The value of HE4 and its combined detection on predicting recurrence and cancer death in patients with non–small cell lung cancer

医学 危险系数 内科学 比例危险模型 肿瘤科 癌胚抗原 肺癌 生物标志物 癌症 混淆 转移 接收机工作特性 生存分析 细胞角蛋白 胃肠病学 置信区间 免疫组织化学 生物 生物化学
作者
Xiaojie Zheng,Jianhong Xiao,Hui‐Ming Lin,Guohua Guo,Junhua Chen,Lijun Li,Bin Song
出处
期刊:Labmedicine [Oxford University Press]
标识
DOI:10.1093/labmed/lmaf007
摘要

Abstract Introduction Human epididymis protein 4 (HE4), a potential novel biomarker for cancers, has been widely used in clinical practice, but evidence of its prognostic value for non–small cell lung cancer (NSCLC) remain insufficient. This study aimed to explore the predictive value of serum HE4 levels on detecting recurrence or metastasis and cancer death among patients with NSCLC. Methods We included 102 cases of confirmed NSCLC and 99 healthy control individuals in our cohort study. Venous blood samples from these fasting participants were extracted upon admission for testing serum HE4 levels. Cox regression analysis was used to evaluate the risk of end point events (recurrence or metastasis and cancer death) during a 3-year follow-up. Results Among the patients with NSCLC, Kaplan-Meier analysis showed that individuals with median serum HE4 levels of 177.84 pmol/L or higher had much higher risk of recurrence or metastasis and cancer death than did individuals with median serum HE4 levels below 177.84 pmol/L (P < .005). An adjusted model by Cox regression analysis suggested strong associations between serum HE4 levels and recurrence or metastasis (hazard ratio, 2.9 [95% CI, 1.8-6.2], P < .01) and cancer death (hazard ratio, 3.8 [95% CI, 2.5-7.9], P < .01) after confounding variables, including age, sex, smoking history, drinking history and treatment methods, were adjusted for. Furthermore, receiver operating characteristic curve analysis showed that the diagnostic model combining 4 biomarkers—HE4, carcinoembryonic antigen, cytokeratin 19 fragment antigen, and squamous cell carcinoma antigen—exhibited the largest area under the curve (0.996) for diagnosing composite events, with 96.2 % sensitivity and 98.4% specificity. Discussion There was an independent correlation between high serum HE4 levels at admission and an increased risk of recurrence or metastasis and cancer death from NSCLC that supports serum HE4 as a biomarker for survival prognosis after NSCLC treatment.

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