Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

Poster Display session

368P - The role of pretreatment serum interleukin 6 in predicting short-term mortality in patients with advanced pancreatic cancer

Date

27 Jun 2024

Session

Poster Display session

Presenters

Dongwoo Cho

Citation

Annals of Oncology (2024) 35 (suppl_1): S119-S161. 10.1016/annonc/annonc1481

Authors

D. Cho1, J.Y. Park2, K. Shin3, T.H. Hong1, Y. Kim1, I. Kim4, M.A. Lee5, S.J. Park3

Author affiliations

  • 1 The Catholic University of Korea - Seoul St.Mary Hospital, Seoul/KR
  • 2 The Catholic University of Korea - College of Medicine, Seoul/KR
  • 3 The Catholic University of Korea - Seoul St. Mary's Hospital - Catholic Medical Center, Seoul/KR
  • 4 The Catholic University of Korea - College of Medicine - Songeui Medical Campus, Seoul/KR
  • 5 The Catholic University of Korea, Seoul/KR

Resources

Login to get immediate access to this content.

If you do not have an ESMO account, please create one for free.

Abstract 368P

Background

Pancreatic ductal adenocarcinoma (PDAC) is known for its aggressive behavior and poor outcomes. Elevated interleukin 6 (IL-6) levels, a pro-inflammatory cytokine, were observed in PDAC patients, correlating with increased disease severity. This research investigates the role of baseline serum IL-6 as a prognostic indicator in patients with advanced PDAC.

Methods

IL-6 and soluble IL-6 receptor α (sIL-6Rα) were derived from pre-treatment serum samples isolated using ELISA kit from 77 patients with advanced pancreatic cancer. The optimal cutoff value for 6-month survival regarding IL-6 and the IL-6:sIL-6Rα ratio was assessed using the receiver operating characteristic curve analysis. Kaplan-Meier analysis was performed to obtain median overall survival (mOS), and hazard ratio was estimated using a stratified Cox regression model.

Results

Higher serum IL-6 levels were significantly associated with poorly differentiated histology (p = 0.004), higher tumor burden (p = 0.025), and low baseline albumin level (p = 0.006). Based on each cutoff, the entire cohort was divided into groups of low IL-6 (49 patients) and high IL-6 (28 patients), or low IL-6:sIL-6Rα (43 patients) and high IL-6:sIL-6Rα (34 patients). At a median follow-up of 9.28 months, the mOS was 13.3 months in the low IL-6 group, compared with 3.63 months in the high IL-6 group (HR = 0.33; 95% CI, 0.18–0.60; p < 0.0001). Similarly, in the groups divided by the IL-6:sIL-6Rα ratio, the low group had a better OS outcome than the high group (HR = 0.32; 95% CI, 0.18–0.56; p < 0.0001). The median progression-free survival (PFS) was 9.12 months in the low IL-6 group compared with 2.07 months in the high IL-6 group (HR = 0.26; 95% CI, 0.12–0.58; p < 0.0001). A significant difference in PFS was also observed between the two groups divided according to the IL-6:sIL-6Rα ratio (HR = 0.32; 95% CI, 0.17–0.63; p < 0.0001). In the multivariate analysis for OS, IL-6 levels (HR = 2.31; 95% CI, 1.27–4.20; p = 0.006) were significantly associated with a worse prognosis, along with older age and a higher neutrophil to lymphocyte ratio.

Conclusions

The serum-derived IL-6 levels were associated with rapid disease progression and short-term mortality in patients with advanced pancreatic cancer.

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.