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早期口腔舌癌中的新兴组织病理学标志物:系统评价和荟萃分析。

Emerging histopathologic markers in early-stage oral tongue cancer: A systematic review and meta-analysis.

机构信息

Cancer and Translational Medicine Research Unit, Medical Research Center Oulu, University of Oulu and Oulu University Hospital, Oulu, Finland.

Department of Oral and Maxillofacial Diseases, University of Helsinki, Helsinki, Finland.

出版信息

Head Neck. 2022 Jun;44(6):1481-1491. doi: 10.1002/hed.27022. Epub 2022 Feb 28.

Abstract

Although there are many histopathologic prognosticators, grading of early oral tongue squamous cell carcinoma (OTSCC) is still based on morphological cell differentiation which has low prognostic value. Here we summarize the emerging histopathological markers showing powerful prognostic value, but are not included in pathology reports. Using PubMed, Scopus, Ovid Medline, and Web of Science databases, a systematic literature search was preformed to identify early OTSCC studies that investigated the prognostic significance of hematoxylin-eosin-based histopathologic markers. Our meta-analysis showed that tumor budding was associated with overall survival (hazard ratio [HR] 2.32; 95% CI 1.40-3.84; p < 0.01) and disease-specific survival (DSS) (1.89; 95% CI 1.13-3.15; p = 0.02). Worst pattern of invasion was associated with disease-free survival (DFS) (1.95; 95% CI 1.04-3.64; p = 0.04). Tumor-stroma ratio was also associated with DFS (1.75, 95% CI 1.24-2.48; p < 0.01) and DSS (1.69; 95% CI 1.19-2.42; p < 0.01). Tumor budding, worst pattern of invasion, and tumor-stroma ratio have a promising prognostic value in early OTSCC. The evaluation and reporting of these markers is cost-effective and can be incorporated in daily practice.

摘要

尽管有许多组织病理学预后标志物,但早期口腔舌鳞状细胞癌(OTSCC)的分级仍然基于形态学细胞分化,其预后价值较低。在这里,我们总结了新兴的组织病理学标志物,这些标志物具有强大的预后价值,但不包括在病理报告中。使用 PubMed、Scopus、Ovid Medline 和 Web of Science 数据库,进行了系统的文献检索,以确定研究早期 OTSCC 中基于苏木精-伊红的组织病理学标志物预后意义的研究。我们的荟萃分析表明,肿瘤芽与总生存率(危险比 [HR] 2.32;95%置信区间 1.40-3.84;p<0.01)和疾病特异性生存率(DSS)(1.89;95%置信区间 1.13-3.15;p=0.02)相关。侵袭最严重的模式与无病生存率(DFS)(1.95;95%置信区间 1.04-3.64;p=0.04)相关。肿瘤-基质比也与 DFS(1.75,95%置信区间 1.24-2.48;p<0.01)和 DSS(1.69;95%置信区间 1.19-2.42;p<0.01)相关。肿瘤芽、侵袭最严重的模式和肿瘤-基质比在早期 OTSCC 中具有有前途的预后价值。这些标志物的评估和报告具有成本效益,可以纳入日常实践。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bc9/9545479/1d04510d9293/HED-44-1481-g003.jpg

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