Prognostic impact of RITA expression in patients with anal squamous cell carcinoma treated with chemoradiotherapy

RBP-J interacting and tubulin-associated protein (RITA) has been identified as a negative regulator of the Notch signalling pathway and its deregulation is involved in the pathogenesis of several tumour entities. RITA’s impact on the response of anal squamous cell carcinoma (SCC) to anticancer treat...

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Veröffentlicht in:Radiotherapy and oncology 2018-02, Vol.126 (2), p.214-221
Hauptverfasser: Rödel, Franz, Steinhäuser, Kerstin, Kreis, Nina-Naomi, Friemel, Alexandra, Martin, Daniel, Wieland, Ulrike, Rave-Fränk, Margret, Balermpas, Panagiotis, Fokas, Emmanouil, Louwen, Frank, Rödel, Claus, Yuan, Juping
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Sprache:eng
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Zusammenfassung:RBP-J interacting and tubulin-associated protein (RITA) has been identified as a negative regulator of the Notch signalling pathway and its deregulation is involved in the pathogenesis of several tumour entities. RITA’s impact on the response of anal squamous cell carcinoma (SCC) to anticancer treatment, however, remains elusive. In our retrospective study immunohistochemical evaluation of RITA was performed on 140 pre-treatment specimens and was correlated with clinical and histopathologic characteristics and clinical endpoints cumulative incidence of local control (LC), distant recurrence (DC), disease-free survival (DFS) and overall survival (OS). We observed significant inverse correlations between RITA expression and tumour grading, the levels of HPV-16 virus DNA load, CD8 (+) tumour infiltrating lymphocytes and programmed death protein (PD-1) immunostaining. In univariate analyses, elevated levels of RITA expression were predictive for decreased local control (p = 0.001), decreased distant control (p = 0.040), decreased disease free survival (p = 0.001) and overall survival (p 
ISSN:0167-8140
1879-0887
DOI:10.1016/j.radonc.2017.10.028