Can initial serum Cyfra 21-1, SCC antigen, and TPA levels in squamous cell cervical cancer predict lymph node metastases or prognosis?

被引:102
作者
Gaarenstroom, KN [1 ]
Kenter, GG
Bonfrer, JMG
Korse, CM
Van de Vijver, MJ
Fleuren, GJ
Trimbos, JB
机构
[1] Leiden Univ, Dept Gynecol, NL-2300 RC Leiden, Netherlands
[2] Leiden Univ, Dept Pathol, NL-2300 RC Leiden, Netherlands
[3] Netherlands Canc Inst, Dept Clin Chem, Amsterdam, Netherlands
关键词
cervical cancer; Cyfra; 21-1; TPA; SCC-Ag; serum markers; lymph node metastases; prognosis;
D O I
10.1006/gyno.2000.5732
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Objective. The aim of this study was to determine whether lymph node metastases or prognosis can be predicted by initial serum Cyfra 21-1, tissue polypeptide antigen (TPA), and squamous cell carcinoma antigen (SCC-Ag) levels in squamous cell cervical cancer. Methods. Pretreatment serum levels of 92 patients were correlated with clinicopathologic parameters and prognostic data. The clinical performance of the tests was evaluated by their receiver operating characteristic curves. The prognostic power of the variables was assessed using Cox regression analysis. Results. Serum levels of each marker were significantly related to tumor stage, size, and depth of infiltration. The clinical performance of each marker in predicting lymph node metastases or parametrial involvement was poor. In the stepwise Cox regression analysis, regarding patients with early stage cervical cancer (stage Ib/IIa, n = 63), tumor size (P = 0.0005) was the only independent prognostic factor for disease-free interval, Lymph node status (P = 0.0014), tumor size (P = 0.004), and parametrial involvement (P = 0.025) were independent risk factors for survival. Considering all patients with stages la through IVb disease, tumor size (P = 0.0001) and TPA level (P = 0.026) were independent risk factors for disease-free interval, whereas tumor size (P = 0.0001) and parametrial involvement (P = 0.0002) were risk factors for survival. Conclusions. Pretreatment Cyfra 21-1, TPA, and SCC-Ag levels were strongly related to tumor burden, but insufficiently reliable for identifying patients at risk of the presence of lymph node metastases or parametrial involvement. Serum levels of each marker showed no independent prognostic value in early stage cervical cancer. (C) 2000 Academic Press.
引用
收藏
页码:164 / 170
页数:7
相关论文
共 36 条
[1]
PROGNOSTIC-SIGNIFICANCE OF PRETREATMENT SERUM LEVELS OF SQUAMOUS-CELL CARCINOMA ANTIGEN AND CA125 IN CERVICAL-CARCINOMA [J].
AVALLLUNDQVIST, EH ;
SJOVALL, K ;
NILSSON, BR ;
ENEROTH, PHE .
EUROPEAN JOURNAL OF CANCER, 1992, 28A (10) :1695-1702
[2]
CORRELATION BETWEEN PATHOLOGICAL RISK-FACTORS AND PELVIC LYMPH-NODE METASTASES IN STAGE-I SQUAMOUS CARCINOMA OF THE CERVIX - A MULTIVARIATE-ANALYSIS OF 194 CASES [J].
AYHAN, A ;
TUNCER, ZS ;
KUCUKALI, T ;
TUNA, T ;
ENUNLU, T .
JOURNAL OF SURGICAL ONCOLOGY, 1991, 48 (03) :207-209
[3]
Prognostic significance of pretreatment squamous cell carcinoma antigen and carcinoembryonic antigen in squamous cell carcinoma of the uterine cervix [J].
Bae, SN ;
Namkoong, SE ;
Jung, JK ;
Kim, CJ ;
Park, JS ;
Kim, JW ;
Lee, JM ;
Kim, SJ .
GYNECOLOGIC ONCOLOGY, 1997, 64 (03) :418-424
[4]
Prognostic value of preoperative squamous cell carcinoma antigen level in patients surgically treated for cervical carcinoma [J].
Bolger, BS ;
Dabbas, M ;
Lopes, A ;
Monaghan, JM .
GYNECOLOGIC ONCOLOGY, 1997, 65 (02) :309-313
[5]
SQUAMOUS-CELL CARCINOMA ANTIGEN - CLINICAL UTILITY IN SQUAMOUS-CELL CARCINOMA OF THE UTERINE CERVIX [J].
BOLLI, JAN ;
DOERING, DL ;
BOSSCHER, JR ;
DAY, TG ;
RAO, CV ;
OWENS, K ;
KELLY, B ;
GOLDSMITH, J .
GYNECOLOGIC ONCOLOGY, 1994, 55 (02) :169-173
[6]
SQUAMOUS-CELL CARCINOMA ANTIGEN (SCC-A) VALUES RELATED TO CLINICAL OUTCOME OF PREINVASIVE AND INVASIVE CERVICAL-CARCINOMA [J].
BRIOSCHI, PA ;
BISCHOF, P ;
DELAFOSSE, C ;
KRAUER, F .
INTERNATIONAL JOURNAL OF CANCER, 1991, 47 (03) :376-379
[7]
Callet N, 1998, EUR J GYNAECOL ONCOL, V19, P50
[8]
CHOU CY, 1994, CANCER, V74, P2497, DOI 10.1002/1097-0142(19941101)74:9<2497::AID-CNCR2820740917>3.0.CO
[9]
2-L
[10]
COX DR, 1972, J R STAT SOC B, V34, P187