Neutrophil-to-Lymphocyte and Platelet-to-Lymphocyte Ratios as Prognostic Biomarkers in Unresectable Hepatocellular Carcinoma Treated with Atezolizumab plus Bevacizumab

  • Yue Linda Wu
  • Claudia Angela Maria Fulgenzi
  • Antonio D'Alessio
  • Jaekyung Cheon
  • Naoshi Nishida
  • Anwaar Saeed
  • Brooke Wietharn
  • Antonella Cammarota
  • Tiziana Pressiani
  • Nicola Personeni
  • Matthias Pinter
  • Bernhard Scheiner
  • Lorenz Balcar
  • Yi-Hsiang Huang
  • Samuel Phen
  • Abdul Rafeh Naqash
  • Caterina Vivaldi
  • Francesca Salani
  • Gianluca Masi
  • Dominik Bettinger
  • Arndt Vogel
  • Martin Schönlein
  • Johann von Felden
  • Kornelius Schulze
  • Henning Wege
  • Peter R Galle
  • Masatoshi Kudo
  • Lorenza Rimassa
  • Amit G Singal
  • Rohini Sharma
  • Alessio Cortellini
  • Vincent E Gaillard
  • Hong Jae Chon
  • David J Pinato
  • Celina Ang

Abstract

Systemic inflammation is a key risk factor for hepatocellular carcinoma (HCC) progression and poor outcomes. Inflammatory markers such as the neutrophil-to-lymphocyte ratio (NLR) and platelet-to-lymphocyte ratio (PLR) may have prognostic value in HCC treated with standard of care atezolizumab plus bevacizumab (Atezo-Bev). We conducted a multicenter, international retrospective cohort study of patients with unresectable HCC treated with Atezo-Bev to assess the association of NLR and PLR with overall survival (OS), progression-free survival (PFS), and objective response rates. Patients with NLR ≥ 5 had a significantly shorter OS (9.38 vs. 16.79 months, p < 0.001) and PFS (4.90 vs. 7.58 months, p = 0.03) compared to patients with NLR < 5. NLR ≥ 5 was an independent prognosticator of worse OS (HR 2.01, 95% CI 1.22−3.56, p = 0.007) but not PFS. PLR ≥ 300 was also significantly associated with decreased OS (9.38 vs. 15.72 months, p = 0.007) and PFS (3.45 vs. 7.11 months, p = 0.04) compared to PLR < 300, but it was not an independent prognosticator of OS or PFS. NLR and PLR were not associated with objective response or disease control rates. NLR ≥ 5 independently prognosticated worse survival outcomes and is worthy of further study and validation.

Bibliographical data

Original languageEnglish
Article number5834
ISSN2072-6694
DOIs
Publication statusPublished - 26.11.2022
PubMed 36497316