Longitudinal Study of Oral Precancerous Lesions: Transformation Rate and Predictive Markers for Malignancy.

IF 0.7 Q4 PHARMACOLOGY & PHARMACY
Journal of pharmacy & bioallied sciences Pub Date : 2024-07-01 Epub Date: 2024-07-31 DOI:10.4103/jpbs.jpbs_301_24
Duttatrayee Das, Anu Sumi Issac, Bhavani N Sangala, Aldrin Jerry, Ajit Jankar, Teerthesh Jain, Rohit Kumar Singh
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引用次数: 0

Abstract

Background: One of the main risk factors for the occurrence of oral cancer is oral precancerous lesions (OPLs). Early management and preventive efforts depend on knowing the transformation rate and detecting predictive signs of malignancy.

Methods: For 6 months, a group of 200 individuals with clinically diagnosed OPLs was followed up on in this longitudinal research. To examine biomarker expression levels and describe the lesions, examinations using immunohistochemistry, histopathology, and clinical methods were carried out.

Findings: Over the course of 2 years, 200 patients with OPLs were monitored in this study. Most lesions had mild dysplasia, according to histopathological examination. The expression of many biomarkers that were correlated with the dysplasia grade were p53 (60.0%), Ki-67 (40.0%), CDKN2A (30.0%), and epidermal growth factor receptor (EGFR) (25.0%).

Conclusion: In summary, this study emphasizes how crucial it is to provide patients with OPLs with individualized care plans and routine surveillance. Certain biomarkers, such EGFR, Ki-67, and p53, can be useful prognostic markers for identifying malignant transformation. To confirm these results and create tailored therapies for high-risk patients, more study is necessary.

口腔癌前病变纵向研究:恶性肿瘤的转化率和预测标志物
背景:口腔癌前病变(OPL)是口腔癌发生的主要风险因素之一。早期管理和预防工作取决于了解转化率和检测恶性肿瘤的预兆:方法:在这项纵向研究中,对 200 名临床诊断为 OPLs 的患者进行了为期 6 个月的随访。为了检测生物标志物的表达水平和描述病变,研究人员使用免疫组化、组织病理学和临床方法进行了检查:这项研究历时两年,共监测了 200 名 OPL 患者。根据组织病理学检查结果,大多数病变都有轻度发育不良。许多生物标志物的表达与发育不良等级相关,如 p53(60.0%)、Ki-67(40.0%)、CDKN2A(30.0%)和表皮生长因子受体(EGFR)(25.0%):总之,本研究强调了为 OPL 患者提供个体化护理计划和常规监测的重要性。某些生物标志物,如表皮生长因子受体(EGFR)、Ki-67 和 p53,可作为识别恶性转化的有用预后标志物。要证实这些结果并为高危患者量身定制治疗方案,还需要进行更多的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
1.40
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