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首页> 外文期刊>Scandinavian journal of clinical and laboratory investigation. >Macrophage activation marker soluble CD163 may predict disease progression in hepatocellular carcinoma
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Macrophage activation marker soluble CD163 may predict disease progression in hepatocellular carcinoma

机译:巨噬细胞活化标记物可溶性CD163可能预测肝细胞癌的疾病进展

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摘要

Background: Tumor associated macrophages are present in hepatocellular carcinoma (HCC) and associated with a poor prognosis. The aim of the present study was to investigate the levels and dynamics of soluble (s)CD163, a specific macrophage activation marker, in patients with HCC. Methods: In a cohort from Australia, we studied 109 HCC patients, 116 patients with chronic liver disease (CLD), and 52 healthy controls. We examined associations between baseline sCD163 and parameters of HCC severity as well as overall and progression-free survival. In a cohort of 42 Danish HCC patients, we measured sCD163 at baseline and 1, 4 and 12 weeks after ablative treatment. Results: In the Australian cohort, median sCD163 was similarly increased in HCC (5.6[interquartile range 3.5-8.0] mg/L) and CLD (6.1[3.6-9.6] mg/L) patients as compared to controls (2.0[1.5-2.7] mg/L, p<0.001). sCD163 correlated with Child-Pugh and MELD scores in both HCC and CLD patients. Patients with high sCD163 levels had shorter progression-free survival (p<0.001), but not overall survival (p=0.15). In the Danish cohort, patients with HCC progression at 12 weeks had an increase in sCD163. There was no association between sCD163 and HCC size, number, vascular invasion or metastasis in any of the cohorts. Conclusions: We confirmed increased sCD163 levels in CLD and HCC patients associated with Child-Pugh and MELD scores and portal hypertension, but not with HCC size and number, or metastasis. As a novel finding, baseline sCD163 appeared to predict a rapid HCC progression, as sCD163 increased during follow-up in HCC patients who showed progression.
机译:背景:肿瘤相关的巨噬细胞存在于肝细胞癌(HCC)中,且预后不良。本研究的目的是研究HCC患者可溶性巨噬细胞活化标记物CD163的水平和动力学。方法:在来自澳大利亚的队列中,我们研究了109例HCC患者,116例慢性肝病(CLD)患者和52例健康对照者。我们检查了基线sCD163和HCC严重性参数以及总体生存和无进展生存之间的关联。在一组42名丹麦HCC患者中,我们在基线以及消融治疗后1、4和12周测量了sCD163。结果:在澳大利亚队列中,与对照组(2.0 [1.5-1.5 2.7] mg / L,p <0.001)。 sCD163与HCC和CLD患者的Child-Pugh和MELD得分相关。 sCD163水平高的患者的无进展生存期较短(p <0.001),但总生存期则没有(p = 0.15)。在丹麦队列中,HCC进展为12周的患者的sCD163增加。 sCD163与HCC大小,数量,任何血管侵入或转移之间均无关联。结论:我们证实CLD和HCC患者的sCD163水平升高与Child-Pugh和MELD评分以及门脉高压相关,但与HCC的大小,数量或转移无关。作为一项新发现,基线sCD163似乎可预测HCC的快速进展,因为在随访中显示进展的HCC患者在随访期间sCD163升高。

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