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 session 18

961P - Blood circulating Galectin-3 is a prognostic biomarker in hepatocellular carcinoma

Date

21 Oct 2023

Session

Poster session 18

Topics

Tumour Site

Hepatobiliary Cancers

Presenters

Shadi Chamseddine

Citation

Annals of Oncology (2023) 34 (suppl_2): S594-S618. 10.1016/S0923-7534(23)01939-7

Authors

S. Chamseddine1, A. Kaseb2

Author affiliations

  • 1 Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center - Main Building, 77030 - Houston/US
  • 2 Gi Medical Oncology Dept., The University of Texas M. D. Anderson Cancer Center, 77030 - Houston/US

Resources

Login to get immediate access to this content.

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

Abstract 961P

Background

Galectin-3 plays critical roles in the adhesion, proliferation, and differentiation of tumor cells. Recent data has suggested that galectin-3 plays a role in the development of hepatocellular carcinoma (HCC), however, its prognostic value has not been validated. The aim of our study was to evaluate the clinical and prognostic value of galectin-3 in HCC patients.

Methods

We prospectively enrolled and collected clinicopathologic data and serum samples from 767 HCC patients between 2001 and 2014 at The University of Texas MD Anderson Cancer Center. The cut-off value for low versus high galectin-3 levels was established using ROC curve analysis. The Kaplan-Meier method was used to estimate overall survival (OS) distributions.

Results

The median OS in this cohort was 14.2 months (95% confidence interval [CI]: 12, 16.1 months). OS was significantly associated with clinicopathologic features, including tumor-node-metastasis (TNM) staging (p<0.001), Child-Pugh Score (CPS) (p<0.001), cirrhosis (p<0.001), metastasis (p<0.001), and alpha-fetoprotein (AFP) level (p<0.001). At the time of analysis, the one-year OS rate was 45% (95% CI: 0.4, 0.51) among patients with high galectin-3 levels, and 59% (95% CI: 0.54, 0.63) among patients with low galectin-3 levels. OS was significantly inferior in patients with high galectin-3 levels compared to patients with lower galectin-3 levels (median OS: 10.12 vs 16.49 months; p=0.0022). Higher galectin-3 levels were significantly associated with a higher risk of death (HR =1.29, 95% CI: 1.1, 1.53). Comparison between low (n = 464 patients) and high (n = 302 patients) galectin-3 levels showed that mean serum galectin-3 levels were significantly higher in HCC patients with HCV (p=0.0001), viral-induced hepatitis (p=0.0002), higher Child-Pugh Score (CPS) (p=0.0009), and higher Cancer of the Liver Italian Program (CLIP) score (p=0.0015).

Conclusions

In conclusion, our study shows that serum galectin-3 level is a valid prognostic biomarker candidate and a potential target for therapy in HCC.

Clinical trial identification

Editorial acknowledgement

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.