Back to Search Start Over

HER2DX ERBB2 mRNA expression in advanced HER2-positive breast cancer treated with T-DM1.

Authors :
Brasó-Maristany F
Griguolo G
Chic N
Pascual T
Paré L
Maues J
Galván P
Dieci MV
Miglietta F
Giarratano T
Martínez-Sáez O
Marín-Aguilera M
Schettini F
Conte B
Angelats L
Vidal M
Adamo B
Muñoz M
Sanfeliu E
González B
Vivancos A
Villagrasa P
Parker JS
Perou CM
Conte P
Prat A
Guarneri V
Source :
Journal of the National Cancer Institute [J Natl Cancer Inst] 2023 Mar 09; Vol. 115 (3), pp. 332-336.
Publication Year :
2023

Abstract

In advanced HER2-positive (HER2+) breast cancer, the new antibody-drug conjugate trastuzumab deruxtecan is more effective compared with trastuzumab emtansine (T-DM1). However, trastuzumab deruxtecan can have considerable toxicities, and the right treatment sequence is unknown. Biomarkers to guide the use of anti-HER2 therapies beyond HER2 status are needed. Here, we evaluated if preestablished levels of ERBB2 mRNA expression according to the HER2DX standardized assay are associated with response and survival following T-DM1. In ERBB2 low, medium, and high groups, the overall response rate was 0%, 29%, and 56%, respectively (P < .001). ERBB2 mRNA was statistically significantly associated with better progression-free survival (P = .002) and overall survival (OS; P = .02). These findings were independent of HER2 immunohistochemistry (IHC) levels, hormone receptor, age, brain metastasis, and line of therapy. The HER2DX risk score (P = .04) and immunoglobulin signature (P = .04) were statistically significantly associated with overall survival since diagnosis. HER2DX provides prognostic and predictive information following T-DM1 in advanced HER2+ breast cancer.<br /> (© The Author(s) 2022. Published by Oxford University Press. All rights reserved. For permissions, please email: journals.permissions@oup.com.)

Details

Language :
English
ISSN :
1460-2105
Volume :
115
Issue :
3
Database :
MEDLINE
Journal :
Journal of the National Cancer Institute
Publication Type :
Academic Journal
Accession number :
36576009
Full Text :
https://doi.org/10.1093/jnci/djac227