62例胃神经内分泌癌的组织学特征及预后评价

Yujie Deng, Xiaohui Chen, Yuhong Ye, Xi Shi, K. Zhu, Liming Huang, S. Zhang, Mingang Ying, Xue-de Lin
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引用次数: 7

摘要

目的探讨synaptophysin、chromogranin A、Ki-67在胃神经内分泌癌(G-NEC)中的表达及其与临床病理参数的关系,探讨可能影响预后的因素。材料与方法研究62例G-NECs的免疫组织化学特征和预后,并评估synaptophysin、chromogranin A和Ki-67的表达与临床病理变量和预后的关系。结果Chromogranin A在小细胞NECs中的表达(9/ 9,100%)高于大细胞NECs (27/ 53,51%) (p = 0.008)。Ki-67 (p = 0.494)和synaptophysin (p = 0.0.1)在NEC细胞类型间的表达均无统计学意义。相关性分析显示Ki-67的表达与胃病中三分之一(p = 0.005)和血管受累(p = 0.006)有显著相关性,与肿瘤复发有显著相关性(p = 0.078)。高表达的嗜铬粒蛋白A与小细胞NECs的组织学(p = 0.008)和较小的肿瘤最大尺寸(p = 0.038)显著相关。通过Kaplan-Meier生存估计和log-rank检验确定预后意义,结果发现早期TNM分期和术后化疗与较长的总生存期相关(p < 0.05)。单因素分析显示NECs预后不良与几个因素有关,包括TNM分期高(p = 0.048)、血管受累(p = 0.023)、复发(p = 0.004)和显微/宏观残余肿瘤(R1/2, p < 0.001)。在多变量分析中,复发被确定为唯一独立的预后因素。结论在g - nec中,存活与synaptophysin、chromogranin A或Ki-67的表达无显著相关性。我们的研究表明,早期诊断、无残留肿瘤切除和术后化疗是可能的预后因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Histological characterisation and prognostic evaluation of 62 gastric neuroendocrine carcinomas
Aim of the study To determine the significance of expression of synaptophysin, chromogranin A, and Ki-67 and their association with clinicopathological parameters, and to find out the possible prognostic factors in gastric neuroendocrine carcinoma (G-NEC). Material and methods We investigated the immunohistochemical features and prognosis of 62 G-NECs, and evaluated the association among expressions of synaptophysin, chromogranin A, and Ki-67, clinicopathological variables, and outcome. Results Chromogranin A expression was found more commonly in small-cell NECs (9/9, 100%) than in large-cell NECs (27/53, 51%) (p = 0.008). No statistical significance was found in Ki-67 (p = 0.494) or synaptophysin (p > 0.1) expression between NEC cell types. Correlation analyses revealed that Ki-67 expression was significantly associated with mid-third disease of stomach (p = 0.005) and vascular involvement (p = 0.006), and had a trend of significant correlation with tumour relapse (p = 0.078). High expression of chromogranin A was significantly associated with histology of small-cell NECs (p = 0.008) and lesser tumour greatest dimension (p = 0.038). The prognostic significance was determined by means of Kaplan-Meier survival estimates and log-rank tests, and as a result, early TNM staging and postoperative chemotherapy were found to be correlated with longer overall survival (p < 0.05). Univariate analysis revealed associations between poor prognosis in NECs and several factors, including high TNM staging (p = 0.048), vascular involvement (p = 0.023), relapse (p = 0.004), and microscopic/macroscopic residual tumour (R1/2, p < 0.001). In a multivariate analysis, relapse was identified as the sole independent prognostic factor. Conclusions No significant correlation between survival and expression of synaptophysin, chromogranin A, or Ki-67 has been determined in G-NECs. Our study indicated that early diagnosis, no-residual-tumour resection, and postoperative chemotherapy were possible prognostic factors.
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