Angiogenesis in Hepatocellular Carcinoma; Pathophysiology, Targeted Therapy, and Role of Imaging.

Sorafenib angiogenesis anti-angiogenic therapy hepatocellular carcinoma

Journal

Journal of hepatocellular carcinoma
ISSN: 2253-5969
Titre abrégé: J Hepatocell Carcinoma
Pays: New Zealand
ID NLM: 101674775

Informations de publication

Date de publication:
2020
Historique:
received: 24 07 2019
accepted: 24 12 2019
entrez: 20 5 2020
pubmed: 20 5 2020
medline: 20 5 2020
Statut: epublish

Résumé

Hepatocellular carcinoma (HCC) is one of the most common tumors worldwide, usually occurring on a background of liver cirrhosis. HCC is a highly vascular tumor in which angiogenesis plays a major role in tumor growth and spread. Tumor-induced angiogenesis is usually related to a complex interplay between multiple factors and pathways, with vascular endothelial growth factor being a major player in angiogenesis. In the past decade, understanding of tumor-induced angiogenesis has led to the emergence of novel anti-angiogenic therapies, which act by reducing neo-angiogenesis, and improving patient survival. Currently, Sorafenib and Lenvatinib are being used as the first-line treatment for advanced unresectable HCC. However, a disadvantage of these agents is the presence of numerous side effects. A major challenge in the management of HCC patients being treated with anti-angiogenic therapy is effective monitoring of treatment response, which decides whether to continue treatment or to seek second-line treatment. Several criteria can be used to assess response to treatment, such as quantitative perfusion on cross-sectional imaging and novel/emerging MRI techniques, including a host of known and emerging biomarkers and radiogenomics. This review addresses the pathophysiology of angiogenesis in HCC, accurate imaging assessment of angiogenesis, monitoring effects of anti-angiogenic therapy to guide future treatment and assessing prognosis.

Identifiants

pubmed: 32426302
doi: 10.2147/JHC.S224471
pii: 224471
pmc: PMC7188073
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

77-89

Informations de copyright

© 2020 Moawad et al.

Déclaration de conflit d'intérêts

The authors report no conflicts of interest in this work.

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Auteurs

Ahmed W Moawad (AW)

Department of Diagnostic Radiology, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.

Janio Szklaruk (J)

Department of Diagnostic Radiology, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.

Chandana Lall (C)

Department of Radiology, University of Florida College of Medicine, Jacksonville, FL, USA.

Katherine J Blair (KJ)

Department of Diagnostic Radiology, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.

Ahmed O Kaseb (AO)

Department of Gastrointestinal Oncology, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.

Amita Kamath (A)

Department of Radiology, Icahn School of Medicine at Mount Sinai West, New York, NY, USA.

Scott A Rohren (SA)

School of Medicine, Baylor College of Medicine, Houston, TX, USA.

Khaled M Elsayes (KM)

Department of Diagnostic Radiology, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.

Classifications MeSH