High serum IL-6 correlates with reduced clinical benefit of atezolizumab and bevacizumab in unresectable hepatocellular carcinoma.

JHEP reports : innovation in hepatology(2023)

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摘要
Although patients with hepatocellular carcinoma who respond to treatment with atezolizumab and bevacizumab exhibit favourable clinical outcomes, a fraction of these still experience primary resistance. We found that high baseline serum levels of IL-6 correlate with poor clinical outcomes and impaired T-cell response in patients with hepatocellular carcinoma treated with atezolizumab and bevacizumab.
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AFP, alpha-foetoprotein,Ate/Bev, atezolizumab and bevacizumab,Atezolizumab,BCLC, Barcelona Clinic Liver Cancer,Bevacizumab,CB6m, clinical benefit 6 months,CONSORT, Consolidated Standards of Reporting Trials,CR, complete response,CRAFITY, C-reactive protein and AFP in immunotherapy,CTLA-4, cytotoxic T-lymphocyte-associated protein 4,DC, dendritic cell,ECOG, Eastern Cooperative Oncology Group,FFPE, formalin-fixed paraffin-embedded,HCC, hepatocellular carcinoma,HR, hazard ratio,Hepatocellular carcinoma,IFN-γ, interferon-γ,IL-6,Immunotherapy,MDSC, myeloid-derived suppressor cell,MSI, microsatellite instability,MVI, macrovascular invasion,ORR, objective response rate,OS, overall survival,PBMC, peripheral blood mononuclear cell,PD, progressive disease,PD-1, programmed-death-1,PD-L1, programmed-death ligand-1,PFS, progression-free survival,PR, partial response,RECIST, Response Evaluation Criteria in Solid Tumours,SD, stable disease,TME, tumour microenvironment,TNF-α, tumour necrosis factor-α,VEGF, vascular endothelial growth factor
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