PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 34453221-0 2021 Lenvatinib plus TACE with or without pembrolizumab for the treatment of initially unresectable hepatocellular carcinoma harbouring PD-L1 expression: a retrospective study. lenvatinib 0-10 CD274 molecule Homo sapiens 131-136 34453221-1 2021 PURPOSE: The aim of this retrospective study was to compare the clinical outcomes of pembrolizumab-lenvatinib-transarterial chemoembolization (TACE) versus lenvatinib-TACE sequential therapy in selected populations of Chinese patients with initially unresectable hepatocellular carcinoma (uHCC) harbouring programmed cell death ligand-1 (PD-L1) expression. lenvatinib 99-109 CD274 molecule Homo sapiens 306-336 34453221-1 2021 PURPOSE: The aim of this retrospective study was to compare the clinical outcomes of pembrolizumab-lenvatinib-transarterial chemoembolization (TACE) versus lenvatinib-TACE sequential therapy in selected populations of Chinese patients with initially unresectable hepatocellular carcinoma (uHCC) harbouring programmed cell death ligand-1 (PD-L1) expression. lenvatinib 99-109 CD274 molecule Homo sapiens 338-343 34453221-1 2021 PURPOSE: The aim of this retrospective study was to compare the clinical outcomes of pembrolizumab-lenvatinib-transarterial chemoembolization (TACE) versus lenvatinib-TACE sequential therapy in selected populations of Chinese patients with initially unresectable hepatocellular carcinoma (uHCC) harbouring programmed cell death ligand-1 (PD-L1) expression. lenvatinib 156-166 CD274 molecule Homo sapiens 306-336 34453221-1 2021 PURPOSE: The aim of this retrospective study was to compare the clinical outcomes of pembrolizumab-lenvatinib-transarterial chemoembolization (TACE) versus lenvatinib-TACE sequential therapy in selected populations of Chinese patients with initially unresectable hepatocellular carcinoma (uHCC) harbouring programmed cell death ligand-1 (PD-L1) expression. lenvatinib 156-166 CD274 molecule Homo sapiens 338-343 34036623-3 2021 APPROACH & RESULTS: First, in patients with HCC, lenvatinib-treated recurrent tumors had lower programmed death ligand 1 (PD-L1) expression and regulatory T cell (Treg) infiltration compared with matched primary tumors. lenvatinib 49-59 CD274 molecule Homo sapiens 95-120 34036623-10 2021 CONCLUSIONS: Lenvatinib reduced tumor PD-L1 level and Treg differentiation to improve anti-PD-1 efficacy by blocking FGFR4. lenvatinib 13-23 CD274 molecule Homo sapiens 38-43 34168004-0 2021 Tumor-derived lactate inhibit the efficacy of lenvatinib through regulating PD-L1 expression on neutrophil in hepatocellular carcinoma. lenvatinib 46-56 CD274 molecule Homo sapiens 76-81 34168004-3 2021 In this study, we elucidate the stimulators of PD-L1+ neutrophils in tumor microenvironment (TME) and explore the optimal combination to enhance the effect of lenvatinib by inhibiting PD-L1+ neutrophils in hepatocellular carcinoma. lenvatinib 159-169 CD274 molecule Homo sapiens 47-52 34168004-3 2021 In this study, we elucidate the stimulators of PD-L1+ neutrophils in tumor microenvironment (TME) and explore the optimal combination to enhance the effect of lenvatinib by inhibiting PD-L1+ neutrophils in hepatocellular carcinoma. lenvatinib 159-169 CD274 molecule Homo sapiens 184-189 34036623-3 2021 APPROACH & RESULTS: First, in patients with HCC, lenvatinib-treated recurrent tumors had lower programmed death ligand 1 (PD-L1) expression and regulatory T cell (Treg) infiltration compared with matched primary tumors. lenvatinib 49-59 CD274 molecule Homo sapiens 122-127 32087304-11 2020 Knock down of HDACs1/2/3 prevented the lenvatinib and entinostat combination from regulating PD-L1 and MHCA expression. lenvatinib 39-49 CD274 molecule Homo sapiens 93-98 33757737-12 2021 In patients with >=1% PD-L1 expression, the highest likelihood of better PFS was associated with lenvatinib plus pembrolizumab and nivolumab plus ipilimumab. lenvatinib 97-107 CD274 molecule Homo sapiens 22-27 32647635-16 2020 Finally, lenvatinib inhibited PD-L1 expression on human umbilical vein endothelial cells, which improved the function of T cells. lenvatinib 9-19 CD274 molecule Homo sapiens 30-35