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Clinical significance of serum soluble death receptor 5 concentration in locally advanced non-small cell lung cancer patients

机译:局部晚期非小细胞肺癌患者血清可溶性死亡受体5的临床意义

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摘要

There is an urgent requirement for the identification of suitable biomarkers for the diagnosis and prognosis of non-small cell lung cancer (NSCLC). The present study aimed to measure the levels of serum soluble death receptor 5 (sDR5) in patients with locally advanced stage III NSCLC, and to evaluate its diagnostic and prognostic significance in these patients. The sDR5 concentrations were evaluated by the enzyme-linked immunosorbent assay method in 50 healthy controls and 122 patients with locally advanced stage III NSCLC [including 57 adenocarcinoma (ADC) and 65 squamous cell carcinoma (SCC) patients], before and after concurrent chemoradiotherapy. It was found that the pretreatment sDR5 levels in patients with NSCLC were higher than the sDR5 levels of healthy controls (P<0.001). However, no significant difference in the sDR5 levels was observed between the ADC and SCC subgroups (P=0.874). According to multiple clinical classifications, a significant increase in the pretreatment serum sDR5 levels could be observed in IIIB-stage patients compared with IIIA-stage patients (P=0.009). Patients with a tumor burden >3 cm had higher pretreatment sDR5 concentration than those with a tumor burden ≤3 cm (P=0.026). Additionally, T4-stage patients had significantly higher pretreatment sDR5 levels compared with those of T1-stage patients (P<0.001). There were no significant differences between pre- and post-treatment sDR5 concentrations in the total NSCLC patient group (P=0.462), ADC subgroup (P=0.066) and SCC subgroup (P=0.052). Furthermore, when patients were divided according to therapeutic response, the pretreatment sDR5 levels in the responder patients were significantly lower compared with those of the non-responders (P<0.001). Further survival analysis showed that the patients whose pretreatment sDR5 levels were ≤14 pg/ml (cutoff value, 14 pg/ml) had a longer progression-free survival (PFS) time than patients with sDR5 levels >14 pg/ml. However, no correlation was observed between the post-treatment sDR5 levels and therapeutic response or PFS time. To the best of our knowledge, the present study results provide the first evidence that the pretreatment serum levels of sDR5 may be a useful biomarker for the diagnosis, prediction and prognosis of patients with locally advanced stage III NSCLC.
机译:迫切需要鉴定合适的生物标志物以诊断和预测非小细胞肺癌(NSCLC)。本研究旨在测量局部晚期III期NSCLC患者的血清可溶性死亡受体5(sDR5)的水平,并评估其在这些患者中的诊断和预后意义。在同时放化疗前后,通过酶联免疫吸附法对50例健康对照者和122例局部晚期III期NSCLC患者(包括57例腺癌(ADC)和65例鳞状细胞癌(SCC)患者)中的sDR5浓度进行了评估。发现NSCLC患者的治疗前sDR5水平高于健康对照组的sDR5水平(P <0.001)。但是,在ADC和SCC子组之间未观察到sDR5水平的显着差异(P = 0.874)。根据多种临床分类,与IIIA期患者相比,IIIB期患者的治疗前血清sDR5水平显着增加(P = 0.009)。肿瘤负荷> 3 cm的患者比肿瘤负荷≤3cm的患者具有更高的治疗前sDR5浓度(P = 0.026)。此外,与T1期患者相比,T4期患者的治疗前sDR5水平显着更高(P <0.001)。总NSCLC患者组(P = 0.462),ADC亚组(P = 0.066)和SCC亚组(P = 0.052)的治疗前和治疗后sDR5浓度之间无显着差异。此外,根据治疗反应对患者进行分类时,与无反应者相比,有反应者的治疗前sDR5水平显着降低(P <0.001)。进一步的生存分析表明,与sDR5水平> 14 pg / ml的患者相比,治疗前sDR5水平≤14pg / ml(临界值,14 pg / ml)的患者的无进展生存时间(PFS)更长。但是,在治疗后的sDR5水平与治疗反应或PFS时间之间未发现相关性。据我们所知,本研究结果提供了第一个证据,表明血清sDR5的预处理水平可能是诊断,预测和预后局部III期非小细胞肺癌患者的有用生物标志物。

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