AI Article Synopsis

  • Adjuvant cisplatin-based chemoradiation significantly improves survival rates for head and neck squamous cell carcinoma (HNSCC) patients with risk features.
  • The study focused on ERCC1 (excision repair cross-complementation group 1) as a potential marker for prognosis, assessing ERCC1 protein and mRNA expression alongside the T19007C polymorphism.
  • Results indicated that higher ERCC1 protein and mRNA levels were associated with better 5-year overall survival rates, suggesting that ERCC1 expression could be an important prognostic factor for HNSCC patients undergoing treatment.

Article Abstract

Adjuvant cisplatin-based chemoradiation improves survival in HNSCC patients presenting with risk features. ERCC1 (excision repair cross-complementation group 1) is associated with resistance to chemo- and radiation therapy and may have a prognostic value in HNSCC patients. Here we studied ERCC1 expression and the polymorphism T19007C as prognostic markers in these patients. This is a retrospective and translational analysis, where ERCC1 protein expression was evaluated by immunohistochemistry, using an H-score, and mRNA expression was determined by RT-PCR. T19007C genotypes were detected by PCR-RFLP carried out using DNA template extracted from normal lymph nodes. A high H-score was seen in 32 patients (54%), who presented better 5-year overall survival (5-y OS: 50% vs. 18%, HR 0.43, p=0.026). Fifteen out of 45 patients (33%), with high mRNA expression, presented better 5-year overall survival (OS) (86% vs. 30%, HR 0.26, p=0.052). No OS difference was detected among T19007C genotypes. High H-score and mRNA expression remained significant as favorable prognostic factors in a multivariate analysis. Collectively, our results suggest that high ERCC1 expression seems to be associated with better OS rates in HNSCC patients submitted to adjuvant cisplatin-based chemoradiation.

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Source
http://dx.doi.org/10.3892/or.2011.1133DOI Listing

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