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首页> 外文期刊>Journal of Cancer >CD68- and CD163-positive tumor infiltrating macrophages in non-metastatic breast cancer: a retrospective study and meta-analysis
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CD68- and CD163-positive tumor infiltrating macrophages in non-metastatic breast cancer: a retrospective study and meta-analysis

机译:非转移性乳腺癌中CD68和CD163阳性的肿瘤浸润巨噬细胞:回顾性研究和荟萃分析

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Studies have indicated the significance of tumor associated macrophages (TAMs) in breast cancer; however, inconsistent results still exist. We retrospectively reviewed the macrophage distribution in 1579 breast cancer specimens with anti-CD68 or anti-CD163 immunohistochemical staining, and further analyzed the overall survival data. Furthermore, we performed a retrospective study and systematic review of the published studies on CD68- and CD163-positive macrophages in non-metastatic breast cancer. 13 studies with 5116 patients were included in this meta-analysis. Our own data revealed a high density of both CD68- and CD163-positive TAMs that was significantly related to lymph node metastasis (CD68, P = 0.003; CD163, P 0.001); high Ki67 (CD68, P = 0.026; CD163, P 0.001), poor histological grade (CD68, P 0.001; CD163, P 0.001) and hormonal receptor negativity (CD68, P 0.001; CD163, P 0.001); only CD163-positive TAMs were associated with poor overall survival ( P = 0.003). Nonetheless, the meta-analysis only found that CD68- and CD163-positive TAMs were associated with high Ki67 [CD68, Relative risk (RR): 1.18, 95% confidence interval (CI): 1.09-1.28; CD163, RR: 1.75, 95% CI: 1.39-2.20], advanced histological grade (CD68, RR: 1.72, 95% CI: 1.46-2.03; CD163, RR: 1.99, 95% CI: 1.35-2.94) and low hormonal receptor levels (CD68, RR: 0.75, 95% CI: 0.69-0.82; CD163, RR: 0.82, 95% CI: 0.74-0.90), but not lymph node metastasis and HER2 expression. This meta-analysis further supports the clinical significance of TAMs in breast cancer, and both CD68- and CD163-positive TAMs could be prognostic markers in non-metastatic breast cancer.
机译:研究表明肿瘤相关巨噬细胞(TAM)在乳腺癌中的重要性。但是,结果仍然存在不一致。我们回顾性回顾了1579例乳腺癌组织中巨噬细胞的抗CD68或抗CD163免疫组织化学染色,并进一步分析了整体生存数据。此外,我们对非转移性乳腺癌中CD68和CD163阳性巨噬细胞的已发表研究进行了回顾性研究和系统评价。这项荟萃分析包括13项针对5116例患者的研究。我们自己的数据显示,CD68和CD163阳性TAM的高密度与淋巴结转移显着相关(CD68,P = 0.003; CD163,P <0.001); Ki67高(CD68,P = 0.026; CD163,P <0.001),组织学评分差(CD68,P <0.001; CD163,P <0.001)和激素受体阴性(CD68,P <0.001; CD163,P <0.001);只有CD163阳性的TAM与总生存期差有关(P = 0.003)。然而,荟萃分析仅发现CD68和CD163阳性TAM与高Ki67相关[CD68,相对风险(RR):1.18,95%置信区间(CI):1.09-1.28; CD163,RR:1.75,95%CI:1.39-2.20],高级组织学分级(CD68,RR:1.72,95%CI:1.46-2.03; CD163,RR:1.99,95%CI:1.35-2.94)和低激素受体水平(CD68,RR:0.75,95%CI:0.69-0.82; CD163,RR:0.82,95%CI:0.74-0.90),但不包括淋巴结转移和HER2表达。这项荟萃分析进一步支持了TAM在乳腺癌中的临床意义,并且CD68和CD163阳性TAM均可作为非转移性乳腺癌的预后标志物。

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