Primary neuroendocrine breast carcinomas: a retrospective analysis and review of literature
- PMID: 28176908
- PMCID: PMC5261841
- DOI: 10.2147/OTT.S113736
Primary neuroendocrine breast carcinomas: a retrospective analysis and review of literature
Erratum in
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Erratum: Primary neuroendocrine breast carcinomas: a retrospective analysis and review of literature [Corrigendum].Onco Targets Ther. 2017 Mar 21;10:1707. doi: 10.2147/OTT.S135552. eCollection 2017. Onco Targets Ther. 2017. PMID: 28356757 Free PMC article.
Abstract
Background: Primary neuroendocrine breast carcinomas (NEBCs) are a rare type of breast carcinomas that lack comprehensive recognition, including the clinicopathological features, therapeutic strategies, and prognostic significance. The aim of this retrospective analysis is to present and analyze our own data of primary NEBCs.
Materials and methods: We retrospectively reviewed the medical records from 2005 to 2015 in The First Affiliated Hospital of Chongqing Medical University, Chongqing, People's Republic of China to obtain a cohort of breast carcinoma patients who were confirmed to have primary NEBC by histopathology. The detailed clinical data along with histopathology, treatment, and follow-up aspects were gathered for analysis.
Results: This retrospective analysis included 19 patients with a histopathological diagnosis of primary NEBC from 2005 to 2015. Their mean age was 59.2 years (ranging from 17 to 82 years). The majority of patients (15/19) focused on stages I and II. Of the 15 patients, 14 were positive for estrogen receptor, and 11 were positive for progesterone receptor. For neuroendocrine markers, the expression rates were 8/19, 14/18, 12/14, and 2/6 for chromogranin A, synaptophysin, neuron-specific enolase, and CD56, respectively. All operable patients except the one stage M1 underwent a surgery and 4/18 had axillary lymph node metastasis. Chemotherapy was performed in 12/19, and endocrine therapy in 8/10. With a median follow-up of 59.2 months, only 2 cases progressed after postoperative systemic therapy.
Conclusion: The understanding of NEBC is limited due to its rarity. More evidence should be provided to enhance the understanding of NEBC, especially for diagnosis, treatment, and prognosis.
Keywords: diagnosis; follow-up; primary neuroendocrine breast carcinomas; therapy.
Conflict of interest statement
The authors report no conflicts of interest in this work.
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