Clinical Impact of Serum CRP Levels on Advanced HCC Treated With Durvalumab and Tremelimumab: A Multicentre Study

Takeshi Hatanaka1, Yutaka Yata2, Atsushi Hiraoka3

  • 1Department of Gastroenterology, Gunma Saiseikai Maebashi Hospital, Maebashi, Japan.

Insights

Low C-reactive protein (CRP) levels predict better outcomes for advanced liver cancer patients treated with durvalumab and tremelimumab. Elevated CRP indicates a poorer prognosis, highlighting CRP as a key prognostic biomarker.

Area of Science:

  • Oncology
  • Immunotherapy
  • Biomarker Discovery

Background:

  • Advanced hepatocellular carcinoma (HCC) presents significant treatment challenges.
  • Durvalumab and tremelimumab (Dur/Tre) offer a therapeutic option for advanced HCC.
  • Identifying predictive biomarkers is crucial for optimizing treatment strategies.

Purpose of the Study:

  • To assess the therapeutic efficacy of Dur/Tre in advanced HCC.
  • To evaluate C-reactive protein (CRP) as a prognostic biomarker in this patient cohort.
  • To determine the association between pre-treatment CRP levels and patient outcomes.

Main Methods:

  • Retrospective multicentre study of 167 advanced HCC patients treated with Dur/Tre.
  • Patients categorized into low-CRP (<1 mg/dL) and high-CRP (≥1 mg/dL) groups.
  • Analysis of progression-free survival (PFS) and overall survival (OS) based on CRP levels.

Main Results:

  • The low-CRP group exhibited significantly longer PFS (3.6 months) and superior OS (1-year survival 64.7%) compared to the high-CRP group (PFS 2.4 months, OS 7.9 months).
  • Pre-treatment serum CRP level was identified as an independent predictive factor for both PFS and OS.
  • No significant differences in immune-related adverse events were observed between CRP groups.

Conclusions:

  • Serum CRP is a valuable prognostic biomarker for advanced HCC patients undergoing Dur/Tre therapy.
  • Lower CRP levels are associated with improved survival outcomes.
  • CRP may help predict treatment efficacy and guide clinical decision-making.
Abstract