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Albumin‐to‐fibrinogen ratio as a promising biomarker to predict clinical outcome of non‐small cell lung cancer individuals

机译:白蛋白与纤维蛋白原比率可预测非小细胞肺癌患者的临床结局

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摘要

Chronic inflammation is one of the critical causes to promote the initiation and metastasis of solid malignancies including lung cancer (LC). Here, we aimed to investigate the prognostic roles of albumin (Alb)‐to‐fibrinogen (Fib) ratio (AFR), Fib and Alb in LC and to establish a novel effective nomogram combined with AFR. Four hundred twelve LC patients diagnosed between February 2005 and December 2014 were recruited in this prospective study. The prognostic roles of AFR, Fib, Alb, neutrophil‐to‐lymphocyte ratio (NLR), platelet‐to‐lymphocyte ratio (PLR) and monocyte‐to‐lymphocyte ratio (MLR) were identified by X‐tile software, Kaplan–Meier curve, Cox regression model, and time‐dependent ROC. Pretreatment high circulating Fib, low AFR, and Alb were significantly associated with increased risk of death for LC patients, especially for non‐small cell lung cancer (NSCLC) patients in all stages. The area under curves (AUCs) of AFR, Fib, and NLR were higher than them within Alb and style="fixed-case">PLR for predicting the survival of style="fixed-case">NSCLC patients. Moreover, we found that clinical outcome of high style="fixed-case">AFR patient with chemo‐radiotherapy was superior to low style="fixed-case">AFR patient; overall survival rate of stage style="fixed-case">II‐ style="fixed-case">III NSCLC patients undergoing chemo‐radiotherapy was significantly lower than the surgical patients with treatment of adjuvant chemo‐radiotherapy(P = 0.001) in low style="fixed-case">AFR subgroup. On the contrary, clinical outcome of the patients receiving chemo‐radiotherapy was the same to the patients undergoing surgery and adjuvant chemo‐radiotherapy (P = 0.405) in high style="fixed-case">AFR subgroup. In addition, c‐index of predicted nomogram including style="fixed-case">AFR (0.717) for style="fixed-case">NSCLC patients with treatment of chemo‐radiotherapy was higher than that without style="fixed-case">AFR (0.707). Our findings demonstrated that circulating pretreatment style="fixed-case">AFR might be a potential biomarker to predict clinical efficacy of surgical resection and adjuvant chemo‐radiotherapy and be a prognostic biomarker for style="fixed-case">NSCLC individuals.
机译:慢性炎症是促进包括肺癌(LC)在内的实体恶性肿瘤发生和转移的关键原因之一。在这里,我们旨在调查白蛋白(Alb)-纤维蛋白原(Fib)比(AFR),Fib和Alb在LC中的预后作用,并建立与AFR结合的新型有效诺模图。在这项前瞻性研究中,招募了2005年2月至2014年12月之间的412名LC患者。通过X-tile软件Kaplan-Meier确定了AFR,Fib,Alb,中性白细胞与淋巴细胞之比(NLR),血小板与淋巴细胞之比(PLR)和单核细胞与淋巴细胞之比(MLR)的预后作用曲线,Cox回归模型和时间相关的ROC。预处理高循环Fib,低AFR和Alb与LC患者尤其是所有阶段的非小细胞肺癌(NSCLC)患者的死亡风险增加显着相关。 AFR,Fib和NLR的曲线下面积(AUC)高于Alb和 style =“ fixed-case”> PLR 中的区域,以预测 style =“ fixed-case”的生存时间> NSCLC 患者。此外,我们发现高 style =“ fixed-case”> AFR 患者接受化学放射治疗的临床结果优于低 span style =“ fixed-case”> AFR 患者。 style =“ fixed-case”> II - span style =“ fixed-case”> III NSCLC 阶段接受化学放射治疗的患者的总生存率显着低于接受手术放疗的患者低 style =“ fixed-case”> AFR 亚组的辅助化疗放疗(P = 0.001)。相反,在高 style =“ fixed-case”> AFR 亚组中,接受化学放射治疗的患者的临床结局与接受手术和辅助化学放射治疗的患者(P = 0.405)相同。此外, style =“ fixed-case”> NSCLC 接受化学疗法治疗的患者的预测列线图的c-index包括 style =“ fixed-case”> AFR (0.717)放射疗法比没有 style =“ fixed-case”> AFR 的放射疗法要高(0.707)。我们的研究结果表明,循环预处理 style =“ fixed-case”> AFR 可能是预测手术切除和辅助化学放疗的临床疗效的潜在生物标志物,并且是 style =“ fixed”的预后生物标志物-case“> NSCLC 个人。

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