Bukovszky Botond, Fodor János, Tóth Erika, Kocsis Zsuzsa S, Oberna Ferenc, Ferenczi Örs, Polgár Csaba
Department of Oncology, Semmelweis University, 1122 Budapest, Hungary.
Department of Oral Diagnostics, Faculty of Dentistry, Semmelweis University, 1088 Budapest, Hungary.
J Clin Med. 2023 Jun 25;12(13):4255. doi: 10.3390/jcm12134255.
Oral or laryngeal leukoplakia has an increased risk for malignant transformation but the risk of the two anatomical sites has not been compared to each other yet.
Clinical data of 253 patients with leukoplakia (oral = 221 or laryngeal = 32) enrolled from January 1996 to January 2022 were analyzed. One hundred and seventy underwent biopsy and 83 did not. The mean follow-up time was 148.8 months. Risk factors for the malignant transformation of leukoplakia were identified using Cox proportional hazard models.
In the oral or laryngeal group, the rate of cancer was 21.7% and 50% ( = 0.002), respectively. The 10-year estimated malignant transformation was 15.1% and 42% ( < 0.0001), respectively. The laryngeal group had an increased risk of malignant transformation ( < 0.0001). The 5-year estimated survival with leukoplakia-associated cancer for the oral or laryngeal group was 40.9% and 61.1% ( = 0.337), respectively. Independent predictors of malignant transformation in the oral group were dysplasia and the grade of dysplasia of the leukoplakia, and in the laryngeal group, dysplasia had a significant impact. The malignant transformation rate was low for oral patients without biopsy or with no dysplasia, 3.9% and 5.1%, respectively. The malignant transformation occurred over 10 years.
Patients with dysplastic leukoplakia have an increased risk of malignant transformation, but the risk is higher with laryngeal than with oral leukoplakia. There is no significant difference between the groups regarding survival with leukoplakia-associated cancer. Oral patients with no dysplastic lesions have a low risk of malignant transformation. A complete excision and long-term follow up are suggested for high-risk patients to diagnose cancer in an early stage and to control late (over 10 years) malignant events.
口腔或喉白斑发生恶变的风险增加,但这两个解剖部位的风险尚未相互比较。
分析了1996年1月至2022年1月纳入的253例白斑患者(口腔白斑221例,喉白斑32例)的临床资料。170例接受了活检,83例未接受活检。平均随访时间为148.8个月。使用Cox比例风险模型确定白斑恶变的危险因素。
在口腔或喉组中,癌症发生率分别为21.7%和50%(P = 0.002)。10年估计恶变率分别为15.1%和42%(P < 0.0001)。喉组恶变风险增加(P < 0.0001)。口腔或喉组白斑相关癌症的5年估计生存率分别为40.9%和61.1%(P = 0.337)。口腔组恶变的独立预测因素是发育异常和白斑的发育异常分级,而在喉组中,发育异常有显著影响。未进行活检或无发育异常的口腔患者恶变率较低,分别为3.9%和5.1%。恶变发生在10年以上。
发育异常的白斑患者恶变风险增加,但喉白斑的风险高于口腔白斑。两组在白斑相关癌症的生存率方面无显著差异。无发育异常病变的口腔患者恶变风险较低。建议对高危患者进行完整切除并长期随访,以便早期诊断癌症并控制晚期(超过10年)恶变事件。