Changes in Serum Interleukin-8 Levels Predict Response to Immune Checkpoint Inhibitors Immunotherapy in Unresectable Hepatocellular Carcinoma Patients
View abstract on PubMed
Summary
This summary is machine-generated.Early increases in serum interleukin-8 (IL-8) predict poor response to immune checkpoint inhibitors (ICIs) in liver cancer. An 8.1% rise in IL-8 indicates therapy futility and worse survival outcomes for hepatocellular carcinoma (HCC) patients.
Area Of Science
- Oncology
- Immunology
- Biomarker Discovery
Background
- Hepatocellular carcinoma (HCC) requires effective biomarkers to predict immune checkpoint inhibitor (ICI) therapy response.
- Current treatment strategies necessitate reliable indicators for personalized therapeutic decisions.
Purpose Of The Study
- To evaluate early changes in serum interleukin-8 (IL-8) as a predictive biomarker for ICI therapy efficacy in unresectable HCC.
- To determine the association between IL-8 dynamics and treatment outcomes, including overall survival (OS) and progression-free survival (PFS).
Main Methods
- Serum IL-8 levels were measured using ELISA in 80 unresectable HCC patients at baseline and 2-4 weeks post-ICI initiation.
- Statistical analyses were performed to correlate IL-8 changes with treatment response and survival data.
Main Results
- A significant increase in serum IL-8 levels was observed in patients with progressive disease (PD) before the second ICI dose (P < 0.001).
- Early IL-8 level changes strongly predicted ICI therapy response (P < 0.001).
- An increase >8.1% in serum IL-8 over baseline was identified as a threshold indicating ICI futility, predicting significantly shorter OS and PFS (P < 0.001) and serving as an independent prognosticator for worse survival.
Conclusions
- Early detection of serum IL-8 level changes (within 2-4 weeks) can predict ICI therapy response in HCC.
- An increase in serum IL-8 >8.1% signifies non-response to ICIs and predicts poorer OS and PFS, guiding clinical decision-making.

