Department of Otolaryngology/Head and Neck Surgery, Amsterdam UMC, Vrije Universiteit Amsterdam, Cancer Center Amsterdam, Amsterdam, The Netherlands.
Academic Center for Dentistry Amsterdam (ACTA), Amsterdam, The Netherlands.
Int J Cancer. 2023 Jan 15;152(2):227-238. doi: 10.1002/ijc.34277. Epub 2022 Sep 18.
Oral squamous cell carcinomas (OSCCs) develop in genetically altered epithelium in the mucosal lining, also coined as fields, which are mostly not visible but occasionally present as white oral leukoplakia (OL) lesions. We developed a noninvasive genetic assay using next-generation sequencing (NGS) on brushed cells to detect the presence of genetically altered fields, including those that are not macroscopically visible. The assay demonstrated high accuracy in OL patients when brush samples were compared with biopsies as gold standard. In a cohort of Fanconi anemia patients, detection of mutations in prospectively collected oral brushes predicted oral cancer also when visible abnormalities were absent. We further provide insight in the molecular landscape of OL with frequent changes of TP53, FAT1 and NOTCH1. NGS analysis of noninvasively collected samples offers a highly accurate method to detect genetically altered fields in the oral cavity, and predicts development of OSCC in high-risk individuals. Noninvasive genetic screening can be employed to screen high-risk populations for cancer and precancer, map the extension of OL lesions beyond what is visible, map the oral cavity for precancerous changes even when visible abnormalities are absent, test accuracy of promising imaging modalities, monitor interventions and determine genetic progression as well as the natural history of the disease in the human patient.
口腔鳞状细胞癌 (OSCC) 发生于黏膜衬里的遗传改变上皮,也称为领域,这些领域大多数不可见,但偶尔表现为白色口腔白斑病 (OL) 病变。我们开发了一种使用下一代测序 (NGS) 对刷取细胞进行检测的非侵入性遗传检测方法,以检测遗传改变的领域的存在,包括那些肉眼不可见的领域。当刷取样本与活检作为金标准进行比较时,该检测方法在 OL 患者中具有很高的准确性。在范可尼贫血患者队列中,前瞻性收集的口腔刷取物中突变的检测可预测口腔癌,即使没有可见异常。我们进一步提供了 OL 的分子图谱信息,其中频繁发生 TP53、FAT1 和 NOTCH1 的突变。非侵入性采集样本的 NGS 分析提供了一种高度准确的方法来检测口腔中的遗传改变领域,并可预测高危个体发生 OSCC。非侵入性遗传筛查可用于对癌症和癌前病变高危人群进行筛查,描绘 OL 病变的延伸范围,超出肉眼可见范围,在可见异常缺失时对口腔进行癌前病变筛查,检测有前途的成像方式的准确性,监测干预措施,并确定疾病在人类患者中的遗传进展和自然史。