Medicine and Oral Surgery Department, University Institute of Health Sciences (IUCS), CESPU, Gandra, Portugal.
UNIPRO, Oral Pathology and Rehabilitation Research Unit, University Institute of Health Sciences (IUCS), CESPU, Gandra, Portugal.
Oral Dis. 2024 Mar;30(2):207-215. doi: 10.1111/odi.14378. Epub 2022 Oct 22.
The aim of this study is to identify and analyze the existing literature on the utility of podoplanin to predict the risk of malignancy development (MD) in patients previously diagnosed with oral leukoplakia (OL).
A systematic review and meta-analysis (SRMA) was performed though a search strategy using several electronic databases and a combination of keywords related to podoplanin and MD of OL, until 15 May, 2022 (PROSPERO CRD42022329326). Evaluation of the risk of bias (ROB) was performed using the Quality in Prognosis Studies Tool. The meta-analyses were estimated using fixed-effect models.
From 421 articles, 6 studies were finally included, that enrolled 546 patients with OL, of whom 125 presented with an oral cancer during follow-up (32 to 90 months). Some limitations regarding the ROB were identified mostly related to small sample sizes, short follow-up times, lack of information on covariables in the included studies and lack of accuracy (including sensitivity and specificity). Meta-analysis of 6 studies reveal that high expression of podoplanin carries a pooled hazard ratio (HR) of 3.72 (95% CI, 2.40-5.76; p < 0.00001) for MD without statistical heterogeneity (I = 0%, p = 0.53).
The results of this SRMA support the role of podoplanin immunohistochemical expression as a potential predictive biomarker to assess the risk of malignancy development in oral leukoplakia.
本研究旨在识别和分析已发表的关于 Podoplanin 在预测先前诊断为口腔白斑(OL)患者发生恶性肿瘤发展(MD)风险的文献。
通过使用几个电子数据库和与 Podoplanin 和 OL 的 MD 相关的关键词组合的搜索策略进行系统评价和荟萃分析(SRMA),检索时间截至 2022 年 5 月 15 日(PROSPERO CRD42022329326)。使用预后研究质量工具(Quality in Prognosis Studies Tool)评估偏倚风险(ROB)。使用固定效应模型估计荟萃分析。
从 421 篇文章中,最终纳入了 6 项研究,共纳入了 546 名 OL 患者,其中 125 名在随访期间(32 至 90 个月)出现口腔癌。识别出一些关于 ROB 的局限性,主要涉及样本量小、随访时间短、纳入研究中缺乏协变量信息以及准确性(包括敏感性和特异性)不足。对 6 项研究的荟萃分析表明,高表达 Podoplanin 的合并危险比(HR)为 3.72(95%CI,2.40-5.76;p<0.00001),无统计学异质性(I=0%,p=0.53)。
这项 SRMA 的结果支持 Podoplanin 免疫组织化学表达作为评估口腔白斑恶性肿瘤发展风险的潜在预测生物标志物的作用。