TY - JOUR
T1 - Survival outcomes of patients with HER2/neu-positive breast cancer with germline BRCA mutations
AU - Akkoc Mustafayev, Fatma Nihan
AU - Shukla, Mihir Amitabh
AU - Lanier, Amanda
AU - Milton, Denái R.
AU - Gutierrez, Angelica M.
AU - Gruschkus, Stephen K.
AU - Lewis, John E.
AU - Murthy, Rashmi K.
AU - Arun, Banu K.
N1 - Publisher Copyright:
© 2023 American Cancer Society.
PY - 2024/5/1
Y1 - 2024/5/1
N2 - Background: Breast cancer (BC) with germline BRCA1/2 mutations and their association with triple-negative BC has been thoroughly investigated. However, some carriers of BRCA1/2 mutations have human epidermal growth factor receptor 2 (HER2/neu)-positive BC, which has a different targeted therapy approach, and data are scarce for this patient population. The authors sought to characterize the clinical characteristics and outcomes of patients with HER2/neu-positive BC who had germline BRCA1/2 mutations. Methods: This was a retrospective analysis of data from 1099 patients diagnosed with HER2/neu-positive BC who were screened for germline BRCA mutations between 1996 and 2022. Clinicopathologic features and survival rates were analyzed by BRCA mutation status. Univariate and multivariable Cox proportional hazards regression models were used to analyze the association between clinical variables and outcomes. Results: Of 1099 patients with HER2/neu-positive BC, 73 (6.6%) tested positive for BRCA1/2 mutations. Age, race, and tumor characteristics did not differ between BRCA noncarriers and carriers. At a median follow-up of 78.6 months, the 5-year recurrence-free survival rate was 85% in BRCA carriers and 87% in noncarriers (p =.79), and the 5-year overall survival rate was 94% in BRCA carriers and 94% in noncarriers (p =.78). In a multivariable model, BRCA was not associated with recurrence-free survival (hazard ratio, 0.99; 95% confidence interval, 0.51–1.90; p =.96) or overall survival (hazard ratio, 0.83; 95% confidence interval, 0.33–2.07; p =.69). Conclusions: BRCA1/2 mutations occurred in 6.6% of patients with HER2/neu-positive BC and did not affect survival outcomes. Assessing the potential benefits of new treatment strategies, such as combining anti-HER2/neu therapies with poly(ADP-ribose) polymerase inhibitors, may lead to enhanced outcomes for these patients.
AB - Background: Breast cancer (BC) with germline BRCA1/2 mutations and their association with triple-negative BC has been thoroughly investigated. However, some carriers of BRCA1/2 mutations have human epidermal growth factor receptor 2 (HER2/neu)-positive BC, which has a different targeted therapy approach, and data are scarce for this patient population. The authors sought to characterize the clinical characteristics and outcomes of patients with HER2/neu-positive BC who had germline BRCA1/2 mutations. Methods: This was a retrospective analysis of data from 1099 patients diagnosed with HER2/neu-positive BC who were screened for germline BRCA mutations between 1996 and 2022. Clinicopathologic features and survival rates were analyzed by BRCA mutation status. Univariate and multivariable Cox proportional hazards regression models were used to analyze the association between clinical variables and outcomes. Results: Of 1099 patients with HER2/neu-positive BC, 73 (6.6%) tested positive for BRCA1/2 mutations. Age, race, and tumor characteristics did not differ between BRCA noncarriers and carriers. At a median follow-up of 78.6 months, the 5-year recurrence-free survival rate was 85% in BRCA carriers and 87% in noncarriers (p =.79), and the 5-year overall survival rate was 94% in BRCA carriers and 94% in noncarriers (p =.78). In a multivariable model, BRCA was not associated with recurrence-free survival (hazard ratio, 0.99; 95% confidence interval, 0.51–1.90; p =.96) or overall survival (hazard ratio, 0.83; 95% confidence interval, 0.33–2.07; p =.69). Conclusions: BRCA1/2 mutations occurred in 6.6% of patients with HER2/neu-positive BC and did not affect survival outcomes. Assessing the potential benefits of new treatment strategies, such as combining anti-HER2/neu therapies with poly(ADP-ribose) polymerase inhibitors, may lead to enhanced outcomes for these patients.
KW - BRCA1
KW - BRCA2
KW - breast cancer
KW - germline mutation
KW - human epidermal growth factor receptor 2 (HER2/neu)
UR - http://www.scopus.com/inward/record.url?scp=85179715155&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85179715155&partnerID=8YFLogxK
U2 - 10.1002/cncr.35159
DO - 10.1002/cncr.35159
M3 - Article
C2 - 38100492
AN - SCOPUS:85179715155
SN - 0008-543X
VL - 130
SP - 1600
EP - 1608
JO - Cancer
JF - Cancer
IS - 9
ER -