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Association and prognostic value of serum inflammation markers in patients with leukoplakia and oral cavity cancer

  • Pi-Yueh Chang , Yung-Bin Kuo , Tsu-Lan Wu , Chun-Ta Liao , Yu-Chen Sun , Tzu-Chen Yen and Err-Cheng Chan EMAIL logo
Published/Copyright: November 15, 2012

Abstract

Background: Oral cavity cancer ranks as the fourth leading cancer in men in Taiwan. The development of a serum biomarker panel for early detection and disease monitoring is, therefore, warranted.

Methods: Nine inflammation-associated markers were investigated in 46 patients with leukoplakia, 151 patients with untreated oral cavity squamous cell carcinoma (OSCC), and 111 age- and gender-matched healthy controls using enzyme-linked immunosorbent assay. During a subsequent 28-month surveillance of OSCC patients, serum samples were prospectively collected at predetermined intervals following the completion of therapy.

Results: Logistic regression analysis showed matrix metalloproteases (MMP)-2, MMP-9, C-reactive protein (CRP), transforming growth factor-β1 (TGF-β1), and E-selectin having the best discrimination power between groups and significant elevation trends of those five markers were noted from control to OSCC. By combining those five markers, a 0.888 and 0.938 area under curve by ROC curve analysis with 67.4% and 80% overall sensitivity and fixed 90% specificity for leukoplakia and OSCC groups were demonstrated. In the follow-up period, 25 OSCC patients developed recurring or secondary tumors. All examined markers had decreased in relapse-free patients following treatment. However, in patients with relapse, interleukin-6, CRP, and serum amyloid A remained at elevated levels. Statistical analysis showed that patients with CRP ≧2 mg/L and E-selectin ≧85 ng/mL at baseline had highest probability of relapse (odds ratio=3.029, p<0.05).

Conclusions: The results indicate that inflammation plays a crucial role in the pathogenesis process of OSCC. By examining the inflammation markers, physicians could potentially identify patients at risk of cancer transformation or relapse.


Corresponding author: Err-Cheng Chan, Department of Medical Biotechnology and Laboratory Science, Chang Gung University, 259 Wen-Hua 1st Road, Kwei-shan, Taoyuan, Taiwan, Republic of China Phone: +886 3 2118800 ext. 5220, Fax: +886 3 2118741

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Received: 2012-08-03
Accepted: 2012-10-04
Published Online: 2012-11-15
Published in Print: 2013-06-01

©2013 by Walter de Gruyter Berlin Boston

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