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首页> 外文期刊>Oncoimmunology. >C-C motif chemokine 22 predicts postoperative prognosis and adjuvant chemotherapeutic benefits in patients with stage ll/lll gastric cancer
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C-C motif chemokine 22 predicts postoperative prognosis and adjuvant chemotherapeutic benefits in patients with stage ll/lll gastric cancer

机译:C-C主题趋化因子22预测术后预后和阶段LL / LLL胃癌患者的佐剂化疗益处

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摘要

Immune molecules, which have been found to be important in tumor microenvironment, seem prospective in tumor therapy, but they are still not effective enough to use in clinical practice. C-C motif chemokine 22 (CCL22) exists in various malignancies and correlates with migration of regulatory T cells, but its clinical significance in gastric cancer is still unclear. In this study, a combined data set of 466 patients with gastric cancer after surgical resection, comprised of a discovery (n = 319) and a validation data set (n = 147), was enrolled. CCL22 expression was assessed by immunohistochemical staining and we evaluated prognostic values of CCL22 staining and clinical outcomes with use of Kaplan-Meier curve and Multivariate Cox regression analysis. Positive CCL22 expression predicted adverse overall survival independent of traditional pathological grade. Multivariate analysis defined CCL22 and TNM stage as two independent prognostic factors for overall survival. Besides, in patients with TNM stage ll/lll disease, the rate of overall survival was higher among patients with CCL22-positive tumors who were treated with 5-fluorouracil based adjuvant chemotherapy than that among those who were not (P = 0.012, P < 0.001 and P < 0.001, in discovery, validation and combined data set). But for these with CCL22-negative tumors, whether to undergo adjuvant chemotherapy showed no statistical significance (P = 0.595, P = 0.085 and P = 0.252, respectively). To conclude, CCL22 was identified as an independent adverse prognostic immunobiomarker for patients with gastric cancer after surgery, which is associated with tumor-infiltrating immunocytes and could be incorporated into TNM staging system to redefine a high-risk subgroup who were more likely to benefit from 5-fluorouracil based adjuvant chemotherapy.
机译:已被发现在肿瘤微环境中具有重要的免疫分子在肿瘤疗法中似乎是前瞻性,但它们仍然不足以在临床实践中使用。 C-C基序趋化因子22(CCL22)存在于各种恶性肿瘤中,并与调节T细胞的迁移相关,但其在胃癌中的临床意义尚不清楚。在本研究中,注册了由发现(n = 319)和验证数据集(n = 147)组成的手术切除后466例胃癌患者的组合数据集。通过免疫组织化学染色评估CCL22表达,并通过使用Kaplan-Meier曲线和多变量COX回归分析评估CCL22染色和临床结果的预后值。阳性CCL22表达预测不良整体存活的完全独立于传统病理等级。多变量分析定义了CCL22和TNM阶段,作为整体存活的两个独立预后因素。此外,在患有TNM阶段LL / LL / LLL疾病的患者中,CCL22阳性肿瘤患者的整体存活率较高,患有5-氟尿嘧啶的佐剂化疗,而不是那些没有(P = 0.012,P < 0.001和p <0.001,在发现,验证和组合数据集中)。但是对于用CCL22阴性肿瘤,是否经过佐剂化疗显示没有统计学意义(P = 0.595,P = 0.085和P = 0.252)。为了得出结论,CCL22被鉴定为胃癌后胃癌患者的独立不良预后免疫标志物,其与肿瘤浸润的免疫细胞相关,并且可以掺入TNM分期系统中,以重新定义更容易受益的高风险亚组5-氟尿嘧啶基辅助化疗。

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