Clinical application of proliferating cell nuclear antigen, oncoprotein p53 and tumor front grading analysis in patients operated on for laryngeal cancer

Citation
K. Morawski et al., Clinical application of proliferating cell nuclear antigen, oncoprotein p53 and tumor front grading analysis in patients operated on for laryngeal cancer, EUR ARCH OT, 256(8), 1999, pp. 378-383
Citations number
31
Categorie Soggetti
Otolaryngology
Journal title
EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY
ISSN journal
09374477 → ACNP
Volume
256
Issue
8
Year of publication
1999
Pages
378 - 383
Database
ISI
SICI code
0937-4477(199909)256:8<378:CAOPCN>2.0.ZU;2-Q
Abstract
The authors assessed proliferating cell nuclear antigen (PCNA), p-53 oncopr otein and morphologic tumor front grading (TFG) in patients with advanced s quamous cell carcinoma (SCC), of the larynx and a poor prognosis and tried to find a correlation with tumor stage, the Broders grading system, local a nd neck lymph node metastases, as well as nodal and local recurrences. in a ddition, utility of the parameters investigated was evaluated in developing a prognostic factor model, using uni- and multivariate Cox regression anal ysis. included in this study were 54 patients (mean age 57 years +/- 8.6). PCNA-positive staining was found in all but one patient with advanced disea se. while p-53 stained positively in only 24 subjects (44.4%). The PCNA ind ex ranged from 4.6 to 59.0% (mean, 23.4 +/- 11.0) and the p-53 index varied from 4.0 to 42.0% (mean, 17.2 +/- 8.6). The TFG score ranged from 9 to 23 points (mean, 15.1 +/- 3.2). PCNA, p-53 and TFG were found to be the marker s that provided significant additional information about the biological beh avior of tumor cells. The high variability of the results (PCNA, p53) and h igh percentage of negatively stained cells (p-53) reduced their application in clinical use. PCNA correlated with tumor grade, G (r = 0.38; P < 0.01), but negatively with nodal (N) disease(r = -0.37, P < 0.01). The mean value s of PCNA and p-53 index were higher in the subgroup with local recurrences . Our present attempt to develop a useful prognostic factor model failed.