Wu Wenyan, Wang Zhen, Zhou Zengtong
Resident, Department of Oral Mucosal Diseases, Shanghai Ninth People's Hospital, College of Stomatology, Shanghai Jiao Tong University School of Medicine; National Clinical Research Center for Oral Diseases; Shanghai Key Laboratory of Stomatology; and Shanghai Research Institute of Stomatology, Shanghai, People's Republic of China.
Physician, Shanghai Ninth People's Hospital, College of Stomatology, Shanghai Jiao Tong University School of Medicine; National Clinical Research Center for Oral Diseases; Shanghai Key Laboratory of Stomatology; and Shanghai Research Institute of Stomatology, Shanghai, People's Republic of China.
J Oral Maxillofac Surg. 2019 Dec;77(12):2483-2493. doi: 10.1016/j.joms.2019.08.002. Epub 2019 Aug 9.
The study aim was to investigate the risk factors for the progression of oral leukoplakia (OLK) to malignancy.
The data from 2,628 patients with OLK were retrospectively reviewed. Of these 2,628 patients, 192 had undergone sequential biopsies and were separated into 4 groups according to their final diagnosis. The risk factors were analyzed using Kaplan-Meier univariate survival analysis and Cox multivariate analysis.
In 41 of the 2,628 patients (1.7%), the OLK had progressed to cancer, with a mean interval to malignancy of 26.7 months. Of the 192 patients with sequential biopsies, OLK was maintained or had progressed to mild, moderate, or severe dysplasia or carcinoma in 50, 66, 35, and 41 patients, respectively. The 3- and 5-year oral cancer-free survival (OCFS) was 78.9 and 72.5%, respectively. The factors associated with worse overall survival were lesions located in the ventral tongue (P = .04), alcohol use (P = .025), nonhomogeneous lesions (P < .01), and high-risk dysplasia (P < .01). Cox regression analyses indicated that nonhomogeneous lesions (P = .03) and high-risk dysplasia (P < .01) were independent prognostic factors for the progression of OLK to malignancy.
High-risk dysplasia and nonhomogeneous lesions were shown to be important factors for progression to malignancy in patients with OLK. Thus, such patients should receive close follow-up and undergo sequential biopsies in the first 2 to 3 years for early screening of OLK evolving into a malignancy.
本研究旨在调查口腔白斑(OLK)恶变的危险因素。
回顾性分析2628例OLK患者的数据。在这2628例患者中,192例接受了序贯活检,并根据最终诊断分为4组。采用Kaplan-Meier单因素生存分析和Cox多因素分析对危险因素进行分析。
2628例患者中有41例(1.7%)OLK发生恶变,恶变平均间隔时间为26.7个月。在192例接受序贯活检的患者中,OLK维持原状或进展为轻度、中度或重度发育异常或癌的患者分别为50例、66例、35例和41例。3年和5年无口腔癌生存率(OCFS)分别为78.9%和72.5%。与总体生存率较差相关的因素包括位于舌腹的病变(P = 0.04)、饮酒(P = 0.025)、病变不均匀(P < 0.01)和高危发育异常(P < 0.01)。Cox回归分析表明,病变不均匀(P = 0.03)和高危发育异常(P < 0.01)是OLK恶变的独立预后因素。
高危发育异常和病变不均匀是OLK患者恶变的重要因素。因此,此类患者应密切随访,并在最初2至3年内进行序贯活检,以便早期筛查OLK是否恶变为癌症。