Pujol J L, Cooper E H, Lehmann M, Purves D A, Dan-Aouta M, Midander J, Godard P, Michel F B
Service des Maladies Respiratoires, Université de Montpellier, Hôpital Arnaud de Villeneuve, France.
Br J Cancer. 1993 Jun;67(6):1423-9. doi: 10.1038/bjc.1993.264.
CA 242, a novel tumour carbohydrate antigen present in serum (upper limit of normal values: 20.0 U ml-1), has been measured in a group of 102 pathologically confirmed non-small cell lung cancer patients. The aim of the present prospective study was to identify any relationship between pre-treatment serum CA 242 level and different features of lung cancer including prognosis. Serum CA 242 was measured using the delayed europium lanthanide fluoroimmunometric assay. Sensitivity and specificity were 28.5% and 95.6% respectively. Its level was significantly lower in squamous cell carcinoma in comparison with non-squamous histologies (adenocarcinoma and large cell carcinoma). The CA 242 level was higher in metastatic disease (median: 15.3 U ml-1) in comparison with non-metastatic (median: 7.9 U ml-1; Mann Whitney U test; P < 0.003), and increased significantly from stage I to stage IV. In 50 patients who underwent chemotherapy, the serum CA 242 level was higher in non-responder patients when compared with responders (median: 16.8 U ml-1 and 9.5 U ml-1 respectively; Mann Whitney; P < 0.02). Univariate analysis of the entire population showed serum CA 242 levels were not related to survival. However, patients with unresectable non-small cell lung cancer and elevated CA 242 level proved to have a significantly shorter survival than those with a CA 242 < 20 U ml-1. In Cox's model analysis, stage of the disease and performance status were the only significant determinants of survival. We conclude that a high level of serum CA 242 (1) is significantly related to the stage of disease, (2) predictive of no response to chemotherapy but seems to add weak prognostic information to stage of disease and performance status, the main prognostic determinants of non-small cell lung cancer.
CA 242是一种存在于血清中的新型肿瘤碳水化合物抗原(正常值上限:20.0 U/ml),已在一组102例经病理确诊的非小细胞肺癌患者中进行了检测。本前瞻性研究的目的是确定治疗前血清CA 242水平与肺癌不同特征(包括预后)之间的关系。采用延迟铕镧荧光免疫分析法检测血清CA 242。敏感性和特异性分别为28.5%和95.6%。与非鳞状组织学类型(腺癌和大细胞癌)相比,其在鳞状细胞癌中的水平显著较低。与非转移性疾病(中位数:7.9 U/ml;Mann-Whitney U检验;P<0.003)相比,转移性疾病中的CA 242水平更高(中位数:15.3 U/ml),且从I期到IV期显著升高。在50例接受化疗的患者中,与有反应者相比,无反应者的血清CA 242水平更高(分别为中位数:16.8 U/ml和9.5 U/ml;Mann-Whitney检验;P<0.02)。对整个人群的单因素分析显示血清CA 242水平与生存无关。然而,不可切除的非小细胞肺癌且CA 242水平升高的患者的生存期明显短于CA 242<20 U/ml的患者。在Cox模型分析中,疾病分期和体能状态是生存的唯一重要决定因素。我们得出结论,血清CA 242高水平(1)与疾病分期显著相关,(2)预示对化疗无反应,但似乎仅为非小细胞肺癌的主要预后决定因素——疾病分期和体能状态增加了微弱的预后信息。