapy

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