Abstract

PurposeThe aim of the study was to assess the treatment results of the parotid gland salivary duct carcinoma (SDC).Material and methodsA retrospective clinicopathological analysis of 40 patients treated for parotid SDC in 1996–2015 was performed. The impact of following factors on 5-year disease-free survival (DFS) and overall survival (OS) was studied: age, sex, preoperative 7th nerve palsy, skin infiltration, pT, pN, surgical margin, type of parotidectomy and neck dissection, histology (SDC de novo vs. SDC ex pleomorphic adenoma, SDCexPA), intra/periparotid lymph nodes metastases, perineural invasion (PNI), extraparenchymal extension (EPE), and overexpression HER2.ResultsThe average age of the patients was 62 years (ranged from 39 to 81). Males predominated (57.5%). Patients with the clinical stage IV predominated (82.5%). In 1/3 of patients preoperative, 7th nerve palsy occurred. All patients were treated surgically, and all but one had supplementary radiotherapy. In 28 patients (70%), total radical parotidectomy was performed. A neck dissection was performed in all patients. In 19 cases (47.5%), SDCexPA was diagnosed. Negative microscopic surgical margin was obtained in 60% of patients. The follow-up for the whole analyzed group ranged from 2 to 22 years, average was 11.6 years. In 23 patients (57.5%), the disease recurred. Local recurrence was observed in 10 (25%) and distant metastases in 15 (37.5%) cases. 20 patients (50%) died of cancer. 5-year DSF and OS were 42.5% and 41%, respectively. Univariate analysis proved that the significant influence on the survival had 7th nerve palsy (p = 0.024 and p = 0.017, respectively), higher pT-stage (p < 0.001), radical parotidectomy (p = 0.024 and p = 0.022), radical treatment of the neck (p = 0.001 and p = 0.002), EPE (p = 0.040 and p = 0.028), and histology SDCexPA and PNI (p = 0.036 and 0.048). Multivariate analysis showed that independent prognostic factors were the 7th nerve palsy and the histology SDCexPA, which worsened 5-year DFS, respectively, 3.61 and 3.94 times (p = 0.033 and p = 0.026). On the other hand, on 5-year OS, only 7th nerve palsy had an influence (3.86 times worse prognosis, p = 0.033).ConclusionsSDC is a clinically aggressive cancer with high risk of local recurrence and distant metastases, however, with a chance of curing of around 40%. In the majority of patients, a radical surgical treatment is necessary due to the high clinical stage of disease. Worse prognosis have patients with preoperative 7th nerve palsy and in whom SDC develops in pleomorphic adenoma.

Highlights

  • Salivary duct carcinoma (SDC) was described by Kleinsasser in 1968 [1]

  • In 1996–2015, 159 patients with primary parotid gland carcinoma were treated in the Department of Otolaryngology, of which 40 (25.1%) were diagnosed with salivary duct carcinoma

  • Histological diagnosis was confirmed according to the WHO classification of salivary gland tumors from 2017 [3]

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Summary

Introduction

Salivary duct carcinoma (SDC) was described by Kleinsasser in 1968 [1]. SDC may develop de novo or within the pleomorphic adenoma (salivary duct carcinoma ex pleomorphic adenoma, SDCexPA) [3]. SDC represents < 1.8% of all major salivary gland tumors and about 10% of all salivary gland malignancies [4]. It is, a relatively rare cancer; its occurrence may be underestimated in patients with tumors classified as carcinoma. Clinical series from single centers showing SDC count from several to several dozen patients are an important source of information about this cancer, as each case report provides new or confirms known information about its clinical course and prognosis. Due to differences in symptomatology and treatment between individual major salivary glands, the authors decided to present their own SDC located only in the parotid gland

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