AI Article Synopsis

  • Oral cavity cancers (ORC) are the most common type of cancer, with current treatments often involving radical surgery and radiotherapy. However, there is a persistent issue of radioresistance leading to high rates of locoregional failure. The study examines the role of GP96, a protein associated with radioresistance, in the prognosis of ORC patients undergoing radiotherapy.
  • The study included 79 ORC patients who underwent radical surgery and radiotherapy, with findings showing that 70% had high GP96 levels in their tumor tissues. This overexpression of GP96 correlated with worse clinical outcomes, including higher tumor stages and depth, and was linked to reduced rates of locoregional control and overall survival.
  • The

Article Abstract

Background: Oral cavity cancers (ORC) are the most common cancers, and standard treatment is radical surgery with postoperative radiotherapy. However, locoregional failure remains a major problem, indicating radioresistance an important issue. Our previous work has shown that GP96 contributed to radioresistance in nasopharyngeal and oral cancer cell lines. In this study, we determined clinical significance of GP96 in ORC by evaluation of GP96 expression and its association with disease prognosis in patients receiving radiotherapy

Methods: Total of 79 ORC patients (77 males, median age: 48 years old) receiving radical surgery and postoperative radiotherapy between Oct 1999 and Dec 2004 were enrolled. Patients in pathological stages II, III and IV were 16.5%, 16.5% and 67%, respectively. For each patient, a pair of carcinoma tissue and grossly adjacent normal mucosa was obtained. GP96-expression was examined by western blot analysis, and the association with clinicopathological status was determined.

Results: Three-year locoregional control (LRC), distant metastasis-free survival (DMFS), disease-specific survival (DSS) and overall survival (OS) rates were 69%, 79%, 63% and 57%, respectively. We found that 55 patients (70%) displayed GP96-overexpression in the tumor tissue, which correlated with a higher pN stage (p = 0.020) and tumor depth (> 10 mm) (p = 0.045). Nodal extracapsular spreading (ECS) and GP96-overexpression predicted adverse LRC (p = 0.049 and p = 0.008). When stratified by nodal ECS, the adverse impact of GP96 remained significant in three-year LRC (p = 0.004). In multivariate analysis, GP96-overexpression was also an independent predictor of LRC, DSS and OS (p = 0.018, p = 0.011 and p = 0.012).

Conclusion: GP96 may play roles in radioresistance which attributes to tumor invasiveness in oral cancer patients receiving radiotherapy. GP96 may serve as a novel prognostic marker of radiotherapy. However, further independent studies are required to validate our findings in a larger series.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3214142PMC
http://dx.doi.org/10.1186/1748-717X-6-136DOI Listing

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