Prognosis in bronchogenic squamous cell carcinoma groups divided according to serum squamous cell carcinoma-related antigen and cytokeratin 19 fragment levels

被引:13
作者
Kashiwabara, K
Nakamura, H
Esaki, T
机构
[1] Taragi Municipal Hosp, Resp Dept, Kumamoto 8680501, Japan
[2] Univ Tokyo, Dept Internal Med 5, Tokyo, Japan
关键词
lymph node metastasis; distant metastasis; indication for surgery; two-year survival rates; carcinoembryonic antigen;
D O I
10.1016/S0009-8981(99)00247-8
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
We examined differences in the 2-year survival rate in bronchogenic squamous cell carcinoma patients with normal serum levels of both cytokeratin 19 fragment (CYFRA 21-1) and squamous cell carcinoma-related antigen (SCC) (NL group, n = 15), patients with only increased SCC levels (SCC + group, n = 14), patients with only increased CYFRA 21-1 levels (CYFRA + group, n = 14), and patients with elevated levels of both CYFRA 21-1 and SCC (EL group, n = 65). The 2-year survival rates for the CYFRA + and the EL group were lower than those for the SCC + group and the NL group (0 and 12.9% vs. 66.7 and 85.6%, log rank: p < 0.0001, Wilcoxon: p < 0.0001). However, there were no differences between the rate for the SCC + and the NL group and between that for the CYFRA + and the EL group. Serum carcinoembryonic antigen (CEA) levels increased in the patients with the elevated CYFRA 21-1 levels. This results suggest that there may be some differences between squamous cell carcinoma patients with increased CYFRA 21-1 levels and those with normal levels and that it is CYFRA 21-1 levels, not SCC levels, that relate to the prognosis. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:105 / 113
页数:9
相关论文
共 21 条
[1]  
BODY JJ, 1990, CANCER, V65, P1552, DOI 10.1002/1097-0142(19900401)65:7<1552::AID-CNCR2820650717>3.0.CO
[2]  
2-D
[3]   SQUAMOUS-CELL CARCINOMA ANTIGEN (SCC AG) IN THE DIAGNOSIS AND PROGNOSIS OF LUNG-CANCER [J].
DECOS, JS ;
MASA, F ;
DELACRUZ, JL ;
DISDIER, C ;
VERGARA, C .
CHEST, 1994, 105 (03) :773-776
[4]  
EBERT W, 1994, EUR J CLIN CHEM CLIN, V32, P189
[5]  
Ebert W, 1996, ANTICANCER RES, V16, P2161
[6]  
KATO H, 1977, CANCER, V40, P1621, DOI 10.1002/1097-0142(197710)40:4<1621::AID-CNCR2820400435>3.0.CO
[7]  
2-I
[8]  
KOGA H, 1994, JPN J CLIN ONCOL, V24, P263
[9]  
MOLINA R, 1990, CLIN CHEM, V36, P251
[10]  
Niklinski J, 1992, Eur J Cancer Prev, V1, P401, DOI 10.1097/00008469-199210000-00002