Abstract PS4-12-12: Racial Disparities in Pathologic Complete Response in Patients with HER2 Positive Breast Cancer Treated with Neoadjuvant Chemotherapy
Abstract
Abstract Background: Black patients with human epidermal growth factor receptor 2 (HER2)-positive breast cancers have lower rates of pathologic complete response (pCR) following neoadjuvant chemotherapy (NAC). This study aims to identify factors that contribute to disparities in achieving a pCR in HER2-positive breast cancers. Method: A retrospective review of an institutional tumor registry identified women with HER2-positive breast cancers who underwent NAC followed by surgery from 2016 to 2022. Sociodemographic factors, clinicopathologic features, and treatment variables were compared between patients self-identified as Black, White, and Other. Results: The study included 445 women with a median age of 54 (range 22-86) and a median follow-up of 48 months (range 7-110). A total of 355 (79.8%) self-identified as White, 58 (13.0%) Black, and 32 (7.2%) Other. There were no differences in Charlson Comorbidity Index, type of insurance, hormone receptor status, HER2 immunohistochemical score, clinical stage, overall grade, chemotherapy regimen, and completion of chemotherapy between racial groups. There was no difference in median number of days from diagnosis to initiation of chemotherapy or median number of days from completion of chemotherapy to surgery between racial groups (Black = 30.5, White = 30, Other = 31.5 [p=0.85] and Black = 22, White, 19, Other = 21 [p=0.26]). Following NAC, Black patients achieved a pCR in both the breast and axilla less frequently than White patients or Other (24 [41%] Black patients, 191 [54%] White patients, 20 [63%] Other), although this difference was not statistically significant (p=0.11). Factors associated with achieving pCR included age of diagnosis
Fields of Study & Subjects
Breast Cancer Treatment Studies
HER2/EGFR in Cancer Research
Gastric Cancer Management and Outcomes
Publication details
- Journal / source
- Clinical Cancer Research
- Volume
- 32
- Issue
- 4_Supplement
- Pages
- PS4–12
- Publication date
- 17 February 2026
- Language
- EN