The Clinical Significance of Neuroendocrine Features in Invasive Breast Carcinomas.


Journal

The oncologist
ISSN: 1549-490X
Titre abrégé: Oncologist
Pays: England
ID NLM: 9607837

Informations de publication

Date de publication:
09 2020
Historique:
received: 03 02 2020
accepted: 06 05 2020
pubmed: 31 5 2020
medline: 22 6 2021
entrez: 31 5 2020
Statut: ppublish

Résumé

The latest World Health Organization (WHO) classification categorized invasive breast carcinomas (IBCs) with neuroendocrine (NE) differentiations into neuroendocrine neoplasms (including well-differentiated neuroendocrine tumor [NET] and poorly differentiated neuroendocrine carcinoma [NEC]) and IBC no special type with NE features (IBC-NST-NE). However, little is documented of the clinical significance of this classification; also the precise thresholds and choices of NE markers were variable. In the current study, a large cohort of patients with IBC with NE differentiation were morphologically classified based on the WHO criteria and the clinical relevance of expression of different NE markers (synaptophysin [SYN], chromogranin [CG], and CD56) was evaluated. Among 1,372 IBCs, 52 NET (3.8%) and 172 IBC-NST-NE (12.5%) were identified. Compared with the IBC-no NE cases, NET and IBC-NST-NE were similarly associated with positive estrogen receptor (ER) expression and lower grade (p < .001). For patient outcome, IBC-NST-NE, but not NET, demonstrated significantly worse survival than the IBC-no NE cases. Based on high (≥50%) and low (<50%) expression for each NE marker, independent poor disease-free survival for SYN

Identifiants

pubmed: 32472950
doi: 10.1634/theoncologist.2020-0081
pmc: PMC7485343
doi:

Substances chimiques

Biomarkers, Tumor 0
Chromogranin A 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1318-e1329

Informations de copyright

© AlphaMed Press 2020.

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Auteurs

Billy Shui-Wun Lai (BS)

Department of Pathology, North District Hospital, Hong Kong.

Julia Y Tsang (JY)

Department of Anatomical and Cellular Pathology, Prince of Wales Hospital, The Chinese University of Hong Kong, Ngan Shing Street, Shatin, NT, Hong Kong.

Ivan K Poon (IK)

Department of Anatomical and Cellular Pathology, Prince of Wales Hospital, The Chinese University of Hong Kong, Ngan Shing Street, Shatin, NT, Hong Kong.

Yan Shao (Y)

Department of Anatomical and Cellular Pathology, Prince of Wales Hospital, The Chinese University of Hong Kong, Ngan Shing Street, Shatin, NT, Hong Kong.

Siu-Ki Chan (SK)

Department of Pathology, Kwong Wah Hospital, Hong Kong.

Fiona K Tam (FK)

Department of Pathology, Kwong Wah Hospital, Hong Kong.

Sai-Yin Cheung (SY)

Department of Pathology, Tuen Mun Hospital, Hong Kong.

Ka-Ho Shea (KH)

Department of Pathology, Tuen Mun Hospital, Hong Kong.

Gary M Tse (GM)

Department of Anatomical and Cellular Pathology, Prince of Wales Hospital, The Chinese University of Hong Kong, Ngan Shing Street, Shatin, NT, Hong Kong.

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