Evaluation of Prognostic Factors for Survival in Transverse Colon Cancer

Author:

Roberto MichelaORCID,Arrivi Giulia,Lo Bianco Francesca,Cascinu Stefano,Gelsomino Fabio,Caputo Francesco,Cerma Krisida,Ghidini MicheleORCID,Ratti Margherita,Pizzo Claudio,Ficorella Corrado,Parisi AlessandroORCID,Cortellini AlessioORCID,Urbano Federica,Calandrella Maria Letizia,Dell’Aquila Emanuela,Minelli Alessandro,Fulgenzi Claudia Angela MariaORCID,Gariazzo Ludovica,Montori AndreaORCID,Pilozzi Emanuela,Di Girolamo Marco,Marchetti Paolo,Mazzuca Federica

Abstract

Background: Although most of the analyses included transverse colon cancers (TCC) among right colon cancer (RCC), it is not completely clear if they present total similarities with RCC or if they have their specific features. Therefore, we present an observational study to evaluate clinicopathological characteristics and survival data of patients with TCC. Methods: We retrospectively reviewed 450 RCC, of whom 97 stages I–IV TCC were included in this multicenter study; clinicopathological and molecular parameters were analyzed to identify prognostic factors for disease-free survival (DFS) and overall survival (OS). Results: Most of TCC cases were male (61%), with ≤70 years old (62%), and good performance status (ECOG PS 0, 68%). According to WHO classification, 41 (49%) and 40 (48%) tumors were classified as well to moderate and poorly/undifferentiated respectively, regardless of mucinous component (30%). About molecular data, 8 (26%), 45 (63%), and 14 (24%) were MSI-H, KRAS wild-type, and BRAF V600E mutant, respectively. With a median follow-up of 34 months, there were 29 and 50 disease recurrences and deaths respectively. Charlson comorbidity index ≥5 was a significant prognostic factor for DFS (HR = 7.67, 95% CI 2.27–25.92). Colon obstruction/perforation (HR = 2.65, 95% CI 1.01–7.01), and BRAF mutant (HR = 3.03, 95% CI 0.97–9.50) cases showed a worst, despite not statistically significant, DFS. Whereas for OS, at the multivariate model, only tumor grade differentiation (HR = 5.26, 95% CI 1.98–14.01) and BRAF mutation status (3.71, 95% CI 1.07–12.89) were independent prognostic factors. Conclusions: Poorly/undifferentiated tumor grade and BRAF V600E mutation are independent prognostic factors for OS in TCC. Further prospective clinical trials are needed to better define TCC treatment in order to improve patient outcome.

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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