School of Dental Sciences, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK; Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
Evid Based Dent. 2022 Mar;23(1):36-37. doi: 10.1038/s41432-022-0240-4. Epub 2022 Mar 25.
Data sources In this systematic review and meta-analysis, Medline, Scopus and Web of Science databases were searched using Medical Subject Headings (MeSH) to identify studies assessing the risk of malignant transformation in oral lichen planus (OLP).Study selection Observational studies published in English between 2003-2020 were independently assessed for inclusion by two blinded investigators.Data extraction and synthesis Data were extracted independently by two investigators followed by discussion to reach consensus. This included: study design and patient characteristics; length of follow-up; risk of bias; method of OLP diagnosis; oral squamous cell carcinoma (OSCC) risk factors; rate of malignant transformation; and individual characteristics of malignant transformation cases. Cases of malignant transformation in the included studies were only included in meta-analysis if: 1) OLP diagnosis met current diagnostic criteria; 2) OSCC developed in the same site as previously diagnosed OLP after at least six months' follow-up; 3) the patient had no history of systemic immunosuppressive therapy, head and neck malignancy, or organ transplantation. Risk of bias was assessed using the modified Newcastle-Ottawa scale, and meta-analysis was conducted to estimate overall risk of OLP malignant transformation using the DerSimonian and Laird method. Pooled univariate odds ratios (OR) for malignant transformation were calculated based on gender, smoking status, alcohol consumption, hepatitis C infection and OLP subtype.Results In total, 593 studies were identified after removal of duplicates and 33 studies were included for data extraction. The included sample comprised 12,838 patients with OLP, and 151 malignant transformation cases were reported in the included studies. The authors excluded 56 malignant transformation cases from the meta-analysis, most commonly because of the absence of pathological OLP diagnosis. Among included malignant transformation cases, the mean (SD) age was 58.1 (12.4) years, and 64% of the sample was female. Random-effects meta-analysis estimated an OLP malignant transformation rate of 0.2% (95%CI: 0.1-0.3%). Heterogeneity was low (I2 = 28.74%, p = 0.065). Malignant transformation was significantly higher among smokers (OR = 4.62, p = 0.001), alcohol consumers (OR = 3.22, p = 0.05), those with hepatitis C (OR = 3.77, p = 0.03) and atrophic or erosive OLP subtypes (OR = 2.70, p = 0.03). Gender was not associated with increased risk of malignant transformation.Conclusions The malignant transformation rate of OLP is likely to be lower than previously reported, possibly as a result of variable diagnostic criteria. Whilst encouraging, clinical vigilance remains necessary, as OLP does carry a small risk of malignant transformation. Smoking, alcohol use, hepatitis C infection and erosive or atrophic subtypes appear to have a greater rate of malignant transformation.
在这项系统综述和荟萃分析中,我们使用医学主题词(MeSH)对 Medline、Scopus 和 Web of Science 数据库进行了检索,以确定评估口腔扁平苔藓(OLP)恶性转化风险的研究。
两位盲法评估员独立评估了 2003-2020 年期间发表的英文观察性研究,以纳入本研究。
两位评估员独立提取数据,然后进行讨论以达成共识。这包括:研究设计和患者特征;随访时间;偏倚风险;OLP 诊断方法;口腔鳞状细胞癌(OSCC)危险因素;恶性转化率;以及恶性转化病例的个体特征。如果符合以下所有标准,纳入研究中的恶性转化病例才被纳入荟萃分析:1)OLP 诊断符合当前诊断标准;2)在至少 6 个月的随访后,OSCC 在先前诊断为 OLP 的同一部位发展;3)患者无系统性免疫抑制治疗、头颈部恶性肿瘤或器官移植史。使用改良的纽卡斯尔-渥太华量表评估偏倚风险,并使用 DerSimonian 和 Laird 方法估计 OLP 恶性转化的总体风险进行荟萃分析。基于性别、吸烟状况、饮酒状况、丙型肝炎感染和 OLP 亚型,计算恶性转化的汇总单变量优势比(OR)。
去除重复项后,共确定了 593 项研究,其中 33 项研究被纳入数据提取。纳入的样本包括 12838 例 OLP 患者,在纳入的研究中报告了 151 例恶性转化病例。作者排除了荟萃分析中的 56 例恶性转化病例,最常见的原因是缺乏病理 OLP 诊断。在纳入的恶性转化病例中,平均(SD)年龄为 58.1(12.4)岁,样本中 64%为女性。随机效应荟萃分析估计 OLP 恶性转化率为 0.2%(95%CI:0.1-0.3%)。异质性较低(I2=28.74%,p=0.065)。吸烟者(OR=4.62,p=0.001)、饮酒者(OR=3.22,p=0.05)、丙型肝炎感染者(OR=3.77,p=0.03)和萎缩或糜烂性 OLP 亚型(OR=2.70,p=0.03)的恶性转化风险显著更高。性别与恶性转化风险增加无关。
OLP 的恶性转化率可能低于先前报道的水平,这可能是由于诊断标准不同。虽然令人鼓舞,但仍需保持临床警惕,因为 OLP 确实存在恶变的风险。吸烟、饮酒、丙型肝炎感染和糜烂或萎缩性亚型似乎具有更高的恶变率。