» Articles » PMID: 38942987

A Population-based Study on Trajectories of HER2 Status During Neoadjuvant Chemotherapy for Early Breast Cancer and Metastatic Progression

Overview
Journal Br J Cancer
Specialty Oncology
Date 2024 Jun 28
PMID 38942987
Authors
Affiliations
Soon will be listed here.
Abstract

Background: This study aimed to investigate the distribution and changes of HER2 status in untreated tumours, in residual disease and in metastasis, and their long-term prognostic implications.

Methods: This is a population-based cohort study of patients treated with neoadjuvant chemotherapy for breast cancer during 2007-2020 in the Stockholm-Gotland region which comprises 25% of the entire Swedish population. Information was extracted from the National Breast Cancer Registry and electronic patient charts to minimize data missingness and misclassification.

Results: In total, 2494 patients received neoadjuvant chemotherapy, of which 2309 had available pretreatment HER2 status. Discordance rates were 29.9% between primary and residual disease (kappa = 0.534), 31.2% between primary tumour and metastasis (kappa = 0.512) and 33.3% between residual disease to metastasis (kappa = 0.483). Adjusted survival curves differed between primary HER2 0 and HER2-low disease (p < 0.001), with the former exhibiting an early peak in risk for death which eventually declined below the risk of HER2-low. Across all disease settings, increasing the number of biopsies increased the likelihood of detecting HER2-low status.

Conclusion: HER2 status changes during neoadjuvant chemotherapy and metastatic progression, and the long-term behaviours of HER2 0 and HER2-low disease differ, underscoring the need for obtaining tissue biopsies and for extended follow-up in breast cancer studies.

Citing Articles

Clinical characteristics, metastasis patterns, and treatment outcomes of HER2-low breast cancer.

Lacruz M, Thies S, Schmidt-Pokrzywniak A, Wittenberg I, Engler T, Reinwald F Sci Rep. 2025; 15(1):4584.

PMID: 39920241 PMC: 11805968. DOI: 10.1038/s41598-025-88394-6.

References
1.
Peiffer D, Zhao F, Chen N, Hahn O, Nanda R, Olopade O . Clinicopathologic Characteristics and Prognosis of ERBB2-Low Breast Cancer Among Patients in the National Cancer Database. JAMA Oncol. 2023; 9(4):500-510. PMC: 9951099. DOI: 10.1001/jamaoncol.2022.7476. View

2.
Lindstrom L, Karlsson E, Wilking U, Johansson U, Hartman J, Lidbrink E . Clinically used breast cancer markers such as estrogen receptor, progesterone receptor, and human epidermal growth factor receptor 2 are unstable throughout tumor progression. J Clin Oncol. 2012; 30(21):2601-8. DOI: 10.1200/JCO.2011.37.2482. View

3.
Denkert C, Seither F, Schneeweiss A, Link T, Blohmer J, Just M . Clinical and molecular characteristics of HER2-low-positive breast cancer: pooled analysis of individual patient data from four prospective, neoadjuvant clinical trials. Lancet Oncol. 2021; 22(8):1151-1161. DOI: 10.1016/S1470-2045(21)00301-6. View

4.
Fernandez A, Liu M, Bellizzi A, Brock J, Fadare O, Hanley K . Examination of Low ERBB2 Protein Expression in Breast Cancer Tissue. JAMA Oncol. 2022; 8(4):1-4. PMC: 8814969. DOI: 10.1001/jamaoncol.2021.7239. View

5.
Liu X, Pawitan Y, Clements M . Parametric and penalized generalized survival models. Stat Methods Med Res. 2016; 27(5):1531-1546. DOI: 10.1177/0962280216664760. View