Journal of Oral Science Research ›› 2024, Vol. 40 ›› Issue (11): 1013-1018.DOI: 10.13701/j.cnki.kqyxyj.2024.11.013

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Clinicopathological Factors and Biomarker Immunoprofile Affecting Prognosis of Salivary Ductal Carcinoma.

BAO Luri1,2, SHI Lin1,2*   

  1. 1. Department of Pathology, Inner Mongolia Medical University, Hohhot 010010, China;
    2. Department of Pathology,Affiliated Hospital of Inner Mongolia Medical University,Hohhot 010010,China
  • Received:2024-03-06 Online:2024-11-28 Published:2024-11-27

Abstract: Objective: To explore the clinicopathological factors and biomarker immunoprofile affecting the prognosis of salivary ductal carcinoma. Methods: Retrospective analysis was applied on 23 cases of salivary ductal carcinoma including follow-up record and other clinical data collected. HE staining, immunohistochemical MaxVision two-step staining, and HER2 (HER2/Neu) gene amplification investigated by SISH were performed. Overall survival (OS) were analyzed with Kaplan-Meier curves and Cox regression. Results: Twenty-one were males and 2 were females, with an average age of 63.91 years old (39-86 years old). Tumors occurred in the parotid gland (15 cases) and submandibular gland (8 cases). Follow-up revealed 4 cases of mortality and 4 cases of relapse, while the remaining patients were survival without recurrence after surgery. The mean follow-up time was 42 months. The tumor tissue appears as heterogeneous patterns including intraductal cribriform, nest, solid, glandular tubular, and cord like structure. Acne-like necrosis was observed at the central area of the cribriform-like and solid structure. Tumor cells displayed large size, eosinophilic and granular cytoplasm, prominent and polymorphic nuclei, obvious nucleoli, dense chromatin, and visible mitotic figures. Immunophenotype was CK7 (23/23), AR (21/23), giant cystic disease liquid protein (GCDFP-15) (17/23), p53 (16/23), CK5/6 (11/23), HER2 (10/23), GATA3 (10/23), CK14 (3/23), and p63 (2/23). S-100 was not expressed. Ki-67 proliferation index ranged from 5% to 80%. CK5/6-positive cases were more often diagnosed at tumor stage Ⅲ/Ⅳ (P=0.009), while AR, HER2, GATA3, and Ki-67 proliferation indices were not related to the clinicopathological characteristics of patients (P>0.05). Univariate and multivariate survival analyses showed that clinical staging was a risk factor for OS in patients (P=0.042). Conclusion: Salivary ductal carcinoma is highly invasive, prone to recurrence and metastasis. CK5/6-positive is a potential biomarker of poor outcome in SDC.

Key words: ductal carcinoma, salivary gland tumor, clinicopathology, immunoprofile, prognosis