The prognostic impact of RAS on overall survival following liver resection in early versus late-onset colorectal cancer patients

Alexandre A. Jácome, Timothy J. Vreeland, Benny Johnson, Yoshikuni Kawaguchi, Steven H. Wei, Y. Nancy You, Eduardo Vilar, Jean Nicolas Vauthey, Cathy Eng

Research output: Contribution to journalArticlepeer-review

17 Scopus citations

Abstract

Background: The impact of molecular aberrations on survival after resection of colorectal liver metastases (CLM) in patients with early-age-onset (EOCRC) versus late-age-onset colorectal cancer (LOCRC) is unknown. Methods: Patients who underwent liver resection for CLM with known RAS, BRAF and MSI status were retrospectively studied. The prognostic impact of RAS mutations by age was analysed with age as a categorical variable and a continuous variable. Results: The study included 573 patients, 192 with EOCRC and 381 with LOCRC. The younger the age of onset of CRC, the greater the negative impact on overall survival of RAS mutations in the LOCRC, EOCRC, and ≤40 years (hazard ratio (HR), 1.64 (95% confidence interval (CI), 1.23–2.20), 2.03 (95% CI, 1.30–3.17), and 2.97 (95% CI, 1.44–6.14), respectively. Age-specific mortality risk and linear regression analysis also demonstrated that RAS mutations had a greater impact on survival in EOCRC than in LOCRC (slope: −4.07, 95% CI −8.10 to 0.04, P = 0.047, R2 = 0.08). Conclusion: Among patients undergoing CLM resection, RAS mutations have a greater negative influence on survival in patients with EOCRC, more so in patients ≤40 years, than in patients with LOCRC and should be considered as a prognostic factor in multidisciplinary treatment planning.

Original languageEnglish (US)
Pages (from-to)797-804
Number of pages8
JournalBritish journal of cancer
Volume124
Issue number4
DOIs
StatePublished - Feb 16 2021

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

Fingerprint

Dive into the research topics of 'The prognostic impact of RAS on overall survival following liver resection in early versus late-onset colorectal cancer patients'. Together they form a unique fingerprint.

Cite this