Baumann M, Brand K, Giedl J, Hermanek P, Ruf S, Scheele J, Hoferichter S, Gall F P
Institute of Biochemistry, Medical Faculty, University of Erlangen-Nuremberg, FRG.
Oncology. 1988;45(3):153-8. doi: 10.1159/000226553.
The purpose of this study was to reevaluate the significance of serum PHI in gastrointestinal cancer at histopathologically defined stages prior to primary treatment. A total of 248 patients with malignant tumors of the gastrointestinal tract and a collective of 42 patients with noncancerous diseases were studied. The results are compared with those obtained with the established markers tissue polypeptide antigen (TPA) and carcinoembryonic antigen (CEA). Phosphohexose isomerase (PHI) revealed an overall diagnostic sensitivity of 69%, combined with a specificity of 74%. The corresponding data for TPA were found to be 73 and 47% while for CEA 26 and 95% respectively were determined. Even in the early stages of colorectal and esophageal carcinoma, PHI showed a sensitivity of about 60%. A continuous rise of PHI serum levels, correlating well with the extent of the tumor disease, could be detected. In contrast to TPA and CEA, PHI assay can be carried out with a minimum of laboratory efforts, in a short time and at low costs. These findings suggest that serum PHI assay is a useful aid for screening of gastrointestinal cancer, especially esophageal and gastric carcinoma, and a reliable marker for treatment control and follow-up.
本研究的目的是在初次治疗前,重新评估血清磷酸己糖异构酶(PHI)在组织病理学明确分期的胃肠道癌中的意义。共研究了248例胃肠道恶性肿瘤患者以及42例非癌性疾病患者。将结果与已确立的标志物组织多肽抗原(TPA)和癌胚抗原(CEA)的结果进行比较。磷酸己糖异构酶(PHI)的总体诊断敏感性为69%,特异性为74%。TPA的相应数据分别为73%和47%,而CEA分别为26%和95%。即使在结直肠癌和食管癌的早期阶段,PHI的敏感性也约为60%。可以检测到PHI血清水平持续升高,且与肿瘤疾病的程度密切相关。与TPA和CEA不同,PHI检测所需的实验室工作最少,耗时短且成本低。这些发现表明,血清PHI检测有助于筛查胃肠道癌,尤其是食管癌和胃癌,并且是治疗控制和随访的可靠标志物。