Department of Gastroenterology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.
Gastrointestinal Endoscopy and Medicine, Hiroshima University Hospital, Hiroshima, Japan.
Cancer Med. 2024 Feb;13(4):e7078. doi: 10.1002/cam4.7078.
Esophageal squamous cell carcinoma (ESCC) is sometimes detected in non-drinker and non-smoker females who are considered to have very low risk of ESCC development in daily practice. This study examined the clinicopathological and genomic characteristics of ESCCs in females with no history of drinking and smoking.
The sample comprised 118 ESCC lesions occurring in 95 female patients who underwent endoscopic submucosal dissection at our department between January 2008 and December 2019. The patients were categorized into two groups: 51 lesions in 49 patients with no history of drinking and smoking (nondrinker/nonsmoker [NDNS] group) and 69 lesions in 45 patients with a history of drinking or smoking (drinker/smoker [DS] group). We analyzed the differences in clinicopathological and cancerous genomic characteristics between the groups. Significant genomic alterations were validated using immunohistochemistry.
Multiple logistic regression revealed that older age, fewer multiple Lugol-voiding lesions (LVLs), and reflux esophagitis (RE) were independently associated with the occurrence of ESCCs in the NDNS group. ESCC lesions in the NDNS group were predominantly located in the mid-thoracic esophagus, posterior wall side, with 0-IIa, the aspect ratio of the lesion >2 (vertical/horizontal), and endoscopic keratinization. Genetic analysis showed that CDKN2A driver alterations were significantly more frequent and KMT2D alterations were significantly less frequent in the NDNS group than in the DS group. KMT2D alterations were strongly correlated with immunostaining.
Older nondrinker, nonsmoker females with RE and fewer multiple LVLs may develop longitudinal 0-IIa ESCC with keratinization of the posterior wall of the mid-thoracic esophagus. ESCCs in nondrinker, nonsmoker females had fewer KMT2D alterations and more CDKN2A alterations, which may be a biomarker for treatment.
在日常生活中,不饮酒且不吸烟的女性被认为发生食管鳞癌(ESCC)的风险非常低,但有时也会检测到 ESCC。本研究旨在探讨无饮酒和吸烟史的女性 ESCC 的临床病理和基因组特征。
本研究纳入了 2008 年 1 月至 2019 年 12 月在我院接受内镜黏膜下剥离术的 95 例女性患者的 118 处 ESCC 病变。患者被分为两组:无饮酒和吸烟史的 49 例患者(共 51 处病变)组成的无饮酒/不吸烟组(NDNS 组)和有饮酒或吸烟史的 45 例患者(共 69 处病变)组成的饮酒/吸烟组(DS 组)。分析了两组之间的临床病理和癌症基因组特征的差异。采用免疫组织化学验证了显著的基因组改变。
多因素逻辑回归分析显示,年龄较大、多发 Lugol 不染区(LVLs)较少和反流性食管炎(RE)与 NDNS 组 ESCC 的发生独立相关。NDNS 组的 ESCC 病变主要位于中胸段食管、后侧壁,表现为 0-IIa、病变纵横比>2(垂直/水平)和内镜下角化。基因分析显示,CDKN2A 驱动改变在 NDNS 组中显著更为常见,KMT2D 改变在 NDNS 组中显著更为少见。KMT2D 改变与免疫染色强烈相关。
RE 且 LVLs 较少的年龄较大的无饮酒、不吸烟的女性可能会发生纵向 0-IIa 型 ESCC,伴有中胸段食管后壁的角化。无饮酒、不吸烟的女性 ESCC 的 KMT2D 改变较少,CDKN2A 改变较多,这可能是治疗的生物标志物。