Deng Jiaying, Zhang Lei, Wang Zezhou, Li Bin, Xiang Jiaqing, Ma Longfei, Zhu Hongcheng, Li Yuan, Zhao Kuaile
Department of Radiation Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China.
Front Oncol. 2024 Dec 6;14:1442212. doi: 10.3389/fonc.2024.1442212. eCollection 2024.
For esophageal squamous cell carcinoma (ESCC), universally accepted pathological criteria for classification by differentiation degree are lacking. Tumor budding, single-cell invasion, and nuclear grade, recognized as prognostic factors in other carcinomas, have rarely been investigated for their correlation with differentiation and prognosis in ESCC. This study aims to determine if pathological findings can predict differentiation degree and prognosis in ESCC.
This study reviewed tumor slides from 326 patients who underwent surgery for ESCC between 2007 and 2012. Tumors were evaluated for subtypes, tumor nest size, tumor stroma, and nuclear grade (nuclear diameter and mitosis) across different differentiation groups. Overall survival (OS) and disease-free survival (DFS) were estimated using the Kaplan-Meier method, with group differences assessed using the stratified log-rank test and Cox proportional hazards model.
The mean values of tumor budding invasion margins in well, moderately, and poorly differentiated groups were 25.3%, 30.7%, and 36.3%, respectively. Mean tumor budding/10HPFs were 8.0, 10.3, and 13.0, respectively. Well-differentiated tumors showed more keratinizing subtypes, smaller tumor budding invasion margins, more Grade 1 tumor budding (0-4 cells), absence of single-cell invasion, larger nuclear diameter (≥5 lymphocytes), higher mitotic counts, more submucosal invasion, and less lymphovascular invasion. Conversely, poorly differentiated tumors exhibited opposite characteristics. Multivariate analyses identified the nuclear diameter as independent prognostic factors for OS and DFS.
Pathological features can stratify the differentiation landscape in ESCC patients. The nuclear diameter (4 lymphocytes) can help predict prognosis in ESCC than other pathological features.
We first time report the mean values of tumor budding invasion margins and tumor budding/10HPF in well, moderately, and poorly differentiated groups for esophageal squamous cell carcinoma. The landscape of well differentiation was depicted with more keratinizing subtypes, smaller tumor budding invasion margins, more Grade 1 tumor budding (0-4 cells), absence of single-cell invasion, larger nuclear diameter (≥5 lymphocytes), higher mitotic counts, and less lymphovascular invasion. The nuclear diameter as independent prognostic factors for prognosis. The findings indicate that pathological features can stratify the differentiation landscape in ESCC patients and offer novel insight into definition of well or moderately differentiation.
对于食管鳞状细胞癌(ESCC),目前缺乏被普遍接受的依据分化程度进行分类的病理标准。肿瘤芽生、单细胞浸润和核分级在其他癌症中被视为预后因素,但在ESCC中,它们与分化及预后的相关性很少被研究。本研究旨在确定病理结果能否预测ESCC的分化程度和预后。
本研究回顾了2007年至2012年间接受ESCC手术的326例患者的肿瘤切片。对不同分化组的肿瘤进行亚型、肿瘤巢大小、肿瘤基质和核分级(核直径和有丝分裂)评估。采用Kaplan-Meier法估计总生存期(OS)和无病生存期(DFS),并使用分层对数秩检验和Cox比例风险模型评估组间差异。
高分化、中分化和低分化组的肿瘤芽生浸润边缘平均值分别为25.3%、30.7%和36.3%。平均每10个高倍视野的肿瘤芽生数分别为8.0、10.3和13.0。高分化肿瘤表现出更多角化亚型、更小的肿瘤芽生浸润边缘、更多1级肿瘤芽生(0 - 4个细胞)、无单细胞浸润、更大的核直径(≥5个淋巴细胞)、更高的有丝分裂计数、更多的黏膜下浸润和更少的淋巴管浸润。相反,低分化肿瘤表现出相反的特征。多因素分析确定核直径是OS和DFS的独立预后因素。
病理特征可对ESCC患者的分化情况进行分层。与其他病理特征相比,核直径(4个淋巴细胞)有助于预测ESCC的预后。
我们首次报告了食管鳞状细胞癌高分化、中分化和低分化组的肿瘤芽生浸润边缘平均值和每10个高倍视野的肿瘤芽生数。高分化的特征表现为更多角化亚型、更小的肿瘤芽生浸润边缘、更多1级肿瘤芽生(0 - 4个细胞)、无单细胞浸润、更大的核直径(≥5个淋巴细胞)、更高的有丝分裂计数和更少的淋巴管浸润。核直径是预后的独立预后因素。研究结果表明,病理特征可对ESCC患者的分化情况进行分层,并为高分化或中分化的定义提供新的见解。