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

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:...

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Veröffentlicht in:Lung cancer (Amsterdam, Netherlands) Netherlands), 2002-06, Vol.36 (3), p.265-270
Hauptverfasser: Reinmuth, Niels, Brandt, Burkhard, Semik, Michael, Kunze, Wolf-Peter, Achatzy, Richard, Scheld, Hans H., Broermann, Petra, Berdel, Wolfgang E., Macha, Hans N., Thomas, Michael
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Sprache:eng
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Zusammenfassung: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 serum 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.
ISSN:0169-5002
1872-8332
DOI:10.1016/S0169-5002(02)00009-0