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Distance of Biopsy-Confirmed High-Risk Breast Lesion from Concurrently Identified Breast Malignancy Associated with Risk of Carcinoma at the High-Risk Lesion Siteopen access

Authors
Le, JulieO'Keefe, Thomas J.Khan, SohiniGrossi, Sara M.Choi, Hye YoungOjeda-Fournier, HaydeeArmani, AvaWallace, Anne M.Blair, Sarah L.
Issue Date
Jun-2024
Publisher
Multidisciplinary Digital Publishing Institute (MDPI)
Keywords
breast cancer; high-risk breast lesion; synchronous breast cancer; intraductal papilloma; complex sclerosing lesion of breast; lobular hyperplasia; flat epithelial atypia
Citation
Cancers, v.16, no.12
Indexed
SCIE
SCOPUS
Journal Title
Cancers
Volume
16
Number
12
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/71028
DOI
10.3390/cancers16122268
ISSN
2072-6694
2072-6694
Abstract
Simple Summary Incidental intraductal papilloma without atypia (IPA), lobular hyperplasia (LCIS or ALH), flat epithelial atypia (FEA) and complex sclerosing lesion (CSL) are high-risk lesions of the breast. These lesions are not routinely excised when diagnosed in isolation because they have low rates of upgrade to invasive cancer. When identified concurrently with invasive breast cancer, however, the upgrade rate is not well characterized. We sought to both characterize the upgrade rate for these lesions when diagnosed concurrently with invasive breast cancer, and to identify features of the high-risk lesions predictive of upgrade to cancer. In our cohort of 65 patients who were concurrently diagnosed with a high-risk breast lesion and an invasive cancer, 5 patients (7.7%) had an upgrade of their high-risk lesion to carcinoma. The rate of upgrade was higher for high-risk lesions that were ipsilateral to malignancy and within 5 cm of it, and lower for other lesions.Abstract High-risk breast lesions including incidental intraductal papilloma without atypia (IPA), lobular hyperplasia (LCIS or ALH), flat epithelial atypia (FEA) and complex sclerosing lesion (CSL) are not routinely excised due to low upgrade rates to carcinoma. We aim to identify features of these lesions predictive of upgrade when identified concurrently with invasive disease. Methods: A single-center retrospective cohort study was performed for patients who underwent multi-site lumpectomies with invasive disease at one site and a high-risk lesion at another site between 2006 and 2021. A multinomial logistic regression was performed. Results: Sixty-five patients met the inclusion criteria. Four patients (6.2%) had an upgrade to in situ disease (DCIS) and one (1.5%) to invasive carcinoma. Three upgraded high-risk lesions were ipsilateral to the concurrent carcinoma and two were contralateral. In the multivariate model, a high-risk lesion within 5 cm of an ipsilateral malignancy was associated with increased risk of upgrade. The 3.8% upgrade rate for high-risk lesions located greater than 5 cm from ipsilateral malignancy or in the contralateral breast suggests that omission of excisional biopsy may be considered. Excisional biopsy of lesions within 5 cm of ipsilateral malignancy is recommended given the 25% upgrade risk in our series.
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