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A Trial of RSL Versus WL for Malignant Breast Disease (BCS-RSL-001)

Wake Forest University (WFU) logo

Wake Forest University (WFU)

Status

Completed

Conditions

Breast- Female

Treatments

Procedure: Wire Localization
Procedure: Radioactive Seed Localization

Study type

Interventional

Funder types

Other

Identifiers

NCT02522468
LCI-BRE-BCS-RSL-001

Details and patient eligibility

About

The purpose of this randomized trial is to determine the superiority of utilizing radioactive seed localization (RSL) over wire-guided localization (WL) for palpable or non-palpable malignant lesions in patients undergoing breast conservation surgery (BCS).

Full description

Consented and eligible subjects will be randomized to either radioactive seed localization or wire localization and stratified by surgeon and invasive versus DCIS prior to localization. Subjects on both arms will undergo breast conservation surgery including surgical specimen removal. Specimens will be grossed according to standard of care procedures. Localization, breast conservation surgery, and post-operative appointments will follow standard of care guidelines. Surveys will be administered according to the study calendar to the radiologist, surgeon, pathologist, and subject for data collection.

Enrollment

400 patients

Sex

Female

Ages

20 to 99 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Female
  • 20 to 99 years of age
  • Breast lesion necessitating image-guided excision
  • Unifocal disease
  • Breast-conservation candidate
  • Biopsy-proven malignant breast lesion including by not limited to invasive ductal carcinoma, invasive lobular carcinoma, and ductal carcinoma in situ
  • Signed written informed consent document by the subject and/or a LAR

Exclusion criteria

  • Male
  • Multifocal or multicentric disease
  • Receiving neoadjuvant chemotherapy
  • Pregnant or breastfeeding
  • Locally advanced disease
  • Breast conservation contraindication such as inability to receive whole breast radiation therapy, inability to tolerate localization procedure, inability to lay flat or prone for radiation, and undesirable tumor to breast ratio
  • Prior breast cancer on ipsilateral side
  • Unable or unwilling to adhere to post-localization instructions (e.g. timely seed removal)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

400 participants in 2 patient groups

Radioactive Seed Localization
Experimental group
Description:
Radioactive Seeds
Treatment:
Procedure: Radioactive Seed Localization
Wire Localization
Active Comparator group
Description:
Wire
Treatment:
Procedure: Wire Localization

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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