Oral Diagnosis Department, Piracicaba Dental School, University of Campinas (UNICAMP), Av. Limeira, 901, Piracicaba, São Paulo, 13414-903, Brazil.
Private Pathology Service, Getúlio Sales Diagnósticos, GSD, Natal, Rio Grande Do Norte, Brazil.
Head Neck Pathol. 2024 Nov 30;18(1):127. doi: 10.1007/s12105-024-01732-4.
This study aimed to conduct a systematic review summarizing the clinicopathological, prognostic, and molecular features of salivary gland intraductal carcinoma (SGIC).
This study followed the PRISMA 2020 guidelines and was registered in the PROSPERO database. It included case reports, case series studies, and cohort studies of SGIC indexed in the PubMed, Web of Science, Scopus, and Embase databases published between 1983 and 2024. Collected variables underwent descriptive analysis, association analysis using Fisher's tests, and Kaplan-Meier analysis. The quality assessment of the included studies was conducted using the Joanna Briggs Institute tools.
This systematic review yielded 59 studies, comprising 186 SGIC cases. Most of cases involved the parotid gland of male patients around 60 years old. Lesions predominantly exhibited noninvasive growth, an intercalated duct phenotype, and minimal pleomorphism. Most of the patients did not develop recurrent or metastatic disease, indicating a good prognosis. However, male sex, invasive lesions, adjuvant treatments, high-grade lesions, as well as lymph node or distant metastasis negatively affected the survival rates. Overall SGIC cases showed S100, mammaglobin, SOX10, AR, CK7, p63, calponin, CK14, SMA, and p40 positivity and a low Ki67 index. Common molecular alterations included NCOA4-RET, TRIM33-RET, and TRIM27-RET fusions, and HRAS, PIK3CA, and BRAF V600E mutations.
SGIC is a histopathologically and molecularly heterogeneous lesion with an overall excellent prognosis. The presence of invasive lesions, as well as lymph node or distant metastasis, has emerged as one of the most critical prognostic factors in SGIC patients.
本研究旨在进行系统综述,总结唾液腺导管内癌(SGIC)的临床病理、预后和分子特征。
本研究遵循 PRISMA 2020 指南,并在 PROSPERO 数据库中进行了注册。纳入了 1983 年至 2024 年在 PubMed、Web of Science、Scopus 和 Embase 数据库中索引的 SGIC 病例报告、病例系列研究和队列研究。收集的变量进行了描述性分析、Fisher 检验的关联分析和 Kaplan-Meier 分析。使用 Joanna Briggs 研究所工具对纳入研究进行质量评估。
本系统综述共纳入 59 项研究,包含 186 例 SGIC 病例。大多数病例涉及男性患者的腮腺,年龄在 60 岁左右。病变主要表现为非浸润性生长、中间导管表型和最小的多形性。大多数患者未出现复发或转移疾病,提示预后良好。然而,男性、浸润性病变、辅助治疗、高级别病变以及淋巴结或远处转移均对生存率产生负面影响。总体而言,SGIC 病例表现出 S100、乳球蛋白、SOX10、AR、CK7、p63、钙调蛋白、CK14、SMA 和 p40 阳性以及 Ki67 指数较低。常见的分子改变包括 NCOA4-RET、TRIM33-RET 和 TRIM27-RET 融合,以及 HRAS、PIK3CA 和 BRAF V600E 突变。
SGIC 是一种组织病理学和分子学上具有异质性的病变,总体预后良好。浸润性病变的存在,以及淋巴结或远处转移,已成为 SGIC 患者最重要的预后因素之一。