Serum Protein S-100 Predicts Clinical Outcome in Patients with Melanoma Treated with Adjuvant Interferon – Comparison with Tyrosinase RT-PCR

Objective: To study the clinical value of the determination of serum S-100 protein as a single tumor marker or in combination with tyrosinase RT-PCR in patients with melanoma receiving adjuvant interferon. Patients and Methods: Patients were tested for serum S-100 protein luminoimmunometric assay an...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Oncology 2005-01, Vol.68 (4-6), p.341-349
Hauptverfasser: Domingo-Domènech, J., Molina, R., Castel, T., Montagut, C., Puig, S., Conill, C., Martí, R., Vera, M., Auge, J.M., Malvehy, J., Grau, J.J., Gascón, P., Mellado, B.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Objective: To study the clinical value of the determination of serum S-100 protein as a single tumor marker or in combination with tyrosinase RT-PCR in patients with melanoma receiving adjuvant interferon. Patients and Methods: Patients were tested for serum S-100 protein luminoimmunometric assay and for blood tyrosinase mRNA (RT-PCR), before starting interferon and every 2–3 months thereafter. Results: One hundred and six patients (stage IIA, 27; IIB, 19; III, 49; and IV, 11) were included in the study. Median follow-up was 51 months (range 2–76). In the univariate analysis, under treatment S-100 ≧0.15 µg/l and a positive RT-PCR correlated with a lower disease-free survival and overall survival (OS). In the multivariate analysis, clinical stage, under therapy positive RT-PCR and S-100 levels ≧0.15 µg/ml, were independent prognostic factors for OS. The hazard ratio for OS was 3.9 (95% CI, 1.67–9.15; p = 0.004) and 2.2 (95% CI, 1.05–4.6; p = 0.016) for S-100 ≧0.15 µg/l and positive RT-PCR, respectively. When both techniques where combined, a positive RT-PCR indicated a poorer clinical outcome only in patients with S-100
ISSN:0030-2414
1423-0232
DOI:10.1159/000086973