Adoptive Cell Therapy in Hepatocellular Carcinoma: A Review of Clinical Trials
Özet
Hepatocellular carcinoma (HCC) is the most common type of primary liver cancer. Immune checkpoint inhibitors (ICIs) have become the new reference standard in first-line HCC treatment, replacing tyrosine kinase inhibitors (TKIs) such as sorafenib. Many clinical trials with different combinations are already in development to validate novel immunotherapies for the treatment of patients with HCC. Adoptive cell therapy (ACT), also known as cellular immunotherapy, with chimeric antigen receptors (CAR) or gene-modified T cells expressing novel T cell receptors (TCR) may represent a promising alternative approach to modify the immune system to recognize tumor cells with better clinical outcomes. In this review, we briefly discuss the overview of ACT as a promising treatment modality in HCC, along with recent updates of ongoing clinical trials. © 2023 by the authors.
Anahtar Kelimeler
Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Ozer, Muhammet | |
| dc.contributor.author | Goksu, Suleyman Yasin | |
| dc.contributor.author | Akagunduz, Baran | |
| dc.contributor.author | George, Andrew | |
| dc.contributor.author | Sahin, Ilyas | |
| dc.date.accessioned | 2026-10-18T20:27:19.763891325Z | |
| dc.date.available | 2026-10-18T20:27:19.763891325Z | |
| dc.date.issued | 2023 | |
| dc.description.abstract | Hepatocellular carcinoma (HCC) is the most common type of primary liver cancer. Immune checkpoint inhibitors (ICIs) have become the new reference standard in first-line HCC treatment, replacing tyrosine kinase inhibitors (TKIs) such as sorafenib. Many clinical trials with different combinations are already in development to validate novel immunotherapies for the treatment of patients with HCC. Adoptive cell therapy (ACT), also known as cellular immunotherapy, with chimeric antigen receptors (CAR) or gene-modified T cells expressing novel T cell receptors (TCR) may represent a promising alternative approach to modify the immune system to recognize tumor cells with better clinical outcomes. In this review, we briefly discuss the overview of ACT as a promising treatment modality in HCC, along with recent updates of ongoing clinical trials. © 2023 by the authors. | |
| dc.identifier.doi | 10.3390/cancers15061808 | |
| dc.identifier.issn | 2072-6694 | |
| dc.identifier.issue | 6 | |
| dc.identifier.pmcid | PMC10046758 | |
| dc.identifier.pmid | 36980692 | |
| dc.identifier.scopus | 2-s2.0-85151353339 | |
| dc.identifier.startpage | 1808 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/ebyu/12428 | |
| dc.identifier.volume | 15 | |
| dc.language.iso | en | |
| dc.publisher | Multidisciplinary Digital Publishing Institute (MDPI) | |
| dc.relation.ispartof | Cancers | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | adoptive cell therapy | |
| dc.subject | chimeric antigen receptor | |
| dc.subject | clinical trials | |
| dc.subject | hepatocellular carcinoma (HCC) | |
| dc.subject | immunotherapy | |
| dc.subject | T cell receptor | |
| dc.subject | artificial receptor | |
| dc.subject | cancer testis antigen | |
| dc.subject | cyclophosphamide | |
| dc.subject | fludarabine | |
| dc.subject | hepatitis B surface antigen | |
| dc.subject | immune checkpoint inhibitor | |
| dc.subject | mucin 1 | |
| dc.subject | nivolumab | |
| dc.subject | obinutuzumab | |
| dc.subject | oncolytic virus | |
| dc.subject | programmed death 1 receptor | |
| dc.subject | protein tyrosine kinase inhibitor | |
| dc.subject | rituximab | |
| dc.subject | sorafenib | |
| dc.subject | T lymphocyte receptor | |
| dc.subject | transcriptome | |
| dc.subject | acute lymphoblastic leukemia | |
| dc.subject | antigen presenting cell | |
| dc.subject | antineoplastic activity | |
| dc.subject | breast cancer | |
| dc.subject | cancer growth | |
| dc.subject | cancer immunotherapy | |
| dc.subject | cancer patient | |
| dc.subject | CD4+ T lymphocyte | |
| dc.title | Adoptive Cell Therapy in Hepatocellular Carcinoma: A Review of Clinical Trials | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| rdl.citation.scopus | 26 | |
| rdl.department | Department of Medical Oncology, School of Medicine, Erzincan Binali Yildirim University, Erzincan 24100, Turkey. | |
| rdl.oa.status | gold | |
| rdl.source.index | SCOPUS | |
| rdl.source.index | PUBMED |
