Aberrant expression of GATA3 in metastatic adenocarcinoma of the prostate: an important pitfall

Author:

Lobo João123ORCID,Tenace Nazario P4ORCID,Cañete‐Portillo Sofia5,Carneiro Isa12,Henrique Rui123,Lucianò Roberta4,Harik Lara R6,Magi‐Galluzzi Cristina5ORCID

Affiliation:

1. Department of Pathology Portuguese Oncology Institute of Porto (IPO Porto)/Porto Comprehensive Cancer Center Raquel Seruca (P.CCC) Porto Portugal

2. Cancer Biology and Epigenetics Group, IPO Porto Research Center (GEBC CI‐IPOP) Portuguese Oncology Institute of Porto (IPO Porto)/Porto Comprehensive Cancer Center Raquel Seruca (P.CCC) & RISE@CI‐IPOP (Health Research Network) Porto Portugal

3. Department of Pathology and Molecular Immunology ICBAS – School of Medicine and Biomedical Sciences, University of Porto Porto Portugal

4. Department of Pathology Università Vita‐Salute San Raffaele Milano Italy

5. Department of Pathology Heersink School of Medicine, The University of Alabama at Birmingham Birmingham AL USA

6. Department of Pathology and Laboratory Medicine Emory University School of Medicine Atlanta GA USA

Abstract

AimsThe distinction of high‐grade prostate cancer (PCa) from poorly differentiated urothelial carcinoma (UC) can be somewhat challenging on clinical and morphological grounds alone, yet it is of great importance for prognostication and choice of treatment. GATA3 is a useful immunohistochemical marker to confirm urothelial origin. However, recent works report strong GATA3 immunoexpression in primary high‐grade PCa. The aim of this study was to explore GATA3 expression specifically in metastatic PCa.Methods and resultsThe pathology databases of four tertiary institutions were queried for cases of metastatic PCa. Available slides and clinical records were reviewed by experienced genitourinary pathologists. Prostatic markers (PSA, PSAP, NKX3.1) and GATA3 immunohistochemistry were performed. A total of 163 metastatic PCa cases were included. At least one prostate marker was positive in each case of non‐regional distant metastasis, confirming prostatic origin. GATA3 strong staining was found in four (2.5%) cases: two liver, one bone and one non‐regional lymph‐node metastases. All four patients had Grade Group 5 PCa at the initial diagnosis. The metastatic prostatic adenocarcinomas were solid, either with no gland formation (n = 3) or with only focal cribriforming (n = 1).ConclusionsTo our knowledge, this is the first study exploring GATA3 expression specifically in metastatic PCa. Despite being infrequent, GATA3 positivity in high‐grade PCa may lead to misdiagnosis, with clinical implications. We recommend a panel of immunohistochemical markers, both prostatic and urothelial, for ruling out UC, either in primary tumour samples or in the event of metastases of unknown primary, when a genitourinary origin is suspected.

Publisher

Wiley

Subject

General Medicine,Histology,Pathology and Forensic Medicine

Reference39 articles.

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