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瑞戈非尼致肝细胞癌毒性的潜在机制与管理策略。

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

机构信息

College of Pharmaceutical Sciences, Center for Drug Safety Evaluation and Research of Zhejiang University, Hangzhou, China.

Clinical Pharmacy Center, Department of Pharmacy, Zhejiang Provincial People's Hospital, Affiliated People's Hospital, Hangzhou Medical College, Hangzhou, China.

出版信息

Expert Opin Drug Metab Toxicol. 2024 Sep;20(9):907-922. doi: 10.1080/17425255.2024.2398628. Epub 2024 Sep 3.

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.

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.

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.

摘要

简介

肝细胞癌(HCC)占肝癌病例的 85%,是癌症死亡的第三大主要原因。regorafenib 是一种多靶点抑制剂,可显著延长索拉非尼治疗失败的 HCC 患者的无进展生存期。然而,限制regorafenib 临床应用的主要因素之一是其毒性。我们使用 ClinicalTrials.gov 和 PubMed 收集了regorafenib 的临床数据,并对药物的不良反应和机制进行了广泛分析。接下来,我们提出了合适的管理技术来提高 regorafenib 的疗效。

涵盖领域

我们通过对 regorafenib 的临床试验回顾了其诱导毒性的机制和一般管理策略。此外,通过研究 regorafenib 和其他酪氨酸激酶抑制剂的文献,我们总结了 regorafenib 毒性的发生机制和基于机制的干预策略,综述了与 regorafenib 和其他酪氨酸激酶抑制剂相关的文献。

专家意见

限制 regorafenib 临床应用和联合治疗的主要因素之一是其毒性反应。为了优化 regorafenib 治疗方案,深入了解作为多激酶抑制剂的 regorafenib 的特定毒性机制尤为重要。

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