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Localization of Nonpalpable Breast Lesions

Primary Purpose

Breast Cancer, Carcinoma in Situ

Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Radioactive seed localization (RSL)
Wire-guided localization (WGL)
Sponsored by
Rigshospitalet, Denmark
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Breast Cancer focused on measuring Nonpalpable breast lesions, Breast Cancer and carcinoma in situ, Radioactive seed localization, Wire-guided localization, Randomized study

Eligibility Criteria

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

Inclusion Criteria:

  • Patients with nonpalpable breast lesions, carcinoma in situ or invasive carcinoma, where preoperative lesion localization is necessary.
  • All age groups, minimum 18 years

Exclusion criteria:

  • Patients with benign nonpalpable breast lesions.
  • Patients who are unable to comprehend the information.
  • Patients who are pregnant, breastfeeding or have children < 3 years.
  • Patients who have lesions, which requires more than two wires or seeds for localization.

Sites / Locations

  • Rigshospitalet (Copenhagen University Hospital)

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Radioactive seed localization (RSL)

Wire-guided localization (WGL)

Arm Description

Patients are randomised for preoperative lesion localization with either radioactive seed localization (RSL) or wire-guided localization (WGL). In this arm 205 patients will have RSL performed. The radioactive seed is introduced through a gauge needle using standard ultrasound guidance. Once guided to the nonpalpable breast lesion, the seed is deployed into the breast tissue by advancing a stilette in the needle. The exact location is confirmed by mammography. The nonpalpable lesion is located during the operation with a handheld gamma probe, identical to the one used for the sentinel node procedure. The surgical specimen is orientated and examined at the Department of Radiology and Pathology in accordance with the existing guidelines of WGL.

Patients are randomised for preoperative lesion localization with either radioactive seed localization (RSL) or wire-guided localization (WGL). In this arm 205 patients will have WGL performed. Guided by ultrasound or mammography a flexible wire is introduced into the breast by the radiologist just before the operation. The tip of the wire must mark the nonpalpable lesion, and correct localization is verified by mammography. The surgeon uses the wire and mammography as a guide during the operation. The surgical specimen is orientated and examined at the Department of Radiology and Pathology in accordance with the existing guidelines of WGL.

Outcomes

Primary Outcome Measures

Re-operation rate due to positive microscopic margins detected at the final pathological evaluation.

Secondary Outcome Measures

Amount of excised breast tissue in relation to tumour size.

Full Information

First Posted
July 14, 2013
Last Updated
August 9, 2017
Sponsor
Rigshospitalet, Denmark
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1. Study Identification

Unique Protocol Identification Number
NCT01901991
Brief Title
Localization of Nonpalpable Breast Lesions
Official Title
A Randomized Study of Localization of Nonpalpable Breast Lesions - RSL vs WGL
Study Type
Interventional

2. Study Status

Record Verification Date
September 2016
Overall Recruitment Status
Completed
Study Start Date
January 2014 (undefined)
Primary Completion Date
February 2016 (Actual)
Study Completion Date
February 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rigshospitalet, Denmark

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Each year the Danish mammography-screening programme identifies a large number of patients with small non-palpable breast cancers or precancerous lesions. The majority of these patients are suitable for breast conserving surgery (BCS). The object of BCS is to remove the suspicious lesion completely without removing excess healthy breast tissue. To obtain this accurate lesion localization is essential. Until today the standard procedure in Denmark has been wire guided localization (WGL). Although the method has been utilized for a number of years it has several disadvantages. Often inaccurate lesion localization leads to incomplete lesion removal (positive margin) and subsequently reoperation. It can postpone the additional systemic treatment, offered after the operation. Other disadvantages are poor cosmetic outcome and inconvenient planning for the patient and the departments involved. The wire needs to be placed on the day of the operation, which decreases the flexibility of the procedure. The purpose of this study is to test a new method named radioactive seed localization (RSL). The method uses a small titanium seed containing radioactive iodine. It will be placed in the centre of the lesion, and during the operation, the surgeon can locate it with a handheld gamma probe. The seed can be placed a few days in advance, which means a more flexible course of treatment. The method seems promising with regards to reoperation rates, but it needs further testing. Hypothesis: RSL is a more accurate method, for localization of nonpalpable breast lesions, than WGL. Using RSL obtains, to a great extent, adequate negative margins, resulting in a reduced number of re-operations. The study will be performed as a randomised clinical trial, where the two methods will be compared to each other. The trial will be performed at the department of breast surgery at Rigshospitalet and include patients with nonpalpable breast lesions. Besides reoperation rates, duration of the surgical procedure and the amount of removed breast tissue will be compared.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer, Carcinoma in Situ
Keywords
Nonpalpable breast lesions, Breast Cancer and carcinoma in situ, Radioactive seed localization, Wire-guided localization, Randomized study

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
410 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Radioactive seed localization (RSL)
Arm Type
Experimental
Arm Description
Patients are randomised for preoperative lesion localization with either radioactive seed localization (RSL) or wire-guided localization (WGL). In this arm 205 patients will have RSL performed. The radioactive seed is introduced through a gauge needle using standard ultrasound guidance. Once guided to the nonpalpable breast lesion, the seed is deployed into the breast tissue by advancing a stilette in the needle. The exact location is confirmed by mammography. The nonpalpable lesion is located during the operation with a handheld gamma probe, identical to the one used for the sentinel node procedure. The surgical specimen is orientated and examined at the Department of Radiology and Pathology in accordance with the existing guidelines of WGL.
Arm Title
Wire-guided localization (WGL)
Arm Type
Active Comparator
Arm Description
Patients are randomised for preoperative lesion localization with either radioactive seed localization (RSL) or wire-guided localization (WGL). In this arm 205 patients will have WGL performed. Guided by ultrasound or mammography a flexible wire is introduced into the breast by the radiologist just before the operation. The tip of the wire must mark the nonpalpable lesion, and correct localization is verified by mammography. The surgeon uses the wire and mammography as a guide during the operation. The surgical specimen is orientated and examined at the Department of Radiology and Pathology in accordance with the existing guidelines of WGL.
Intervention Type
Procedure
Intervention Name(s)
Radioactive seed localization (RSL)
Intervention Description
Localization of nonpalpable breast lesions with Radioactive seed localization
Intervention Type
Procedure
Intervention Name(s)
Wire-guided localization (WGL)
Intervention Description
Localization of nonpalpable breast lesions with Wire-guided localization
Primary Outcome Measure Information:
Title
Re-operation rate due to positive microscopic margins detected at the final pathological evaluation.
Time Frame
Re-operation within 3 months after the initial breast conserving surgery.
Secondary Outcome Measure Information:
Title
Amount of excised breast tissue in relation to tumour size.
Time Frame
3 months.
Other Pre-specified Outcome Measures:
Title
Duration of the surgical procedure.
Time Frame
3 months.

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with nonpalpable breast lesions, carcinoma in situ or invasive carcinoma, where preoperative lesion localization is necessary. All age groups, minimum 18 years Exclusion criteria: Patients with benign nonpalpable breast lesions. Patients who are unable to comprehend the information. Patients who are pregnant, breastfeeding or have children < 3 years. Patients who have lesions, which requires more than two wires or seeds for localization.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Niels Kroman, Professor
Organizational Affiliation
Rigshospitalet (Copenhagen University Hospital), Department of Breast Surgery
Official's Role
Study Chair
Facility Information:
Facility Name
Rigshospitalet (Copenhagen University Hospital)
City
Copenhagen
State/Province
Østerbro
ZIP/Postal Code
2100
Country
Denmark

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Data will be presented in a international peer review article.
Citations:
PubMed Identifier
28257326
Citation
Langhans L, Tvedskov TF, Klausen TL, Jensen MB, Talman ML, Vejborg I, Benian C, Roslind A, Hermansen J, Oturai PS, Bentzon N, Kroman N. Radioactive Seed Localization or Wire-guided Localization of Nonpalpable Invasive and In Situ Breast Cancer: A Randomized, Multicenter, Open-label Trial. Ann Surg. 2017 Jul;266(1):29-35. doi: 10.1097/SLA.0000000000002101.
Results Reference
result

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Localization of Nonpalpable Breast Lesions

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