Prognostic significance of EGFR, MUC1 and PD-L1 expressions in cases with triple negative breast cancer.


Journal

Journal of B.U.ON. : official journal of the Balkan Union of Oncology
ISSN: 2241-6293
Titre abrégé: J BUON
Pays: Cyprus
ID NLM: 100883428

Informations de publication

Date de publication:
Historique:
entrez: 12 4 2020
pubmed: 12 4 2020
medline: 22 12 2020
Statut: ppublish

Résumé

Twenty percent of the breast cancers are triple negative (TNBC). Despite the impressive progression in the biology of this subgroup, data is limited as compared to hormone and/or HER2 positive cases. Thus, the aim of this study was to detect the expression levels and to identify the prognostic values of MUC1, EGFR and PD-L1 in TNBC. MUC1, EGFR and PD-L1 expressions were detected by immunohistochemistry in 97 cases with TNBC. Associations between clinical and histopathological parameters with overall survival (OS) and progression-free survival (PFS) were analyzed using the Kaplan-Meier method and compared by the log-rank test. Prognostic effects were analyzed by Cox proportional hazard models. During a median follow-up of 93 months (0.6-168.7) the mean PFS was 110.1 and OS was 121.8 months. Tumor diameter (T), involved lymph node status (N) and TNM were found to be prognostic for PFS and OS. PD-L1 in microenvironment (PD-L1 ME) and EGFR expression were found to be associated with longer PFS and OS, but MUC1 and tumor PD-L1 (PD-L1 TM) expressions were not. All combined analyses showed that in the subgroups of MUC1, PD-L1 TM or ME positive, EGFR expression was correlated with longer PFS and OS than those who were not. Older age (≥70 years), T and N status and also EGFR expression were found to be independent prognostic factors for OS in Cox regression analysis. EGFR expression was found to be one of the most important prognostic factors in addition to T and N status in cases with TNBC.

Identifiants

pubmed: 32277627

Substances chimiques

B7-H1 Antigen 0
CD274 protein, human 0
MUC1 protein, human 0
Mucin-1 0
EGFR protein, human EC 2.7.10.1
ErbB Receptors EC 2.7.10.1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

159-167

Auteurs

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Classifications MeSH