Literature DB >> 33052638

A concise review of the changing landscape of hepatocellular carcinoma.

Amber Draper1.   

Abstract

Hepatocellular carcinoma (HCC) is the fastest rising cause of cancer-related deaths in the United States, increasing by 2% to 3% annually, with a dismal 5-year survival rate of 18%. The Barcelona Clinic Liver Cancer criteria used to guide treatment considers performance status and assessment of liver function by Child-Pugh score in addition to tumor size and location. Curative therapies for HCC include surgical resection, liver transplantation, and tumor ablation. Patients with unresectable or inoperable lesions should be considered for arterially directed embolic therapy, systemic therapy, or radiation. Options for first-line systemic therapy of advanced HCC include sorafenib, lenvatinib, and atezolizumab plus bevacizumab. Nivolumab may be an option in patients with advanced HCC who are ineligible for tyrosine kinase inhibitors or other anti-angiogenic agents. Options for subsequent therapy following disease progression include regorafenib, cabozantinib, ramucirumab, lenvatinib, nivolumab, nivolumab plus ipilimumab, sorafenib, or pembrolizumab. Patients with advanced HCC are at a high risk of adverse effects because of baseline hepatic dysfunction, comorbidities associated with chronic liver disease, and potential drug-drug interactions. Improved tolerance of therapies for advanced HCC may lead to reduction in treatment discontinuation and contribute to better patient outcomes. Managed care pharmacists should understand the recent efficacy and safety data, guideline recommendations, and treatment algorithms for management of HCC.

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Year:  2020        PMID: 33052638     DOI: 10.37765/ajmc.2020.88512

Source DB:  PubMed          Journal:  Am J Manag Care        ISSN: 1088-0224            Impact factor:   2.229


  4 in total

1.  Combined inhibition of FGFR4 and VEGFR signaling enhances efficacy in FGF19 driven hepatocellular carcinoma.

Authors:  Xuesong Zhao; Jaya Julie Joshi; Daniel Aird; Craig Karr; Kun Yu; Chialing Huang; Federico Colombo; Milena Virrankoski; Sudeep Prajapati; Anand Selvaraj
Journal:  Am J Cancer Res       Date:  2022-06-15       Impact factor: 5.942

2.  Influence of schisantherin A on the pharmacokinetics of lenvatinib in rats and its potential mechanism.

Authors:  Yanjun Cui; Yinling Ma; Ying Li; Haojing Song; Zhanjun Dong
Journal:  J Gastrointest Oncol       Date:  2022-04

3.  Upregulation of GTPBP4 Promotes the Proliferation of Liver Cancer Cells.

Authors:  Jia Chen; Jie Zhang; Zhiwei Zhang
Journal:  J Oncol       Date:  2021-10-19       Impact factor: 4.375

4.  Lenvatinib in patients with unresectable hepatocellular carcinoma who progressed to Child-Pugh B liver function.

Authors:  Jasmine Huynh; May Thet Cho; Edward Jae-Hoon Kim; Min Ren; Zahra Ramji; Arndt Vogel
Journal:  Ther Adv Med Oncol       Date:  2022-08-24       Impact factor: 5.485

  4 in total

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