The prognostic significance of the biomarkers p21WAF1/CIP1, p53, andbcl-2 in laryngeal squamous cell carcinoma
Autor: | Ying Tai Jin, Adel K. El-Naggar, Helmuth Goepfert, John G. Batsakis, Mario A. Luna, Nelson G. Ordóñez, Bonnie L. Kemp, Susan L. Tucker, Scott Kayser, Gary L. Clayman |
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Rok vydání: | 1998 |
Předmět: |
Biologic marker
Oncology Cancer Research Univariate analysis Pathology medicine.medical_specialty Multivariate analysis business.industry Cancer medicine.disease_cause medicine.disease medicine.anatomical_structure Epidermoid carcinoma Internal medicine Carcinoma Medicine business Carcinogenesis Lymph node |
Zdroj: | Cancer. 82:2159-2165 |
ISSN: | 1097-0142 0008-543X |
DOI: | 10.1002/(sici)1097-0142(19980601)82:11<2159::aid-cncr10>3.0.co;2-t |
Popis: | BACKGROUND The clinical course of laryngeal squamous cell carcinoma (LSCC) varies considerably among patients. New biologic markers are needed to facilitate the stratification of individual patients within the conventional clinicopathologic stages of LSCC. METHODS Eighty-three LSCCs from an equal number of patients who received at least 10 years of follow-up were investigated for p53, p21WAF1/CIP1, and bcl-2 protein expression by immunohistochemical techniques. The results were correlated with various clinicopathologic parameters, DNA content, and patient outcome by univariate and multivariate statistical analyses. RESULTS Stage IV disease, large tumor size (>3 cm), positive lymph node status, extranodal extension, and p53 overexpression (in > 75% of cells) correlated significantly with prognosis in univariate analysis. There was no correlation between patient outcome and age, gender, race, histologic differentiation, or expression of bcl-2 or p21WAF1/CIP1. In multivariate analysis, lymph node status and p53 overexpression were the only factors significantly associated with survival. CONCLUSIONS High p53 expression and positive lymph node status were independent predictors of the outcomes of patients with LSCC. These factors may assist in prognostication and better classification of patients for treatment. Cancer 1998;82:2159-2165. © 1998 American Cancer Society. |
Databáze: | OpenAIRE |
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