The prognostic significance of the biomarkers p21WAF1/CIP1, p53, and bcl-2 in laryngeal squamous cell carcinoma

被引:0
|
作者
Jin, YT
Kayser, S
Kemp, BL
Ordonez, NG
Tucker, SL
Clayman, GL
Goepfert, H
Luna, MA
Batsakis, JG
El-Naggar, AK
机构
[1] Univ Texas, MD Anderson Cancer Ctr, Dept Pathol, Houston, TX 77030 USA
[2] Natl Cheng Kung Univ, Med Ctr, Dept Pathol, Tainan 70101, Taiwan
[3] Univ Texas, MD Anderson Cancer Ctr, Dept Head & Neck Surg, Houston, TX 77030 USA
[4] Univ Texas, MD Anderson Cancer Ctr, Dept Biomath, Houston, TX 77030 USA
关键词
suppressor genes; biomarkers; squamous cell carcinoma; larynx; flow cytometry; oncogenesis;
D O I
10.1002/(SICI)1097-0142(19980601)82:11<2159::AID-CNCR10>3.0.CO;2-T
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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, p21(WAF1/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 p21(WAF1/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. (C) 1998 American Cancer Society.
引用
收藏
页码:2159 / 2165
页数:7
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