Burghuber O C, Worofka B, Schernthaner G, Vetter N, Neumann M, Dudczak R, Kuzmits R
2nd Medical Department, University of Vienna, Austria.
Cancer. 1990 Mar 15;65(6):1386-90. doi: 10.1002/1097-0142(19900315)65:6<1386::aid-cncr2820650623>3.0.co;2-9.
Small cell lung cancer (SCLC) may be potentially curable. A correct diagnosis of cancer cell type is important and serum markers are of great value. Although several markers have been suggested, they have been of limited value because of insufficient specificity. To assess the value of serum neuron-specific enolase (S-NSE) as a possible marker of SCLC, the serum levels of 81 patients with SCLC (59 patients with extensive disease and 22 patients with limited disease) were compared with the serum levels of patients with non-small cell lung cancer (N-SCLC) and 93 patients with nonmalignant lung diseases. The S-NSE level also was measured in 104 patients with extensive disease of various other malignancies, including 71 solid tumors and 33 malignant hematologic disorders. From 105 healthy control subjects, the upper limit of the normal range (x + 2 standard deviations [SD]) was determined as 12.3 ng/ml. The S-NSE level was elevated in 78% of patients with SCLC, including 11 of 22 (50%) with limited disease and 52 of 59 (88%) with extensive disease. In contrast, the S-NSE level was raised only in 18% of patients with advanced N-SCLC (nine of 50) and 6% of patients with nonmalignant lung diseases (six of 93). Twelve patients (17%) with other solid malignant tumors and two patients (6%) with malignant hematologic disorders had raised S-NSE levels. Serial N-NSE levels were obtained in 13 patients with SCLC. S-NSE levels fell in all patients responding to chemotherapy and increased again with progression of disease. Our results indicate that S-NSE seems to be specific for SCLC (85%), whereas sensitivity seems to be dependent on the stage of disease. Further, S-NSE may be a useful marker for monitoring treatment and predicting relapse in patients with SCLC.
小细胞肺癌(SCLC)可能具有潜在的可治愈性。准确诊断癌细胞类型很重要,血清标志物具有重要价值。尽管已经提出了几种标志物,但由于特异性不足,它们的价值有限。为了评估血清神经元特异性烯醇化酶(S-NSE)作为SCLC可能标志物的价值,将81例SCLC患者(59例广泛期患者和22例局限期患者)的血清水平与非小细胞肺癌(N-SCLC)患者以及93例非恶性肺部疾病患者的血清水平进行了比较。还对104例患有各种其他恶性肿瘤广泛期疾病的患者进行了S-NSE水平检测,其中包括71例实体瘤和33例恶性血液系统疾病。从105名健康对照受试者中,确定正常范围的上限(x + 2标准差[SD])为12.3 ng/ml。78%的SCLC患者S-NSE水平升高,其中22例局限期患者中有11例(50%),59例广泛期患者中有52例(88%)。相比之下,晚期N-SCLC患者中只有18%(50例中的9例)和非恶性肺部疾病患者中6%(93例中的6例)的S-NSE水平升高。12例(17%)其他实体恶性肿瘤患者和2例(6%)恶性血液系统疾病患者的S-NSE水平升高。对13例SCLC患者进行了连续的S-NSE水平检测。所有对化疗有反应的患者S-NSE水平均下降,随着疾病进展又再次升高。我们的结果表明,S-NSE似乎对SCLC具有特异性(85%),而敏感性似乎取决于疾病阶段。此外,S-NSE可能是监测SCLC患者治疗和预测复发的有用标志物。