Racial and ethnic disparities in clinical outcomes of HER2-positive metastatic breast cancer treated with antibody-drug conjugates.

Authors

Zunairah Shah, Lan Lei, Rahul Thakur, Ajinkya Buradkar, Malak Alharbi, Mulham Ombada, Song Yao, Alfredo Chua, Han Yu, Sunil Badve, Thaer Khoury, Anant Madabhushi, Ujjwal Baid, Kevin Kalinsky, Sheheryar Kabraji, Shipra Gandhi

Published in

Journal of the National Cancer Institute. Jul 07, 2026. Epub Jul 07, 2026.

Abstract

Antibody-drug conjugates (ADCs) have substantially improved outcomes for patients with HER2-positive (HER2+) metastatic breast cancer (MBC). Whether these survival gains have translated equitably across racial and ethnic groups remains unclear despite persistent disparities in breast cancer outcomes.
We conducted a retrospective cohort study using de-identified electronic health record data from the TriNetX Research Network (2010 to 2024). Adults with HER2+ MBC treated with trastuzumab deruxtecan (T-DXd) or trastuzumab emtansine (T-DM1) were included. Overall survival (OS) was estimated using Kaplan-Meier methods and compared across racial and ethnic groups. Multivariable Cox models adjusted for age, body mass index, chronic obstructive pulmonary disease, hypertension, diabetes mellitus, and prior lines of therapy.
The cohort included 7,462 patients with HER2+ MBC: 5,072 non-Hispanic White (NHW) (68%), 1,193 Black (16%), 746 Hispanic (10%), and 298 Asian (4%). Five-year OS was highest among Asian (89.9%) and Hispanic (86.3%) patients, followed by NHW (84.0%) and Black patients (80.3%) (P < .001). Compared with NHW patients, Black patients experienced significantly worse OS (adjusted HR, 1.22; 95% CI, 1.03 to 1.45; P=.03). Survival differences among Asian and Hispanic patients were not significant after multivariable adjustment.
Among patients with HER2+ MBC treated with HER2-directed ADCs, Black patients experienced persistently inferior survival despite receipt of effective therapies. These findings highlight ongoing inequities and underscore the need for interventions to ensure equitable translation of therapeutic advances across all populations.

PMID:
42411768
Bibliographic data and abstract were imported from PubMed on 07 Jul 2026.

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