Webb A, Scott-Mackie P, Cunningham D, Norman A, Andreyev J, O'Brien M, Bensted J
Cancer Research Campaign Section of Medicine, Royal Marsden Hospital, Sutton, Surrey, U.K.
Eur J Cancer. 1996 Jan;32A(1):63-8. doi: 10.1016/0959-8049(95)00504-8.
Using a prospectively acquired database of 290 patients with advanced gastric adenocarcinoma, the prognostic significance of serum levels of carcinoembryonic antigen (CEA) (237 patients), alphafeto protein (AFP) (164 patients), beta-human chorionic gonadotrophin (beta HCG) (165 patients), CA19-9 (64 patients) and CA125 (104 patients) and tissue staining for C-erb B-2 (160 patients) and beta HCG (160 patients) was investigated. Serum was taken prior to 5-fluorouracil (5FU)-based chemotherapy and immunohistochemistry was performed on diagnostic specimens. In the univariate analysis, tumour markers of poor prognosis were CEA > or = 5 micrograms/l (P = 0.01; median survival (MS) 42 versus 35 weeks), serum beta HCG > or = 4 U/l (P = 0.02; MS 42 versus 25 weeks), CA125 > or = 35 U/ml (P = 0.03; MS 43 versus 31 weeks) and CA125 > or = 350 U/ml (P = 0.001; MS 42 versus 17 weeks). Other significant factors were poor performance status, the presence of metastases and poorly differentiated tumour histology. Tumours markers of poor prognosis in the multivariate analysis were serum beta HCG > or = 4 IU/l [hazard ratio (HR) 1.7; 95% confidence interval (CI) 2.8-1.1] and CA125 > or = 350 U/ml (HR 2.2; CI 4.2-1.2). There was a degree of subgroup variability in this model but, in general, other factors correlating with a poor survival were poor performance status, metastases and poorly differentiated tumour histology. This is the largest prognostic study of each tumour marker in advanced disease and demonstrates that serum beta HCG and CA125 in gastric cancer prior to chemotherapy do convey an independent poor prognosis which may reflect not just tumour burden but aggressive biology.
利用前瞻性收集的290例晚期胃腺癌患者的数据库,研究了癌胚抗原(CEA)(237例患者)、甲胎蛋白(AFP)(164例患者)、β-人绒毛膜促性腺激素(β-HCG)(165例患者)、CA19-9(64例患者)和CA125(104例患者)的血清水平以及C-erb B-2(160例患者)和β-HCG(160例患者)的组织染色的预后意义。在基于5-氟尿嘧啶(5FU)的化疗前采集血清,并对诊断标本进行免疫组织化学检测。单因素分析中,预后不良的肿瘤标志物为CEA≥5微克/升(P = 0.01;中位生存期(MS)42周对35周)、血清β-HCG≥4 U/升(P = 0.02;MS 42周对25周)、CA125≥35 U/毫升(P = 0.03;MS 43周对31周)和CA125≥350 U/毫升(P = 0.001;MS 42周对17周)。其他显著因素为体能状态差、存在转移和肿瘤组织学分化差。多因素分析中,预后不良的肿瘤标志物为血清β-HCG≥4 IU/升[风险比(HR)1.7;95%置信区间(CI)2.8 - 1.1]和CA125≥350 U/毫升(HR 2.2;CI 4.2 - 1.2)。该模型存在一定程度的亚组变异性,但总体而言,与生存不良相关的其他因素为体能状态差、转移和肿瘤组织学分化差。这是对晚期疾病中每种肿瘤标志物进行的最大规模预后研究,表明化疗前胃癌患者血清β-HCG和CA125确实预示着独立的不良预后,这可能不仅反映肿瘤负荷,还反映侵袭性生物学行为。