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T-Cell Dynamics Predicts Prognosis of Patients with Hepatocellular Carcinoma Receiving Atezolizumab Plus Bevacizumab

Authors
 Hye Won Lee  ;  Suebin Park  ;  Hye Jung Park  ;  Kyung Joo Cho  ;  Do Young Kim  ;  Byungjin Hwang  ;  Jun Yong Park 
Citation
 INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, Vol.25(20) : 10958, 2024-10 
Journal Title
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
ISSN
 1661-6596 
Issue Date
2024-10
MeSH
Aged ; Antibodies, Monoclonal, Humanized* / administration & dosage ; Antibodies, Monoclonal, Humanized* / therapeutic use ; Antineoplastic Combined Chemotherapy Protocols* / therapeutic use ; Bevacizumab* / therapeutic use ; CD8-Positive T-Lymphocytes / immunology ; Carcinoma, Hepatocellular* / drug therapy ; Carcinoma, Hepatocellular* / immunology ; Carcinoma, Hepatocellular* / mortality ; Carcinoma, Hepatocellular* / pathology ; Female ; Humans ; Liver Neoplasms* / drug therapy ; Liver Neoplasms* / immunology ; Liver Neoplasms* / mortality ; Liver Neoplasms* / pathology ; Male ; Middle Aged ; Prognosis ; T-Lymphocytes / drug effects ; T-Lymphocytes / immunology ; T-Lymphocytes / metabolism
Keywords
atezolizumab ; bevacizumab ; hepatocellular carcinoma ; immune dynamics ; prognostic markers
Abstract
Atezolizumab and bevacizumab show promise for treating hepatocellular carcinoma (HCC), but identifying responsive patients remains challenging, due to tumor heterogeneity. This study explores immune dynamics following this combination therapy. Between 2020 and 2023, 29 patients with advanced HCC who received atezolizumab plus bevacizumab at Severance Hospital, Seoul, were enrolled in this study. Peripheral blood mononuclear cells were analyzed using flow cytometry and statistical methods to assess immune alterations and identify biomarkers. Baseline characteristics showed a diverse HCC cohort with a mean age of 64 years and 82.8% male predominance. Absence of extrahepatic metastasis was associated with better overall survival. Immune responses revealed distinct CD4+ T-cell phenotypes between the 'partial response (PR) + stable disease (SD)' and 'progressive disease (PD)' groups, with an overall increase in CD8+ T-cell phenotypes. Patients with higher frequencies of CD8+PD-1+Ki-67+ T cells experienced significantly improved overall survival, while those with lower frequencies of CD4+Foxp3+PD-1+LAG3+ T cells also had notable survival benefits. These findings enhance the overall understanding of immune responses to this combination therapy, facilitating improved patient stratification and personalized therapeutic approaches for HCC.
Files in This Item:
T202406852.pdf Download
DOI
10.3390/ijms252010958
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Yonsei Biomedical Research Center (연세의생명연구원) > 1. Journal Papers
1. College of Medicine (의과대학) > BioMedical Science Institute (의생명과학부) > 1. Journal Papers
Yonsei Authors
Kim, Do Young(김도영)
Park, Jun Yong(박준용) ORCID logo https://orcid.org/0000-0001-6324-2224
Park, Hye Jung(박혜정) ORCID logo https://orcid.org/0000-0002-1862-1003
Lee, Hye Won(이혜원) ORCID logo https://orcid.org/0000-0002-3552-3560
Cho, Kyuong Joo(조경주)
Hwang, Byungjin(황병진)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/206532
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