Comparing the HER2 Status of the Primary Tumor to That of Disseminated Tumor Cells in Early Breast Cancer.
breast cancer
disseminated tumor cells
minimal residual disease
targeted therapy
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
29 May 2024
29 May 2024
Historique:
received:
10
04
2024
revised:
21
05
2024
accepted:
26
05
2024
medline:
19
6
2024
pubmed:
19
6
2024
entrez:
19
6
2024
Statut:
epublish
Résumé
Breast cancer remains a leading cause of cancer mortality in women globally. Despite advancements in systemic therapy, the risk of distant recurrence persists even after such treatment and may be linked to disseminated tumor cells (DTCs). Variability in molecular characteristics between primary tumors (PTs) and distant metastases underscores the need to comprehensively understand metastatic pathways. This retrospective study investigated discrepancies between HER2 expression in PTs and DTCs and their implications for survival outcomes in 201 early breast cancer (EBC) patients. We found a significant association between HER2 expression in PTs and DTCs when classifying tumors as HER2-high/low/negative. Patients whose HER2 status was discordant between PTs and DTCs exhibited worse distant disease-free survival than those with concordant status. Multivariate analysis confirmed the HER2 status of DTCs as an independent prognostic factor for distant DFS. These findings emphasize the importance of assessing HER2 expression in DTCs and its potential implications for tailored therapy strategies in EBC. Furthermore, prospective trials are needed to validate these findings and explore targeted therapies based on the molecular characteristics of DTCs.
Identifiants
pubmed: 38892097
pii: ijms25115910
doi: 10.3390/ijms25115910
pii:
doi:
Substances chimiques
Receptor, ErbB-2
EC 2.7.10.1
ERBB2 protein, human
EC 2.7.10.1
Biomarkers, Tumor
0
Types de publication
Journal Article
Comparative Study
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : This study was financially supported by the German Cancer Aid (Priority Program 'Translational Oncology: DETECT-CTC-HIGH'; Project-ID: 70114705).The work described in this paper was conducted in the framework of the Graduate School 2543/1 "Intraoperative
ID : This study was financially supported by the German Cancer Aid (Priority Program 'Translational Oncology: DETECT-CTC-HIGH'; Project-ID: 70114705).The work described in this paper was conducted in the framework of the Graduate School 2543/1 "Intraoperative