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The evolution of immune checkpoint inhibitor combinations in advanced hepatocellular carcinoma - A systematic review.
Meyers, Brandon M; Knox, Jennifer J; Liu, David M; McLeod, Deanna; Ramjeesingh, Ravi; Tam, Vincent C; Lim, Howard J.
Affiliation
  • Meyers BM; Juravinski Cancer Centre, McMaster University, 699 Concession St, Hamilton, ON L8V 5C2, Canada. Electronic address: meyersbr@HHSC.CA.
  • Knox JJ; Princess Margaret Cancer Centre, University of Toronto, 610 University Ave, Toronto, ON M5G 2C4, Canada. Electronic address: Jennifer.knox@uhn.ca.
  • Liu DM; School of Biomedical Engineering, University of British Columbia, 2329 West Mall, Vancouver, BC V6T 1Z4, Canada. Electronic address: Dave.Liu@vch.ca.
  • McLeod D; Kaleidoscope Strategic, Inc. 1 King Street W, Suite 4800 - 117, Toronto, ON M5H 1A1, Canada. Electronic address: deanna@kstrategic.com.
  • Ramjeesingh R; Department of Medicine, Dalhousie University, 6299 South St, Halifax, NS B3H 4R2, Canada. Electronic address: Ravi.Ramjeesingh@nshealth.ca.
  • Tam VC; Tom Baker Cancer Centre, University of Calgary, 1331 29 St NW, Calgary, AB T2N 4N2, Canada. Electronic address: Vincent.Tam@albertahealthservices.ca.
  • Lim HJ; BC Cancer Agency, 600 West 10th Avenue, Vancouver, BC V5Z 4E6, Canada. Electronic address: hlim@bccancer.bc.ca.
Cancer Treat Rev ; 118: 102584, 2023 Jul.
Article in En | MEDLINE | ID: mdl-37336142
ABSTRACT
BACKGROUND AND

OBJECTIVE:

Since approval of sorafenib in 2008, systemic therapy has been established as the main treatment option for advanced hepatocellular carcinoma (HCC). Recently, immune checkpoints inhibitors (ICIs) have been extensively tested in this setting. Multiple ICI combination regimens have recently received regulatory approval and new data continues to emerge. The purpose of this review is to provide a comprehensive summary of the most up-to-date evidence on ICI combinations in advanced HCC.

METHODS:

A search of published and presented literature was conducted to identify phase III trials of ICI combinations in advanced HCC patients. Supplemental bibliographic search of review articles and meta-analyses was also conducted. Efficacy and safety data was summarized in text, tables, and plots. FINDINGS AND

DISCUSSION:

The literature search identified a total of six phase III trials assessing ICI combinations in advanced HCC. Two trials compared ICI plus anti-VEGF monoclonal antibody combinations to sorafenib, three trials compared ICI plus tyrosine kinase inhibitor (TKI) combinations to TKIs alone, and one trial compared a dual ICI regimen to sorafenib. Statistically significant survival benefits were seen with atezolizumab-bevacizumab and sintilimab-bevacizumab biosimilar as well as durvalumab-tremelimumab and camrelizumab-rivoceranib combinations. ICI combination regimens have also shown improvements in response rates and progression-free survival relative to the previous standard of care, sorafenib, and generally presented predictable and manageable safety profiles.

CONCLUSION:

ICI combinations represent the new standard of care for advanced HCC. Ongoing randomized trials and real-world evidence will further clarify the role of these combinations in this rapidly evolving field.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Carcinoma, Hepatocellular / Liver Neoplasms Type of study: Clinical_trials / Prognostic_studies / Systematic_reviews Limits: Humans Language: En Journal: Cancer Treat Rev Year: 2023 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Carcinoma, Hepatocellular / Liver Neoplasms Type of study: Clinical_trials / Prognostic_studies / Systematic_reviews Limits: Humans Language: En Journal: Cancer Treat Rev Year: 2023 Document type: Article