Serum ferritin as a clinical marker for renal cell carcinoma: Influence oftumor size and volume

Citation
Z. Kirkali et al., Serum ferritin as a clinical marker for renal cell carcinoma: Influence oftumor size and volume, UROL INTERN, 62(1), 1999, pp. 21-25
Citations number
16
Categorie Soggetti
Urology & Nephrology
Journal title
UROLOGIA INTERNATIONALIS
ISSN journal
00421138 → ACNP
Volume
62
Issue
1
Year of publication
1999
Pages
21 - 25
Database
ISI
SICI code
0042-1138(1999)62:1<21:SFAACM>2.0.ZU;2-G
Abstract
Objectives: There is no established tumor marker for renal cell carcinoma ( RCC). Ferritin is shown to be expressed by the tumor, and proposed as a tum or marker. The aim of this study is to assess the relation between ferritin levels and tumor volume, size and prognosis in RCC. Methods: We studied fe rritin levels in serum from peripheral and renal veins of 52 patients with RCC who underwent surgery. Ferritin levels were measured by an enzyme immun oassay method. Tumor volume and the largest tumor diameter were calculated from the pathologic specimens. Results: The mean serum ferritin level from the renal vein (RVF) was statistically higher than the ferritin level from the peripheral vein (PVF) (p = 0.028). Although mean RVF level increased wi th increasing stage, it was not significant. While there was a correlation with tumor size, volume and RVF, PVF was in correlation with disease status . PVF in patients with metastatic and/or locally advanced disease was signi ficantly higher than the patients with localized disease (p = 0.023), The i nitial RVF and PVF levels were predictive of survival (p = 0.028 and p = 0. 034, respectively). Conclusions: Higher levels in the renal vein, its posit ive correlation with tumor size and volume suggest that ferritin is express ed by RCC. Initial peripheral serum values of ferritin can be indicative of disease status and also be a prognosticator of survival.