Evidence map›Paper›PMID 41053794›Full record

ArticleBMC women's health2025

Analysis of clinicopathological features and clinical significance in 25 cases of mammary adenoid cystic carcinoma.

Xiaoyan Xu, Shasha Yu, Wei Qu, Yuexia Chen, Liu Yang

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Article in BMC women's health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1 citing paper in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Xiaoyan Xu *Department of Pathology, The Fifth Clinical Medical College of Henan, University of Chinese Medicine (Zhengzhou People's Hospital), Zhengzhou, China.
Shasha Yu *School of Basic Medical Sciences, Nanchang Medical College, Nanchang, China.
Wei QuDepartment of Pathology, Nanchang People's Hospital, No. 1268 Jiuzhou Street, Xihu District, Nanchang, 330000, China.
Yuexia ChenDepartment of Pathology, Nanchang People's Hospital, No. 1268 Jiuzhou Street, Xihu District, Nanchang, 330000, China.
Liu YangDepartment of Pathology, Nanchang People's Hospital, No. 1268 Jiuzhou Street, Xihu District, Nanchang, 330000, China. 12805548@qq.com.

Funding

Science and Technology Program of Health Commission of Jiangxi Province 202311293
6 · The paper itself

Abstract

backgroundMammary adenoid cystic carcinoma (AdCC) is a rare subtype of invasive breast cancer. Due to its low incidence, the clinicopathological features of mammary AdCC remain incompletely understood. This study aimed to investigate the clinicopathological and molecular characteristics, therapeutic regimens, and prognostic outcomes associated with different subtypes of mammary AdCC.

methodsA total of 25 archived specimens of mammary AdCC were collected from the pathology departments of Nanchang People's Hospital and Zhengzhou People's Hospital between January 2013 and December 2024. Histomorphological evaluation, immunohistochemical (IHC) analysis, and molecular testing were performed to evaluate the clinicopathological features and prognostic outcomes. Fisher's exact test was used to analyze the relationship between HER2 status and clinicopathological features.

resultsAll 25 patients were female, with a mean age of 57.04 years. The tumors manifested as solitary solid nodules, ranging in maximum diameter from 1 to 4.5 cm. Histologically, the tumors were classified as classic adenoid cystic carcinoma (C-AdCC) (21/25), solid-basaloid AdCC (SB-AdCC) (2/25) and AdCC with high-grade transformation (2/25), with Nottingham grade II being the most common (18/25). Immunohistochemical (IHC) analysis demonstrated that most cases exhibited a triple-negative phenotype, characterized by ER-negative (21/25), PR-negative (25/25), and HER2 negativity (IHC score of 0, 1+, or 2 + with no amplification detected by FISH) (25/25). HER2-low expression (IHC score of 1+/2 + with FISH-confirmed non-amplification) was observed in 11 cases (11/25). Neuroendocrine markers were negative in all cases. MYB gene abnormalities, including break-parts or fusion, were identified in 14/25 cases. A statistically significant positive correlation (P < 0.05) was observed between HER2-low expression and MYB gene abnormalities. Axillary lymph node metastasis was observed in 2/25 patients. Following treatment, which included various surgical modalities with or without neoadjuvant chemotherapy, and a follow-up period of 6-136 months, 21 patients remained alive without recurrence or metastasis, 1 patient died at 60 months, and 3 patients were lost to follow-up.

conclusionsThese findings support the classification of mammary AdCC as a distinct triple-negative breast cancer (TNBC), with MYB gene abnormalities showing a positive correlation with HER2 status. Notably, mammary AdCC should not be indiscriminately categorized as low-grade TNBC. Precise pathological subtyping of AdCC is critical for guiding clinical management.

Indexed as

Breast NeoplasmsCarcinoma, Adenoid CysticAdultAgedClinical RelevanceErb-b2 Receptor Tyrosine KinasesFemaleHumansMiddle AgedPrognosisERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesClinicopathological featuresGene alterationsHER2-low expressionMammary adenoid cystic carcinoma(AdCC)Prognosis

Identifiers

PMID41053794
PMCPMC12502641

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