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Primary squamous cell carcinoma of major salivary gland: "Sapienza Head and Neck Unit" clinical recommendations.

Authors :
Mezi S
Pomati G
Botticelli A
De Felice F
Musio D
Della Monaca M
Amirhassankhani S
Vullo F
Cerbelli B
Carletti R
Di Gioia C
Catalano C
Valentini V
Tombolini V
Della Rocca C
Marchetti P
Source :
Rare tumors [Rare Tumors] 2020 Nov 24; Vol. 12, pp. 2036361320973526. Date of Electronic Publication: 2020 Nov 24 (Print Publication: 2020).
Publication Year :
2020

Abstract

Primary squamous cell carcinoma of salivary gland (SCG) is an extremely rare type of malignant salivary gland tumor, which in turn results in scarcity of data available regarding both its treatment and associated genetic alterations. A retrospective analysis of 12 patients with primary SCG was conducted, along with analysis of the association between treatment, clinical/pathological characteristics, and outcomes. Most patients (8) were staged IVa, with the majority of them (10) having G3 fast growing cancer. Local and systemic recurrence were reported in only three out of nine parotid cases (0 out of 2 submandibular SCGs). In two out of eight patients local relapse occurred after integrated treatment, while recurrence occurred in two out of three patients undergoing exclusive surgery. Five patients eventually died. Treatment of resectable disease must be aggressive and multimodal, with achievement of loco-regional control in order to reduce rate of recurrence and improve outcomes. Metastatic disease would require a therapeutic strategy tailored to the molecular profile in order to improve the currently disappointing results.<br />Competing Interests: Conflict of interest: The author(s) declared the following potential conflicts of interest with respect to the research, authorship, and/or publication of this article: PAOLO MARCHETTI (PM) has/had a consultant/advisory role for BMS, RocheGenentech, MSD, Novartis, Amgen, Merck Serono, Pierre Fabre, Incyte. The other authors declare they have no competing interests.<br /> (© The Author(s) 2020.)

Details

Language :
English
ISSN :
2036-3605
Volume :
12
Database :
MEDLINE
Journal :
Rare tumors
Publication Type :
Academic Journal
Accession number :
33282162
Full Text :
https://doi.org/10.1177/2036361320973526