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

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dc.contributor.author김도영-
dc.contributor.author박준용-
dc.contributor.author박혜정-
dc.contributor.author이혜원-
dc.contributor.author조경주-
dc.contributor.author황병진-
dc.date.accessioned2025-07-09T08:37:17Z-
dc.date.available2025-07-09T08:37:17Z-
dc.date.issued2024-10-
dc.identifier.issn1661-6596-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/206532-
dc.description.abstractAtezolizumab 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.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherMDPI-
dc.relation.isPartOfINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAged-
dc.subject.MESHAntibodies, Monoclonal, Humanized* / administration & dosage-
dc.subject.MESHAntibodies, Monoclonal, Humanized* / therapeutic use-
dc.subject.MESHAntineoplastic Combined Chemotherapy Protocols* / therapeutic use-
dc.subject.MESHBevacizumab* / therapeutic use-
dc.subject.MESHCD8-Positive T-Lymphocytes / immunology-
dc.subject.MESHCarcinoma, Hepatocellular* / drug therapy-
dc.subject.MESHCarcinoma, Hepatocellular* / immunology-
dc.subject.MESHCarcinoma, Hepatocellular* / mortality-
dc.subject.MESHCarcinoma, Hepatocellular* / pathology-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHLiver Neoplasms* / drug therapy-
dc.subject.MESHLiver Neoplasms* / immunology-
dc.subject.MESHLiver Neoplasms* / mortality-
dc.subject.MESHLiver Neoplasms* / pathology-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHPrognosis-
dc.subject.MESHT-Lymphocytes / drug effects-
dc.subject.MESHT-Lymphocytes / immunology-
dc.subject.MESHT-Lymphocytes / metabolism-
dc.titleT-Cell Dynamics Predicts Prognosis of Patients with Hepatocellular Carcinoma Receiving Atezolizumab Plus Bevacizumab-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorHye Won Lee-
dc.contributor.googleauthorSuebin Park-
dc.contributor.googleauthorHye Jung Park-
dc.contributor.googleauthorKyung Joo Cho-
dc.contributor.googleauthorDo Young Kim-
dc.contributor.googleauthorByungjin Hwang-
dc.contributor.googleauthorJun Yong Park-
dc.identifier.doi10.3390/ijms252010958-
dc.contributor.localIdA00385-
dc.contributor.localIdA01675-
dc.contributor.localIdA01769-
dc.contributor.localIdA03318-
dc.contributor.localIdA03804-
dc.contributor.localIdA06348-
dc.relation.journalcodeJ01133-
dc.identifier.eissn1422-0067-
dc.identifier.pmid39456740-
dc.subject.keywordatezolizumab-
dc.subject.keywordbevacizumab-
dc.subject.keywordhepatocellular carcinoma-
dc.subject.keywordimmune dynamics-
dc.subject.keywordprognostic markers-
dc.contributor.alternativeNameKim, Do Young-
dc.contributor.affiliatedAuthor김도영-
dc.contributor.affiliatedAuthor박준용-
dc.contributor.affiliatedAuthor박혜정-
dc.contributor.affiliatedAuthor이혜원-
dc.contributor.affiliatedAuthor조경주-
dc.contributor.affiliatedAuthor황병진-
dc.citation.volume25-
dc.citation.number20-
dc.citation.startPage10958-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, Vol.25(20) : 10958, 2024-10-
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

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