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首页> 外文期刊>Leukemia and lymphoma >Interleukin-6 plasma levels are modulated by a polymorphism in the NF-κB1 gene and are associated with outcome following rituximab-combined chemotherapy in diffuse large B-cell non-Hodgkin lymphoma
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Interleukin-6 plasma levels are modulated by a polymorphism in the NF-κB1 gene and are associated with outcome following rituximab-combined chemotherapy in diffuse large B-cell non-Hodgkin lymphoma

机译:白细胞介素6血浆水平受NF-κB1基因多态性的调节,并与利妥昔单抗联合化疗治疗弥漫性大B细胞非霍奇金淋巴瘤的预后相关

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摘要

Peripheral blood cytokines are known prognostic parameters in diffuse large B-cell lymphoma (DLBCL) treated with chemotherapy, but their role after the introduction of rituximab is unknown. Seven polymorphisms in the promoter regions of IL-6, IL-10 and NF-κB1 genes were assessed in 167 patients with DLBCL and 99 controls and correlated with interleukin-6 (IL-6) and IL-10 plasma levels. Outcome was analyzed in 137 patients treated with rituximab-based chemotherapy. The NF-κB1 - 94ATTG deletion was associated with increased IL-6 and IL-10 in DLBCL. High IL-6 concentration correlated with unfavorable prognostic factors included in the international prognostic index (IPI) and predicted for inferior progression-free (p = 0.007) and overall survival (p = 0.02). IL-6 levels remained a significant outcome predictor also including IPI as a covariate (p = 0.006 for progression-free survival). Our data suggest that the NF-κB1 genetic background influences IL-6 production in DLBCL, and that high IL-6 concentration is an independent prognostic factor also in the "rituximab era."
机译:外周血细胞因子是用化学疗法治疗的弥漫性大B细胞淋巴瘤(DLBCL)的预后参数,但引入利妥昔单抗后其作用尚不清楚。在167例DLBCL患者和99例对照中评估了IL-6,IL-10和NF-κB1基因启动子区域的7个多态性,并与白介素6(IL-6)和IL-10血浆水平相关。结果分析了137例接受利妥昔单抗化疗的患者。 NF-κB1-94ATTG缺失与DLBCL中IL-6和IL-10升高有关。高IL-6浓度与国际预后指数(IPI)中包括的不利预后因素有关,并预测无进展的较差(p = 0.007)和总生存期(p = 0.02)。 IL-6水平仍然是重要的预后指标,也包括IPI作为协变量(无进展生存期p = 0.006)。我们的数据表明,NF-κB1的遗传背景会影响DLBCL中IL-6的产生,而且在“利妥昔单抗时代”,高浓度的IL-6是独立的预后因素。

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