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- Publisher Website: 10.1007/s12072-020-10073-7
- Scopus: eid_2-s2.0-85089032113
- PMID: 32661949
- WOS: WOS:000548444900001
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Article: Novel systemic therapy for hepatocellular carcinoma
Title | Novel systemic therapy for hepatocellular carcinoma |
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Authors | |
Keywords | Accelerated approval Adverse events Anti-angiogenesis Combination therapy Cytotoxic T-lymphocyte-associated protein-4 (CTLA-4) |
Issue Date | 2020 |
Publisher | Springer (India) Private Ltd. The Journal's web site is located at http://www.springer.com/medicine/internal/journal/12072 |
Citation | Hepatology International, 2020, v. 14 n. 5, p. 638-651 How to Cite? |
Abstract | Systemic therapy for hepatocellular carcinoma (HCC) used to be limited to patients with advanced diseases and multi-kinase inhibitors targeting tumor angiogenesis the major approach of developing new treatment options. In the past 3 years, new data from trials of both molecular targeted therapy and immune checkpoint inhibitors (ICI) provided many new options of first- and second-line treatment for advanced HCC. Most notably, combination of ICI targeting the program cell death-1 (PD-1) pathway with other novel agents or conventional anti-cancer therapy may further improve treatment efficacy in different clinical settings. In this paper updated data of clinical trials of systemic therapy in the first- and second-line settings for advanced HCC were reviewed and the following issues were discussed: (1) lessons of trial design learned from positive and negative trials; (2) the balance between efficacy and safety in clinical practice; and (3) impact on future multi-disciplinary management of HCC. |
Persistent Identifier | http://hdl.handle.net/10722/305382 |
ISSN | 2023 Impact Factor: 5.9 2023 SCImago Journal Rankings: 1.813 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Dong, Y | - |
dc.contributor.author | Liu, TH | - |
dc.contributor.author | Yau, T | - |
dc.contributor.author | Hsu, C | - |
dc.date.accessioned | 2021-10-20T10:08:37Z | - |
dc.date.available | 2021-10-20T10:08:37Z | - |
dc.date.issued | 2020 | - |
dc.identifier.citation | Hepatology International, 2020, v. 14 n. 5, p. 638-651 | - |
dc.identifier.issn | 1936-0533 | - |
dc.identifier.uri | http://hdl.handle.net/10722/305382 | - |
dc.description.abstract | Systemic therapy for hepatocellular carcinoma (HCC) used to be limited to patients with advanced diseases and multi-kinase inhibitors targeting tumor angiogenesis the major approach of developing new treatment options. In the past 3 years, new data from trials of both molecular targeted therapy and immune checkpoint inhibitors (ICI) provided many new options of first- and second-line treatment for advanced HCC. Most notably, combination of ICI targeting the program cell death-1 (PD-1) pathway with other novel agents or conventional anti-cancer therapy may further improve treatment efficacy in different clinical settings. In this paper updated data of clinical trials of systemic therapy in the first- and second-line settings for advanced HCC were reviewed and the following issues were discussed: (1) lessons of trial design learned from positive and negative trials; (2) the balance between efficacy and safety in clinical practice; and (3) impact on future multi-disciplinary management of HCC. | - |
dc.language | eng | - |
dc.publisher | Springer (India) Private Ltd. The Journal's web site is located at http://www.springer.com/medicine/internal/journal/12072 | - |
dc.relation.ispartof | Hepatology International | - |
dc.rights | Accepted Manuscript (AAM) This is a post-peer-review, pre-copyedit version of an article published in [insert journal title]. The final authenticated version is available online at: https://doi.org/[insert DOI] | - |
dc.subject | Accelerated approval | - |
dc.subject | Adverse events | - |
dc.subject | Anti-angiogenesis | - |
dc.subject | Combination therapy | - |
dc.subject | Cytotoxic T-lymphocyte-associated protein-4 (CTLA-4) | - |
dc.title | Novel systemic therapy for hepatocellular carcinoma | - |
dc.type | Article | - |
dc.identifier.email | Yau, T: tyaucc@hku.hk | - |
dc.identifier.authority | Yau, T=rp01466 | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1007/s12072-020-10073-7 | - |
dc.identifier.pmid | 32661949 | - |
dc.identifier.scopus | eid_2-s2.0-85089032113 | - |
dc.identifier.hkuros | 326653 | - |
dc.identifier.volume | 14 | - |
dc.identifier.issue | 5 | - |
dc.identifier.spage | 638 | - |
dc.identifier.epage | 651 | - |
dc.identifier.isi | WOS:000548444900001 | - |
dc.publisher.place | India | - |