Rivera César, Gallegos Rocío, Figueroa Constanza
Department of Stomatology, Oral Medicine Group, University of Talca, North Campus, Talca, Maule Region 3460000, Chile.
School of Dentistry, Faculty of Health Sciences, University of Talca, North Campus, Talca, Maule Region 3460000, Chile.
Mol Clin Oncol. 2020 Nov;13(5):42. doi: 10.3892/mco.2020.2112. Epub 2020 Aug 13.
Identifying oral dysplastic lesions with a high risk of malignant transformation may create opportunities for early therapeutic interventions. Several tissue biomarkers have been suggested to date as prognostic indicators of the progression of dysplastic lesions to oral cancer. We herein present a systematic review (PROSPERO CRD42018086476), with the aim of identifying, evaluating and summarizing evidence on prognostic biomarkers of progression to oral cancer in patients with dysplasia. A search through MEDLINE/PubMed and Scopus databases was performed. The review only included primary articles that reported risk values associated with malignancy after a multivariate analysis. The quality of the findings was analyzed using the Reporting Recommendations for Tumor Marker Prognostic Studies, and research trends were established using SciCurve Open. A total of 4 potential biomarkers were identified: Degree of dysplasia, and the proteins retinal dehydrogenase 1, prominin-1 and podoplanin. All 3 protein biomarkers have been recognized as cancer stem cell markers. The studies were of acceptable quality, although none included sample size determinations. Due to the lack of validation and follow-up studies, these biomarkers are considered to be in a discovery phase and require validation by prospective clinical trials. The present analysis indicated that there are currently insufficient data to include these biomarkers in the clinical decision-making process.
识别具有高恶性转化风险的口腔发育异常病变可能为早期治疗干预创造机会。迄今为止,已有几种组织生物标志物被提出作为发育异常病变进展为口腔癌的预后指标。我们在此进行一项系统综述(PROSPERO CRD42018086476),目的是识别、评估和总结发育异常患者进展为口腔癌的预后生物标志物的证据。我们对MEDLINE/PubMed和Scopus数据库进行了检索。该综述仅纳入了在多变量分析后报告与恶性肿瘤相关风险值的原始文章。使用《肿瘤标志物预后研究报告建议》分析研究结果的质量,并使用SciCurve Open确定研究趋势。共识别出4种潜在生物标志物:发育异常程度,以及蛋白质视网膜脱氢酶1、prominin-1和血小板内皮细胞黏附分子。所有这3种蛋白质生物标志物均被认为是癌症干细胞标志物。这些研究质量尚可,尽管均未进行样本量测定。由于缺乏验证和随访研究,这些生物标志物被认为处于发现阶段且需要通过前瞻性临床试验进行验证。目前的分析表明,目前尚无足够数据将这些生物标志物纳入临床决策过程。