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Prognostic Differences Between Early-Onset and Late-Onset Colorectal Cancer
Vlad Alexandru Ionescu1,2, Gina Gheorghe1,2, Ioana-Alexandra Baban3
1Faculty of Medicine, University of Medicine and Pharmacy Carol Davila Bucharest, 050474 Bucharest, Romania.
Early-onset colorectal cancer (EO-CRC) shows distinct aggressive features compared to late-onset CRC (LO-CRC). EO-CRC is linked to specific tumor subtypes, HER2 positivity, and lifestyle factors, necessitating tailored screening and treatment.
Area of Science:
- Oncology
- Gastroenterology
- Public Health
Background:
- Early-onset colorectal cancer (EO-CRC) incidence is rising, posing a significant public health challenge.
- EO-CRC is often associated with a poorer prognosis compared to late-onset colorectal cancer (LO-CRC).
- Understanding the distinct characteristics of EO-CRC is crucial for improving patient outcomes.
Purpose of the Study:
- To identify epidemiological, clinical, and paraclinical factors contributing to the aggressive nature of EO-CRC.
- To compare the characteristics of EO-CRC with those of LO-CRC.
Main Methods:
- Retrospective study of 204 colorectal cancer (CRC) patients over two years.
- Patients were categorized into EO-CRC and LO-CRC subgroups.
- Statistical analysis was performed using IBM SPSS Statistics, Version 29.0.
Main Results:
- EO-CRC accounted for 11.3% of cases and showed a trend towards more distal tumors and stenotic appearance.
- EO-CRC patients had a higher incidence of mucinous histology (34.8% vs. 14.4%) and poorly differentiated tumors (39.1% vs. 14.5%).
- Increased HER2 positivity (p=0.002) and reduced CDX2 positivity (p=0.012) were observed in EO-CRC, alongside higher prevalence of smoking and hypertension.
Conclusions:
- EO-CRC patients exhibit unique histopathological and molecular profiles, including mucinous subtype, poor differentiation, and altered HER2/CDX2 expression, contributing to aggressive disease.
- Lifestyle factors like smoking and hypertension are more common in EO-CRC patients.
- Findings support the need for tailored screening and personalized treatment strategies for younger CRC patients.
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