1. Early age of onset is an independent predictor for worse disease-free survival in sporadic rectal cancer patients. A comparative analysis of 980 consecutive patients
- Author
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José Perea, L. Poliani, Annalisa Maroli, Caterina Foppa, A. Malesci, Marco Montorsi, Antonino Spinelli, Sara Tamburello, Luigi Laghi, and Michele Carvello
- Subjects
medicine.medical_specialty ,Colorectal cancer ,Gene mutation ,medicine.disease_cause ,Gastroenterology ,Disease-Free Survival ,Internal medicine ,medicine ,Humans ,Progression-free survival ,Stage (cooking) ,Family history ,Age of Onset ,Neoplasm Staging ,Retrospective Studies ,business.industry ,Rectal Neoplasms ,Microsatellite instability ,General Medicine ,medicine.disease ,Prognosis ,Progression-Free Survival ,Oncology ,Surgery ,KRAS ,Age of onset ,Neoplasm Recurrence, Local ,business - Abstract
BACKGROUND while interest on early-onset colorectal cancer (age ≤49) is on the rise, studies on early-onset rectal cancer (EORC) are limited. The aim of this study was to compare predictors for disease progression/recurrence between sporadic EORC and late-onset RC patients (LORC). METHODS 163 EORC and 830 LORC operated between January 1st, 2010 and April 30th, 2021 at a tertiary center were included. Demographics, tumor characteristics, microsatellite status, gene mutations (KRAS, BRAF, NRAS, PI3Kca) and oncologic outcomes were compared. A Cox proportional hazards regression analysis was performed to ascertain the effect of variables on recurrence/progression and death. Recurrence/Progression free survival (R/PFS) and cancer specific survival (CSS) were analyzed by the Kaplan-Meier estimator. RESULTS Mean age of EORC was 42.16, (46% aged 45-49). A majority of EORC patients had a family history for CRC (p = 0.01) and underwent total neoadjuvant treatment (p = 0.01). EORC patients showed a higher rate of low-grade tumor differentiation (p
- Published
- 2021