Journal
HISTOPATHOLOGY
Volume 63, Issue 2, Pages 242-249Publisher
WILEY
DOI: 10.1111/his.12151
Keywords
maspin; prognosis; subcellular location; targeted therapy; temporal bone carcinoma
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Funding
- University of Padova, Italy [60A07-1341/12]
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AimsAlthough it accounts for fewer than 0.2% of all head and neck tumours, temporal bone squamous cell carcinoma (SCC) is an aggressive malignancy with a poor prognosis in advanced cases. Novel therapeutic strategies should be developed focusing on specific targeted therapies. Maspin is a serpin showing tumour-suppressing activity which has therapeutic potential. The present study is the first to investigate maspin expression in temporal bone SCCs, using a series of 29 cases. Methods and resultsCytoplasmic maspin expression was significantly higher in the group of patients whose SCC did not recur than in the group experiencing recurrences (P=0.029), and in G1-G2 SCCs than in G3 cases (P=0.001). cT correlated with recurrence rate (P=0.05), disease-free survival (DFS) (P=0.008) and disease-specific survival (DSS) (P=0.0043), and pT and pathological regional lymph node status correlated with recurrence rate (P=0.008 and P=0.03, respectively), DFS (P= 0.017 and P=0.0049, respectively) and DSS (P=0.008 and P=0.0009, respectively). ConclusionsAlthough further studies using larger series are required, our preliminary findings suggest that cytoplasmic maspin expression has promise as a prognostic indicator of disease recurrence in temporal bone SCC, and that reactivating maspin functions in association with apoptosis-inducing or anti-angiogenic chemotherapeutic agents might be an important goal in the treatment of temporal bone SCC.
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