首页> 外文期刊>Acta biochimica Polonica >Prognostic value of broad-spectrum keratin clones AE1/AE3 and CAM5.2 in small cell lung cancer patients undergoing pulmonary resection
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Prognostic value of broad-spectrum keratin clones AE1/AE3 and CAM5.2 in small cell lung cancer patients undergoing pulmonary resection

机译:广谱角蛋白克隆AE1 / AE3和CAM5.2在小细胞肺癌肺切除患者中的预后价值

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Introduction: Small cell lung carcinoma (SCLC) is an aggressive pulmonary neoplasm of neuroendocrine origin. Keratins form a large group of intermediate filaments, which are major structural proteins in epithelial cells and carcinomas. SCLC shows a wide spectrum of keratin expression, from very strongto completely negative. A prognostic role of keratin expression in SCLC is unknown. Material and Methods: Tumor tissue microarray samples from a unique series of 82 SCLC patients who underwent pulmonary resection were stained with keratin specific antibodies AE1/AE3and CAM5.2. The percentage o1f positively stained cells and their staining pattern (diffusely membranous, partially membranous and dot-like) were evaluated. The median expression value was used for the distinction between keratin-negative and -positive patients. Overall survival in respective groups was compared using the log-rank test. Multivariate Cox proportional hazards regression analysis was performed adjusting for age, gender, tumor site, tumor stage, and tumor histology. Results: edian expression of AE1/AE3 and CAM5.2 was 80% and 90%, respectively. Five cases were completely negative for AE1/AE3 and three for Cam5.2. Median overall survival for patients with stronger and weaker AE1/AE3 staining was 24.7 and 13.8 months, respectively (p=0.019).There was no difference in survival in relation to the CAM5.2 expression (p=0.44). In multivariate analysis adjusted for CAM5.2, T and N stage, gender and age at diagnosis, stronger AE1/AE3 expression was an independent predictor of increased survival (HR 0.50; 95% CI, 0.27–0.94; p=0.031). Conclusion: High expression of AE1/AE3 is a favorable prognostic factor in surgically treated SCLC. The applicability of this finding to a typical patient population treated with non-surgical methods warrants further studies.
机译:简介:小细胞肺癌(SCLC)是神经内分泌起源的侵袭性肺肿瘤。角蛋白形成一大组中间丝,它们是上皮细胞和癌中的主要结构蛋白。 SCLC显示从非常强到完全阴性的各种角蛋白表达。角蛋白表达在SCLC中的预后作用尚不清楚。材料和方法:对82例行肺切除的SCLC患者的肿瘤组织微阵列样品进行了角蛋白特异性抗体AE1 / AE3和CAM5.2染色。评估阳性染色细胞的百分比及其染色模式(扩散膜,部分膜和点状)。中值表达值用于区分角蛋白阴性和阳性患者。使用对数秩检验比较各个组的总生存期。进行多变量Cox比例风险回归分析,调整年龄,性别,肿瘤部位,肿瘤分期和肿瘤组织学。结果:AE1 / AE3和CAM5.2的edian表达分别为80%和90%。 AE1 / AE3完全阴性5例,Cam5.2完全阴性3例。 AE1 / AE3染色较弱的患者的总生存中位数分别为24.7和13.8个月(p = 0.019)。与CAM5.2表达相关的生存期无差异(p = 0.44)。在对CAM5.2,T和N分期,性别和年龄进行诊断调整的多变量分析中,更强的AE1 / AE3表达是存活率增加的独立预测因子(HR 0.50; 95%CI,0.27-0.94; p = 0.031)。结论:AE1 / AE3的高表达是SCLC手术治疗的良好预后因素。这一发现对通过非手术方法治疗的典型患者人群的适用性值得进一步研究。

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