New Frontiers in the Medical Therapy of Hepatocellular Carcinoma.


Journal

Chemotherapy
ISSN: 1421-9794
Titre abrégé: Chemotherapy
Pays: Switzerland
ID NLM: 0144731

Informations de publication

Date de publication:
2022
Historique:
received: 15 11 2021
accepted: 20 12 2021
pubmed: 10 1 2022
medline: 24 8 2022
entrez: 9 1 2022
Statut: ppublish

Résumé

Hepatocellular carcinoma (HCC) is the most common primary liver tumor, and it rates fourth as a cause of cancer-related death. The presence of underlying liver disease and poor chemosensitivity pose major treatment challenges in the management of HCC. However, in the last few years, the therapeutic scenario has substantially changed, and immunotherapy in the form of immune checkpoint inhibitors (ICPIs) has become an essential therapeutic strategy in this field. After controversial results of monotherapy, ICPIs have been mainly investigated in association with antiangiogenic agents or as dual checkpoint inhibition. The combination of atezolizumab plus bevacizumab has become the new therapeutic standard for unresectable HCC. Currently, a number of ICPI-based combinations are being studied in phase III clinical trials as front-line therapy for advanced HCC, with growing interest in integration of early-stage disease management in the form of adjuvant or neoadjuvant therapies. With most of the trials investigating ICPIs as first-line treatment, the second-line scenario relies mainly on tyrosine kinase inhibitors, which however have not been formally trialed after ICPIs. In this review, we summarize the main therapeutic advances in the systemic management of HCC focusing on the most relevant ongoing trials. We also discuss the main issues arising from a such rapidly evolving field including therapeutic sequencing and patient stratification.

Sections du résumé

BACKGROUND BACKGROUND
Hepatocellular carcinoma (HCC) is the most common primary liver tumor, and it rates fourth as a cause of cancer-related death. The presence of underlying liver disease and poor chemosensitivity pose major treatment challenges in the management of HCC. However, in the last few years, the therapeutic scenario has substantially changed, and immunotherapy in the form of immune checkpoint inhibitors (ICPIs) has become an essential therapeutic strategy in this field.
SUMMARY CONCLUSIONS
After controversial results of monotherapy, ICPIs have been mainly investigated in association with antiangiogenic agents or as dual checkpoint inhibition. The combination of atezolizumab plus bevacizumab has become the new therapeutic standard for unresectable HCC. Currently, a number of ICPI-based combinations are being studied in phase III clinical trials as front-line therapy for advanced HCC, with growing interest in integration of early-stage disease management in the form of adjuvant or neoadjuvant therapies. With most of the trials investigating ICPIs as first-line treatment, the second-line scenario relies mainly on tyrosine kinase inhibitors, which however have not been formally trialed after ICPIs.
KEY MESSAGES CONCLUSIONS
In this review, we summarize the main therapeutic advances in the systemic management of HCC focusing on the most relevant ongoing trials. We also discuss the main issues arising from a such rapidly evolving field including therapeutic sequencing and patient stratification.

Identifiants

pubmed: 34999584
pii: 000521837
doi: 10.1159/000521837
doi:

Substances chimiques

Angiogenesis Inhibitors 0
Bevacizumab 2S9ZZM9Q9V

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

164-172

Informations de copyright

© 2022 The Author(s). Published by S. Karger AG, Basel.

Auteurs

Claudia Angela Maria Fulgenzi (CAM)

Department of Surgery & Cancer, Imperial College London, Hammersmith Hospital, London, United Kingdom.
Department of Medical Oncology, University Campus Bio-Medico, Rome, Italy.

Antonio D'Alessio (A)

Department of Surgery & Cancer, Imperial College London, Hammersmith Hospital, London, United Kingdom.
Department of Biomedical Sciences, Humanitas University, Milan, Italy.

Thomas Talbot (T)

Department of Surgery & Cancer, Imperial College London, Hammersmith Hospital, London, United Kingdom.

Alessandra Gennari (A)

Division of Oncology, Department of Translational Medicine, University of Piemonte Orientale, Novara, Italy.

Mark R Openshaw (MR)

Department of Surgery & Cancer, Imperial College London, Hammersmith Hospital, London, United Kingdom.

Coskun O Demirtas (CO)

Department of Gastroenterology, School of Medicine, Marmara University, Istanbul, Turkey.

Alessio Cortellini (A)

Department of Surgery & Cancer, Imperial College London, Hammersmith Hospital, London, United Kingdom.
Department of Biotechnology and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy.

David J Pinato (DJ)

Department of Surgery & Cancer, Imperial College London, Hammersmith Hospital, London, United Kingdom.
Division of Oncology, Department of Translational Medicine, University of Piemonte Orientale, Novara, Italy.

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Classifications MeSH