University of Washington Medical Center Seattle, WA
Elizabeth Tower, MD1, Kevin Ng, MSc2, Tengda Lin, MPH, MA3, Kelly Santuci, BS4, Cornelia M. Ulrich, MS, PhD4, Adetunji Toriola, MD, PhD5, Ted Gooley, PhD2, Christopher I. Li, MD, PhD2, David Shibata, MD6, Jennifer Ose, MSc, PhD3, Doratha Byrd, PhD, MPH7, Jane C. Figueiredo, PhD8, Sheetal Hardikar, MBBS, PhD, MPH4, Biljana Gigic, PhD9, Caroline Himbert, PhD3, Christy Warby, BA3, William M.. Grady, MD2 1University of Washington Medical Center, Seattle, WA; 2Fred Hutchinson Cancer Center, Seattle, WA; 3University of Utah, Salt Lake City, UT; 4Huntsman Cancer Institute, Salt Lake City, UT; 5Washington University School of Medicine in St. Louis, St. Louis, MO; 6University of Tennessee Health Science Center, Memphis, TN; 7Moffitt Cancer Center, Tampa, FL; 8Cedars-Sinai Medical Center, Los Angeles, CA; 9Heidelberg University Hospital, Heidelberg, Baden-Wurttemberg, Germany
Introduction: Colorectal cancer (CRC) is a significant cause of morbidity and mortality worldwide. Early-onset colorectal cancer (eoCRC) has an increasing incidence in comparison to later-onset colorectal cancer (loCRC). Inflammation has emerged as a potential contributing factor to CRC, particularly eoCRC. This study examines objective measurements of a comprehensive panel of established circulating pro-inflammatory markers to assess the correlation between these markers’ levels and age at CRC diagnosis.
Methods: A cohort of 744 patients was analyzed, 143 (19.2%) diagnosed with CRC before age 50 (eoCRC) and 601 (80.8%) diagnosed at age 50 or older (loCRC). Eleven biomarkers were examined: CRP, IL6, IL8, SAA, TNFa, VEGFA, VEGFD, sICAM1, sVCAM1, MCP1, and SDF1a. Linear regression models, both simple and multiple, were employed to assess associations between mean biomarker levels and age at diagnosis, adjusting for potential confounders, consisting of smoking status, tumor stage, and BMI.
Results: No statistical difference between eoCRC and loCRC patients was observed in CRP, IL-6, IL-8, SAA, sICAM1, MCP-1, and SDF1a levels (p > 0.05). No significant correlation was identified between these markers and age of diagnosis. TNFa demonstrated a significant positive correlation with age of diagnosis (p< 0.001), indicating higher levels with older age. However, there was no significant difference when comparing eoCRC and loCRC directly. Significant differences were found for VEGFA, VEGFD, and sVCAM1 with higher mean levels in the loCRC group in both simple (p=0.02, p< 0.001, p=0.001) and multiple regression (p=0.045, p< 0.001, p=0.002).
Discussion: While no significant association was found between age at diagnosis and certain pro-inflammatory biomarkers, significant differences were observed for VEGFA, VEGFD, and sVCAM1. These findings suggest age-related differences may exist more prominently in angiogenesis related pathways in CRC patients, specifically increasing with age. This may be consistent with prior findings that VEGF levels correlate with poorer prognosis and risk of advanced tumor stage and metastasis in CRC patients. There is also evidence that CRC patients with elevated VEGF levels have shorter survival and higher chemotherapy resistance vs those with lower levels. Further research and analysis is warranted to investigate the prognostic value of VEGF in eoCRC, to better understand the treatment and clinical outcome implications in this specific and growing patient population.
Note: The table for this abstract can be viewed in the ePoster Gallery section of the ACG 2024 ePoster Site or in The American Journal of Gastroenterology's abstract supplement issue, both of which will be available starting October 27, 2024.
Disclosures:
Elizabeth Tower indicated no relevant financial relationships.
Kevin Ng indicated no relevant financial relationships.
Tengda Lin indicated no relevant financial relationships.
Kelly Santuci indicated no relevant financial relationships.
Cornelia M. Ulrich indicated no relevant financial relationships.
Adetunji Toriola indicated no relevant financial relationships.
Ted Gooley indicated no relevant financial relationships.
Christopher Li indicated no relevant financial relationships.
David Shibata indicated no relevant financial relationships.
Jennifer Ose indicated no relevant financial relationships.
Doratha Byrd indicated no relevant financial relationships.
Jane Figueiredo indicated no relevant financial relationships.
Sheetal Hardikar indicated no relevant financial relationships.
Biljana Gigic indicated no relevant financial relationships.
Caroline Himbert indicated no relevant financial relationships.
Christy Warby indicated no relevant financial relationships.
Elizabeth Tower, MD1, Kevin Ng, MSc2, Tengda Lin, MPH, MA3, Kelly Santuci, BS4, Cornelia M. Ulrich, MS, PhD4, Adetunji Toriola, MD, PhD5, Ted Gooley, PhD2, Christopher I. Li, MD, PhD2, David Shibata, MD6, Jennifer Ose, MSc, PhD3, Doratha Byrd, PhD, MPH7, Jane C. Figueiredo, PhD8, Sheetal Hardikar, MBBS, PhD, MPH4, Biljana Gigic, PhD9, Caroline Himbert, PhD3, Christy Warby, BA3, William M.. Grady, MD2. P2142 - Comparison of Pro-Inflammatory Circulating Biomarkers Between Early vs Later Onset Colorectal Cancer: Results From the ColoCare Study, ACG 2024 Annual Scientific Meeting Abstracts. Philadelphia, PA: American College of Gastroenterology.