The impact of HER2-directed targeted therapy on HER2-positive DCIS of the breast

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Abstract

Background: In invasive breast cancer, her2 is a well-established negative prognostic factor. however, its significance on the prognosis of ductal carcinoma in situ (DcIs) of the breast is unclear. as a result, the impact of her2-directed therapy on her2-positive DcIs is unknown and is currently the subject of ongoing clinical trials. In this study, we aim to determine the possible impact of her2-directed targeted therapy on survival outcomes for her2-positive DcIs patients. Materials and methods: The National cancer Data Base (NcDB) was used to retrieve patients with biopsy-proven DcIs diagnosed from 2004–2015. patients were divided into two groups based on the adjuvant therapy they received: systemic her2-directed targeted therapy or no systemic therapy. statistics included multivariable logistic regression to determine factors predictive of receiving systemic therapy, Kaplan-Meier analysis to evaluate overall survival (Os), and cox proportional hazards modeling to determine variables associated with Os. results: altogether, 1927 patients met inclusion criteria; 430 (22.3%) received her2-directed targeted therapy; 1497 (77.7%) did not. patients who received her2-directed targeted therapy had a higher 5-year Os compared to patients that did not (97.7% vs. 95.8%, p = 0.043). This survival benefit remained on multivariable analysis. Factors associated with worse Os on multivariable analysis included charlson-Deyo comorbidity score ≥ 2 and no receipt of hormonal therapy. conclusion: In this large study evaluating her2-positive DcIs patients, the receipt of her2-directed targeted therapy was associated with an improvement in Os. The results of currently ongoing clinical trials are needed to confirm this finding.

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Lewis, G. D., Haque, W., Farach, A., Hatch, S. S., Brian Butler, E., Niravath, P. A., … Teh, B. S. (2021). The impact of HER2-directed targeted therapy on HER2-positive DCIS of the breast. In Reports of Practical Oncology and Radiotherapy (Vol. 26, pp. 179–187). Via Medica. https://doi.org/10.5603/RPOR.a2021.0026

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