Huang Z, Xu D, Zhang F, Ying Y, Song L
Department of Internal Medicine Oncology, Shandong Cancer Hospital and Institute, No. 440 Jiyan Road, Jinan, 250117, China.
Shandong Academy of Medical Sciences, School of Medicine and Life Sciences, University of Jinan, Jinan, China.
Clin Transl Oncol. 2016 Oct;18(10):1019-25. doi: 10.1007/s12094-015-1479-4. Epub 2016 Feb 17.
The aim of this study was (1) to evaluate and predict the value of ProGRP and NSE in therapy and survival; (2) as well as to investigate the correlation between the ProGRP mRNA expression in peripheral blood and serum ProGRP protein.
The study included 122 patients with SCLC without prior therapy. The serum levels of ProGRP and NSE were detected by enzyme-linked immunosorbent assay and eletro-chemiluminescence immunoassay, respectively. The expression of ProGRP mRNA was detected by real-time reverse transcriptase-polymerase chain reaction.
Distribution of serum levels of ProGRP, NSE and ProGRP mRNA differed significantly according to tumor size, disease stage and distant metastasis (all P < 0.05), and no association was found between them and gender or age (both P > 0.05). After two courses of chemotherapy, patients of remission and stable groups showed a marked decrease in ProGRP and NSE concentrations (P < 0.05). The ProGRP concentration of patients in progression group was significantly higher than pretreatment level (P < 0.05), while NSE concentration was not. A linear nonparametric (Spearman) correlation test revealed that there was a significant correlation between ProGRP mRNA expression in peripheral blood and serum ProGRP protein level (P < 0.05). Univariate analysis found a statistically significant association of survival with disease stage, distant metastasis, ProGRP and NSE (P < 0.05). Gender, age and tumor size were not prognostic factors (P > 0.05). Multiple Cox regression model analysis found that only disease stage and NSE were significant predictors (P < 0.05).
This study has found that there is a potential role for ProGRP and NSE in both therapy monitoring and predicting survival in SCLC patients.
本研究的目的是(1)评估和预测ProGRP和NSE在治疗及生存方面的价值;(2)并研究外周血中ProGRP mRNA表达与血清ProGRP蛋白之间的相关性。
本研究纳入122例未经前期治疗的小细胞肺癌患者。分别采用酶联免疫吸附测定法和电化学发光免疫测定法检测血清ProGRP和NSE水平。采用实时逆转录-聚合酶链反应检测ProGRP mRNA的表达。
血清ProGRP、NSE水平及ProGRP mRNA表达根据肿瘤大小、疾病分期和远处转移的不同有显著差异(均P<0.05),且未发现它们与性别或年龄之间存在关联(均P>0.05)。经过两个疗程的化疗后,缓解组和稳定组患者的ProGRP和NSE浓度显著降低(P<0.05)。进展组患者的ProGRP浓度显著高于治疗前水平(P<0.05),而NSE浓度则无变化。线性非参数(Spearman)相关性检验显示,外周血中ProGRP mRNA表达与血清ProGRP蛋白水平之间存在显著相关性(P<0.05)。单因素分析发现,生存与疾病分期、远处转移、ProGRP和NSE之间存在统计学显著关联(P<0.05)。性别、年龄和肿瘤大小不是预后因素(P>0.05)。多因素Cox回归模型分析发现,只有疾病分期和NSE是显著的预测因素(P<0.05)。
本研究发现,ProGRP和NSE在小细胞肺癌患者的治疗监测和生存预测方面均具有潜在作用。