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The Systemic Inflammatory Response Identifies Patients with Adverse Clinical Outcome from Immunotherapy in Hepatocellular Carcinoma

Authors :
Ambreen Muhammed
Claudia Angela Maria Fulgenzi
Sirish Dharmapuri
Matthias Pinter
Lorenz Balcar
Bernhard Scheiner
Thomas U. Marron
Tomi Jun
Anwaar Saeed
Hannah Hildebrand
Mahvish Muzaffar
Musharraf Navaid
Abdul Rafeh Naqash
Anuhya Gampa
Umut Ozbek
Junk-Yi Lin
Ylenia Perone
Bruno Vincenzi
Marianna Silletta
Anjana Pillai
Yinghong Wang
Uqba Khan
Yi-Hsiang Huang
Dominik Bettinger
Yehia I. Abugabal
Ahmed Kaseb
Tiziana Pressiani
Nicola Personeni
Lorenza Rimassa
Naoshi Nishida
Luca Di Tommaso
Masatoshi Kudo
Arndt Vogel
Francesco A. Mauri
Alessio Cortellini
Rohini Sharma
Antonio D’Alessio
Celina Ang
David J. Pinato
Source :
Cancers, Vol 14, Iss 186, p 186 (2022), Web of Science, Cancers, Cancers; Volume 14; Issue 1; Pages: 186
Publication Year :
2022
Publisher :
MDPI AG, 2022.

Abstract

Simple Summary The investigation of predictive and prognostic markers is pivotal in patients affected by hepatocellular carcinoma treated with immune-checkpoint-inhibitors. Inflammation has a central role in hepatocellular carcinoma development and progression; however, its role in influencing outcomes in the context of immunotherapy has not been fully elucidated yet. In the following study, we investigated the prognostic role of bloods derived inflammatory markers and we found that they predict survival and response of patients treated with immunotherapy for advanced hepatocellular carcinoma. Abstract Systemic inflammation is a hallmark of cancer, and it has a pivotal role in hepatocellular carcinoma (HCC) development and progression. We conducted a retrospective study including 362 patients receiving immune check-point inhibitors (ICIs) across three continents, evaluating the influence of neutrophiles to lymphocytes ratio (NLR), platelets to lymphocytes ratio (PLR), and prognostic nutritional index (PNI) on overall (OS), progression free survival (PFS), and radiologic responses. In our 362 patients treated with immunotherapy, median OS and PFS were 9 and 3.5 months, respectively. Amongst tested inflammatory biomarkers, patients with NLR ≥ 5 had shorter OS (7.7 vs. 17.6 months, p < 0.0001), PFS (2.1 vs. 3.8 months, p = 0.025), and lower objective response rate (ORR) (12% vs. 22%, p = 0.034); similarly, patients with PLR ≥ 300 reported shorter OS (6.4 vs. 16.5 months, p < 0.0001) and PFS (1.8 vs. 3.7 months, p = 0.0006). NLR emerged as independent prognostic factors for OS in univariate and multivariate analysis (HR 1.95, 95%CI 1.45–2.64, p < 0.001; HR 1.73, 95%CI 1.23–2.42, p = 0.002) and PLR remained an independent prognostic factor for both OS and PFS in multivariate analysis (HR 1.60, 95%CI 1.6–2.40, p = 0.020; HR 1.99, 95%CI 1.11–3.49, p = 0.021). Systemic inflammation measured by NLR and PLR is an independent negative prognostic factor in HCC patients undergoing ICI therapy. Further studies are required to understand the biological mechanisms underlying this association and to investigate the predictive significance of circulating inflammatory biomarkers in HCC patients treated with ICIs.

Details

Language :
English
ISSN :
20726694
Volume :
14
Issue :
186
Database :
OpenAIRE
Journal :
Cancers
Accession number :
edsair.doi.dedup.....e2a40995ea7cfdfcb95cba3bfac46b8a