循环肿瘤细胞和调节t淋巴细胞在乳腺癌核心活检中的作用

S. S. Panigoro, D. Kartini, D. Wulandari, Arif Supono
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摘要

介绍。核心活检是用于乳腺癌诊断的方式之一,其灵敏度为91-99%,特异性为96-100%。这一过程会造成肿瘤组织损伤,使肿瘤细胞进入循环(CTC),引发炎症细胞的浸润。考虑到核心活检的副作用,这个过程是有争议的/矛盾的意见。在此前提下,本研究旨在探讨核心活检过程中的Tregs和CTC计数。方法。2016年8月至12月期间,一项研究招募了32名III期和IV期乳腺癌患者的血液样本,这些患者进行了核心活检。本研究采用连续抽样方法。术前、术后两周取血,流式细胞术检测Tregs (CD4、CD25、FoxP3)和CTC计数(CK19)。采用Wilcoxon检验分析CTC/Tregs计数,采用Spearman相关检验分析Tregs与CTC计数的相关性。结果。中位值为50%,p = 0.569。核心活检后Tregs计数中位数为26.31%,p = 0.049。我们发现rho值很小(r = 0.165, r = 0.235, r = 0.046), p = 0.0.5。结论:核活检前后Tregs与CTC计数无相关性。该研究表明,核心活检被认为是一种安全的乳腺癌组织病理学诊断方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Circulating Tumor Cell and Regulator T-Lymphocyte in Core Biopsy for Breast Cancer
Introduction. Core biopsy is one of the modalities used in breast cancer diagnosis, with a 91-99% sensitivity and specificity of 96-100%. The procedure causes tumor tissue damage to let tumor cells to enter circulation (CTC) and provoke the infiltration of inflammatory cells. Consider the side effect of core biopsy, the procedure to be debatable/contradicting opinions. Based on this premise, this study aims to investigate Tregs and CTC count in the core biopsy procedure. Method. A study enrolled 32 blood sample from patients of Stage III and IV breast cancer who proceed core biopsy during August to December 2016. A consecutive sampling method employed in this study. Blood specimens taken two weeks before and after the procedure, and subjected to analyze of Tregs (CD4, CD25, FoxP3) and CTC count (CK19) using flow cytometry. Wilcoxon test proceeded to analyze CTC/Tregs count and Spearman correlation test proceeded to find out the correlation of Tregsand CTC count. Results. A decrease of CTC after core biopsy found in median value of 50% in and p = 0.569. Median of Tregs count after core biopsy was 26.31%, with p = 0.049. We found a small rho values (r = 0.165, r = 0.235, r = 0.046, respectively) and p > 0.0.5. Conclusion: No correlation between Tregs with CTC count, before or after core biopsy. The study denoted that core biopsy considered a safe method for histopathological diagnostic purposes in breast cancer.
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