Prognostic impact of Cyfra21-1 and other serum markers in completely resected non-small cell lung cancer

被引:100
作者
Reinmuth, N
Brandt, B
Semik, M
Kunze, WP
Achatzy, R
Scheld, HH
Broermann, P
Berdel, WE
Macha, HN
Thomas, M
机构
[1] Univ Munster, Dept Med Haematol & Oncol & Resp Med, D-48129 Munster, Germany
[2] Univ Munster, Dept Lab Med, D-48129 Munster, Germany
[3] Univ Munster, Dept Thorac & Cardiovasc Surg, D-48129 Munster, Germany
[4] Lungenklin, Dept Thorac Surg, Hemer, Germany
[5] Lungenklin, Dept Pneumol, Hemer, Germany
关键词
non-small cell lung cancer; Cyfra21-1; prognostic factor; prospective study; long-term follow-up; early stage disease;
D O I
10.1016/S0169-5002(02)00009-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: The aim of this prospective study was to assess the prognostic impact of serum tumor markers (Cyfra21-1, carcinoembryonic antigen, neuron-specific enolase, squamous cell carcinoma-antigen and TPAcyk) in patients with non-small cell lung cancer (NSCLC) receiving complete resection. Methods: Sixty-seven patients with histologically proven NSCLC and complete resection of stage I-IIIA disease were included. The scrum levels of all markers were measured using commercially available immunoassays. Results: With a median follow-up of 86 months for surviving patients, those with initial Cyfra21-1 serum levels higher than 3.57 ng/ml had a significantly worse prognosis (P=0.014). The remaining serum tumor markers showed no prognostic impact. In a Cox regression model, Cyfra21-1 proved to be an independent prognostic factor for both overall survival and disease-free interval. In addition, Cyfra21-1 sustained as an independent prognostic factor in completely resected stage I/II disease. Conclusions: With a cut-off value of 3.57 ng/ml, Cyfra 21-1 was an independent prognostic factor for survival in NSCLC-patients with complete resection. Further evaluation is needed, particularly in stage I/II disease. When the prognostic impact is confirmed with larger patient numbers this may contribute to the identification of stratification variables for future treatment approaches of NSCLC. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:265 / 270
页数:6
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