“…Patients were included in our study if the following criteria were met: 1) histologic subtypes identified using the third-edition ICD for Oncology (ICD-O3) codes for adenocarcinoma (8140, 8147, 8290, 8310, 8410, 8440, 8480, 8525, and 8550), mucoepidermoid carcinoma (8430), adenoid cystic carcinoma (8200), mixed subtype (8980 and 8981), and other rare carcinomas (8012, 8041, 8082, 8562, and 8982), which was the same as the methodology of previous studies using the SEER database; 3 , 9 , 21 2) histologic subtypes confirmed by aspiration cytology, biopsy, or postoperative pathology report; 3) primary site included oral cavity (ICD-O3 topography codes C00.0–C00.9, C02.0–C02.3, C02.8–C02.9, C03.0–C03.9, C04.0–C04.9, C05.0, and C06.0–C06.1), oropharynx (C01.9, C02.4, C05.1–C05.2, and C09.0–C10.9), larynx (C32.0–C32.9), hypopharynx (C12.9–C13.2), nasal cavity (C30.0), and paranasal sinus (C31.0–C31.9). MiSGCs originating from nasopharynx (C11.0–C11.9) were excluded, as none of these patients had undergone PTS, and more importantly almost all these tumors were recorded as lymphoepithelial carcinoma (8082), which was difficult to distinguish from the more common primary nasopharyngeal SCC; 2 4) patients diagnosed between January 1, 2004 and June 30, 2014, because some important factors are merely available for patients diagnosed after 2004, such as the American Joint Committee on Cancer (AJCC) TNM staging.…”