Discordance of Biomarker Expression Profile between Primary Breast Cancer and Synchronous Axillary Lymph Node Metastasis in Preoperative Core Needle Biopsy

Author:

Marletta Stefano12ORCID,Giorlandino Alexandra3ORCID,Cavallo Enrico1,Dello Spedale Venti Michele1ORCID,Leone Giorgia1,Tranchina Maria Grazia1,Gullotti Lucia1,Bonanno Claudia Lucia1,Spoto Graziana1,Falzone Giusi1,Tornabene Irene1,Trovato Carmelina1,Baron Marco Maria1,Di Mauro Giuseppe1,Falsaperna Lucia1,Angelico Giuseppe4ORCID,Pafumi Sarah56,Rizzo Antonio1

Affiliation:

1. Division of Pathology, Humanitas Istituto Clinico Catanese, 95045 Catania, Italy

2. Department of Diagnostics and Public Health, Section of Pathology, University of Verona, 37134 Verona, Italy

3. Pathology Unit, ARNAS Garibaldi Hospital, 95122 Catania, Italy

4. Department of Medical, Surgical Sciences and Advanced Technologies G.F. Ingrassia, Anatomic Pathology, University of Catania, 95125 Catania, Italy

5. Medical Oncology, Humanitas Istituto Clinico Catanese, 95045 Catania, Italy

6. Section of Oncology, Department of Medicine, University of Verona, Verona University Hospital Trust (AUOI), 37124 Verona, Italy

Abstract

Background: Breast cancer (BC) is a heterogeneous disease made up of clones with different metastatic potential. Intratumoral heterogeneity may cause metastases to show divergent biomarker expression, potentially affecting chemotherapy response. Methods: We investigated the immunohistochemical (IHC) and FISH profile of estrogen receptors (ER), progesterone (PR) receptors, Ki67, and HER2 in a series of BC-matched primary tumors (PTs) and axillary lymph node (ALN) metastases in pre-operative core needle biopsies (CNBs). Phenotypical findings were correlated to morphological features and their clinical implications. Results: Divergent expression between PTs and ALNs was found in 10% of the tumors, often involving multiple biomarkers (12/31, 39%). Most (52%) displayed significant differences in ER and PR staining. HER2 divergences were observed in almost three-quarters of the cases (23/31, 74%), with five (16%) switching from negativity to overexpression/amplification in ALNs. Roughly 90% of disparities reflected significant morphological differences between PTs and ALN metastases. Less than half of the discrepancies (12/31, 39%) modified pre/post-operative treatment options. Conclusions: We observed relevant discrepancies in biomarker expression between PTs and metastatic ALNs in a noteworthy proportion (10%) of preoperative BC CNBs, which were often able to influence therapies. Hence, our data suggest routine preoperative assessment of biomarkers in both PTs and ALNs in cases showing significant morphological differences.

Publisher

MDPI AG

Subject

Clinical Biochemistry

Reference42 articles.

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