4.5 Article

Radio-frequency identification (RFID) tag localisation of non-palpable breast lesions a single centre experience

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BREAST
卷 69, 期 -, 页码 417-421

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CHURCHILL LIVINGSTONE
DOI: 10.1016/j.breast.2023.04.005

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Localisation; RFID; Non -palpable; Breast cancer

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This study aimed to report the surgical experience and outcomes of pre-operative localisation of non-palpable breast lesions using the RFID tag system. The results showed that the RFID tag system has been effective in accurately locating breast lesions in recent years.
Aim: The purpose of this study is to report the surgical experience and outcomes with pre-operative localisation of non-palpable breast lesions using the RFID tag system.Methods: The cohort for this prospective study included patients over the age of 18 with biopsy proven, non -palpable indeterminate lesions, DCIS or breast cancer requiring pre-operative localisation before surgical exci-sion between September 2020 and July 2022.Results: A total of 312 RFID tags were placed in 299 consecutive patients. Indications for localisation included non-palpable invasive cancer in 255 (85.3%) patients, in situ disease in 38 (12.7%) and indeterminate lesions requiring surgical excision in 6 (2.0%). Both in situ and invasive lesions had a median size of 13 mm (range 4-100 mm) on pre-operative imaging. The RFID tags were in situ for a median time of 21 days before surgery (range 0-233 days). Of the 213 tags, 292 (93.6%) were introduced using ultrasound (USS) guidance and ster-eotactically in 20 (6.4%). In 3 (1.0%) cases the RFID tag was either not satisfactorily deployed at the intended target or retrieved intra-operatively. Following discussion of post-operative histology by the multi-disciplinary team, further surgery for close or involved margins was for 26 (8.7%) patients.Conclusion: The Hologic RFID tag system can be used for accurate pre-operative localisation of non-palpable masses as well as diffuse abnormalities such as mammographic distortions and calcifications. It has advan-tages of flexibility for scheduling image-guided insertion independently of scheduled operating lists and can be placed to localise lesions prior to initiating neoadjuvant systemic treatment.

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