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The Impact of Surgical Resection in Early Onset Colorectal Cancer Patients With Liver Limited Disease

Year: 2026
Type: article
Study design: Observational Study
Abstract: Background Recent studies have shown an increased incidence of early-onset CRC (EO-CRC), particularly in advanced stages and with metastatic disease. Our study aimed to evaluate the role of metastasectomies related to the clinical and molecular characteristics of EO-CRC patients with liver metastases compared to average-onset CRC (AO-CRC) patients. Methods We retrospectively collected data from 1123 stage IV colorectal cancers, including 782 with liver metastases, from 5 different Italian institutions. The main objective of the study was to compare the overall survival of liver metastatic EO-CRC and AO-CRC patients who underwent metastasectomy versus those who were not resected. Results Liver resected EO-CRCs patients showed a statistically significant lower mOS than liver resected AO-CRCs (44.0 vs 64.0 months, p < 0.0001 ). mPFS was also statistically significant lower in EO-CRCs (13.0 vs 17.0, p < 0.0001 ). Same outcomes were found in RAS mut subgroup (37.0 vs 52.0 months, p < 0.0001) and in RAS/BRAF wild-type subgroup (50.0 vs 81.0 months, p < 0.0001). EO-CRC patients showed a higher prevalence of TP53 alterations (56.2%) and a lower of APC mutation (29.9%). EO-CRCs presented a higher frequency of ARID1A (4.4%) and CTNNB1 (3.0%) alterations. Conclusion The results indicate a worse overall prognosis for EO-CRC patients undergoing metastasectomy compared to average-onset patients. This outcome appears to occur independently of the molecular status. These observations could have a considerable impact on clinical practice and research. Micro Abstract In a multicenter cohort of 1209 metastatic CRC patients , early-onset colorectal cancer (≤50 years) showed consistently inferior outcomes after liver metastasectomy. Among the 417 resected cases, EO-CRC had markedly shorter OS (44 vs 64 months) and PFS (13 vs 17 months) compared with older patients. This survival gap persisted across RAS-mutated and RAS/BRAF wild-type subgroups, suggesting a distinct and more aggressive EO-CRC phenotype.
Language: English
Subfield: Oncology
Field: Medicine
Open Access status: hybrid
Estimated APC paid: $3,690
OpenAlex ID: W7129448191
FWCI:
Cites: 29
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