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Underlying mechanisms and management strategies for regorafenib-induced toxicity in hepatocellular carcinoma.

Authors :
Cheng M
Tao X
Wang F
Shen N
Xu Z
Hu Y
Huang P
Luo P
He Q
Zhang Y
Yan F
Source :
Expert opinion on drug metabolism & toxicology [Expert Opin Drug Metab Toxicol] 2024 Sep 03, pp. 1-16. Date of Electronic Publication: 2024 Sep 03.
Publication Year :
2024
Publisher :
Ahead of Print

Abstract

Introduction: Hepatocellular carcinoma (HCC) accounts for 85% of liver cancer cases and is the third leading cause of cancer death. Regorafenib is a multi-target inhibitor that dramatically prolongs progression-free survival in HCC patients who have failed sorafenib therapy. However, one of the primary factors limiting regorafenib's clinical utilization is toxicity. Using Clinical Trials.gov and PubMed, we gathered clinical data on regorafenib and conducted a extensive analysis of the medication's adverse reactions and mechanisms. Next, we suggested suitable management techniques to improve regorafenib's effectiveness.<br />Areas Covered: We have reviewed the mechanisms by which regorafenib-induced toxicity occurs and general management strategies through clinical trials of regorafenib. Furthermore, by examining the literature on regorafenib and other tyrosine kinase inhibition, we summarized the mechanics of the onset of regorafenib toxicity and mechanism-based intervention strategies by reviewing the literature related to regorafenib and other tyrosine kinase inhibition.<br />Expert Opinion: One of the primary factors restricting regorafenib's clinical utilization and combination therapy is its toxicity reactions. To optimize regorafenib treatment regimens, it is especially important to further understand the specific toxicity mechanisms of regorafenib as a multi-kinase inhibitor.

Details

Language :
English
ISSN :
1744-7607
Database :
MEDLINE
Journal :
Expert opinion on drug metabolism & toxicology
Publication Type :
Academic Journal
Accession number :
39225462
Full Text :
https://doi.org/10.1080/17425255.2024.2398628