Immune inflammation indicators in anal cancer patients treated with concurrent chemoradiation: training and validation cohort with online calculator (ARC: Anal Cancer Response Classifier)

In anal cancer, there are no markers nor other laboratory indexes that can predict prognosis and guide clinical practice for patients treated with concurrent chemoradiation. In this study, we retrospectively investigated the influence of immune inflammation indicators on treatment outcome of anal ca...

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Veröffentlicht in:Cancer management and research 2019-01, Vol.11, p.3631-3642
Hauptverfasser: Casadei-Gardini, Andrea, Montagnani, Francesco, Casadei, Chiara, Arcadipane, Francesca, Andrikou, Kalliopi, Aloi, Deborah, Prete, Alessandra Anna, Zampino, Maria Giulia, Argentiero, Antonella, Pugliese, Giuseppe, Martini, Stefania, Iorio, Giuseppe Carlo, Scartozzi, Mario, Mistrangelo, Massimiliano, Fornaro, Lorenzo, Cassoni, Paola, Marisi, Giorgia, Dell'Acqua, Veronica, Ravenda, Paola Simona, Lonardi, Sara, Silvestris, Nicola, De Bari, Berardino, Ricardi, Umberto, Cascinu, Stefano, Franco, Pierfrancesco
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Sprache:eng
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Zusammenfassung:In anal cancer, there are no markers nor other laboratory indexes that can predict prognosis and guide clinical practice for patients treated with concurrent chemoradiation. In this study, we retrospectively investigated the influence of immune inflammation indicators on treatment outcome of anal cancer patients undergoing concurrent chemoradiotherapy. All patients had a histologically proven diagnosis of squamous cell carcinoma of the anal canal/margin treated with chemoradiotherapy according to the Nigro's regimen. Impact on prognosis of pre-treatment systemic index of inflammation (SII) (platelet x neutrophil/lymphocyte), neutrophil-lymphocyte ratio (NLR) and platelet-lymphocyte ratio (PLR) were analyzed. A total of 161 consecutive patients were available for the analysis. Response to treatment was the single most important factor for progression-free survival (PFS) and overall survival (OS). At univariate analysis, higher SII level was significantly correlated to lower PFS (
ISSN:1179-1322
1179-1322
DOI:10.2147/CMAR.S197349