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Progress of targeted and immunotherapy for hepatocellular carcinoma and the application of next-generation sequencing
Fan Yang 1 , Kaige Deng 1 , Haoran Zheng 1 , Zhenting Liu 1 , Yongchang Zheng 2
Affiliations
Affiliations
1
Department of liver surgery, Peking Union Medical College Hospital, Beijing, China.
2
Department of liver surgery, Peking Union Medical College Hospital, Beijing, China. Electronic address: [email protected].
PMID: 35093601 DOI: 10.1016/j.aohep.2022.100677
Abstract
Hepatocellular carcinoma (HCC), leading cancer worldwide, has a high degree of genetic heterogeneity; next-generation sequencing (NGS) technology has contributed significantly to the discovery of driving genes as well as high-frequency mutations in HCC. The detection of gene alterations may allow us to predict prognosis and adverse drug reactions for individuals, paving the way for personalized medicine in HCC patients. In this review, we summarized the common systemic therapy regimens for HCC and the predictive efficacy of genetic biomarkers on the prognosis of patients under these treatments. Finally, we put forward a future perspective on the potential of NGS technology for the guidance of targeted therapy and immunotherapy in HCC.
Keywords: Abbreviations: HCC: Hepatocellular carcinoma; CCL5: Chemokine ligand 5; CRLM: Colorectal liver metastases; CTLA-4: Cytotoxic T-lymphocyte-associated protein 4; DCR: Disease control rates; EGFR: Epidermal growth factor receptor; FGFR: Fibroblast growth factor receptor; FISH: Fluorescence in situ hybridization; HBV: Hepatitis B virus; HRR: Homologous recombination repair; Hepatocellular carcinoma; ICI: Immune checkpoint inhibitors; IFN: Interferon; IHC: Immunohistochemistry; IPM: Immune prognosis model; NCCN: National Comprehensive Cancer Network; NGS: Next-generation sequencing; NSCLC: Non-small cell lung cancer; ORR: Objective effective rate; OS: Overall survival; PCR: Polymerase chain reaction; PD-1: Programmed death 1; PD-L1: Programmed death ligand 1; PDGFR: Platelet-derived growth factor receptor; PFS: Progression-free survival time; PTK: Protein tyrosine kinases; RT-PCR: Reverse transcription-polymerase chain reaction; RTK: Receptor tyrosine protein kinase; TCGA: The Cancer Genome Atlas; TKI: Tyrosine kinase inhibitor; TRM: Resident memory T cells; TTP: Time to progress; Treg: Regulatory T cells; VEGFR: Vascular endothelial growth factor receptor; WGS: Whole-genome sequencing; biomarker; gene detection; immunotherapy; mOS: Median overall survival; mPCR: Multiplex Polymerase Chain Reaction; precision medicine; targeted therapy; uHCC: unresectable Hepatocellular carcinoma.
Copyright © 2022. Published by Elsevier España, S.L.U. |
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