“…We explored the National Cancer Institute's SEER 9 regulations research data (November 2017 Sub; 1973–2015; Katrina/Rita Population Adjustment) to evaluate the risks of SPM in MiSGC patients who survived for ≥6 months after diagnosis. The inclusion criteria were as follows: (1) International Classification of Diseases for Oncology, third edition (ICD‐O‐3) histologic codes for adenocarcinoma (8140, 8147, 8290, 8310, 8410, 8440, 8480, 8525, 8550, and 8491), adenoid cystic carcinoma (8200), mucoepidermoid carcinoma (8430), mixed subtype (8980), or other rare carcinomas (8012, 8041, 8082, 8500, 8562, and 8982) 14 ; (2) ICD‐O‐3 primary sites code for oral cavity (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), nasopharynx (C11.0–C11.9), 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); the anatomic sites as well as pathological categories in our including criteria were mainly based on ICD‐O‐3 topographical and histological codes that were proposed or adopted by previous studies; 4,7,15‐17 (3) tumor with malignant behavior; and (4) tumor with histologic confirmation (+) 14 . To exclude synchronous cancers, we excluded any patients in whom the second primary was detected within 6 months of diagnosis of MiSGC, followed by the criteria modified by National Cancer Institute 18 and was consistent with previous standard approaches 12,19,20 .…”