Localization of Nonpalpable Breast Lesions
Breast Cancer, Carcinoma in Situ
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
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
Experimental
Active Comparator
Radioactive seed localization (RSL)
Wire-guided localization (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 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.