Wieskopf B, Demangeat C, Purohit A, Stenger R, Gries P, Kreisman H, Quoix E
Hopitaux Universitaries de Strasbourg, France.
Chest. 1995 Jul;108(1):163-9. doi: 10.1378/chest.108.1.163.
Cytokeratins are epithelial markers whose expression is not lost during malignant transformation. Cyfra 21-1 is a cytokeratin-19 fragment that is soluble in serum and may be a useful circulating tumor marker.
The aims of this study were (1) to confirm sensitivity and specificity of Cyfra 21-1 in detecting non-small cell lung cancer (NSCLC) and especially the squamous cell subtype, (2) to assess the potential relationship between Cyfra 21-1 and disease stage of the disease in NSCLC, and (3) to evaluate prognostic effect of Cyfra 21-1 in NSCLC.
An immunoradiometric assay of serum Cyfra 21-1 was performed in 161 patients with lung cancers and 71 others with benign lung diseases. The ability of Cyfra 21-1 to detect different histologic subtypes of lung cancer vs benign lung diseases was assessed through receiver operating characteristic (ROC) curves and comparisons with other tumor markers such as carcinoembryonic antigen, neuron-specific enolase, and squamous cell carcinoma antigen. Comparisons of Cyfra 21-1 levels according to histologic subtype and disease stage were done using Kruskal-Wallis test. Independent prognostic value of Cyfra 21-1 was studied with a multivariate analysis of survival (Cox's model).
Using a threshold of 3.3 ng/mL for Cyfra 21-1, sensitivity and specificity were, respectively, 0.59 and 0.94 in NSCLC, 0.68 and 0.94 in the subgroup of the squamous cell carcinoma, and 0.19 and 0.94 in small cell lung cancer. Cyfra 21-1 levels were significantly higher in advanced NSCLC than in early-stage disease. All 29 patients with serum concentrations > 32 ng/mL had stage IIIB-IV and only one of 14 patients with stage I-II disease had Cyfra 21-1 level > 18 ng/mL. In the multivariate analysis of survival, Cyfra 21-1 was an independent prognostic factor along with performance status and disease stage in NSCLC.
Cyfra 21-1 is a sensitive and specific tumor marker of NSCLC, especially of squamous cell subtype. It also reflects the extent of the disease and has an independent prognostic role along with performance status and disease stage in NSCLC.
A high level of Cyfra 21-1 in apparently early-stage NSCLC should be an indication for more extensive workup before thoracotomy. The independent prognostic role of Cyfra 21-1 level may be useful in stratifying populations with advanced NSCLC or early-stage resected NSCLC as elevated Cyfra 21-1 levels might identify those patients at high risk for treatment failure.
细胞角蛋白是上皮标志物,其表达在恶性转化过程中不会丧失。细胞角蛋白19片段(Cyfra 21-1)是一种可溶于血清的细胞角蛋白,可能是一种有用的循环肿瘤标志物。
本研究的目的是(1)确认Cyfra 21-1在检测非小细胞肺癌(NSCLC)尤其是鳞状细胞亚型中的敏感性和特异性,(2)评估Cyfra 21-1与NSCLC疾病分期之间的潜在关系,(3)评估Cyfra 21-1在NSCLC中的预后作用。
对161例肺癌患者和71例其他良性肺病患者进行血清Cyfra 21-1的免疫放射分析。通过受试者操作特征(ROC)曲线以及与其他肿瘤标志物如癌胚抗原、神经元特异性烯醇化酶和鳞状细胞癌抗原的比较,评估Cyfra 21-1检测肺癌不同组织学亚型与良性肺病的能力。根据组织学亚型和疾病分期对Cyfra 21-1水平进行比较,采用Kruskal-Wallis检验。通过生存多因素分析(Cox模型)研究Cyfra 21-1的独立预后价值。
以Cyfra 21-1的阈值为3.3 ng/mL,在NSCLC中敏感性和特异性分别为0.59和0.94,在鳞状细胞癌亚组中为0.68和0.94,在小细胞肺癌中为0.19和0.94。晚期NSCLC患者的Cyfra 21-1水平显著高于早期疾病患者。所有29例血清浓度>32 ng/mL的患者均为ⅢB-IV期,而14例Ⅰ-II期疾病患者中只有1例Cyfra 21-1水平>18 ng/mL。在生存多因素分析中,Cyfra 21-1与NSCLC患者的体能状态和疾病分期一样,是一个独立的预后因素。
Cyfra 21-1是NSCLC尤其是鳞状细胞亚型的敏感和特异性肿瘤标志物。它还反映了疾病的程度,并且在NSCLC中与体能状态和疾病分期一样具有独立的预后作用。
在明显早期的NSCLC中,Cyfra 21-1水平升高应提示在开胸手术前进行更广泛的检查。Cyfra 21-1水平的独立预后作用可能有助于对晚期NSCLC或早期切除的NSCLC患者进行分层,因为Cyfra 21-1水平升高可能识别出那些治疗失败风险高的患者。