肝细胞癌中瑞戈非尼诱发毒性的基本机制和管理策略。

Mengting Cheng, Xinyu Tao, Fei Wang, Nonger Shen, Zhifei Xu, Yuhuai Hu, Ping Huang, Peihua Luo, Qiaojun He, Yiwen Zhang, Fangjie Yan
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引用次数: 0

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原因。瑞戈非尼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,限制瑞戈非尼临床应用的主要因素之一是毒性。我们利用 Clinical Trials.gov 和 PubMed 收集了瑞戈非尼的临床数据,并对该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巧,以提高瑞戈非尼的疗效:我们通过瑞戈非尼的临床试验,回顾了瑞戈非尼诱发毒性的发生机制和一般管理策略。此外,通过研究瑞戈非尼和其他酪氨酸激酶抑制剂的相关文献,我们总结了瑞戈非尼毒性发生的机理以及基于机理的干预策略:专家观点:瑞戈非尼的毒性反应是制约其临床应用和联合治疗的主要因素之一。为优化瑞戈非尼治疗方案,进一步了解瑞戈非尼作为多激酶抑制剂的特殊毒性机制尤为重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Underlying mechanisms and management strategies for regorafenib-induced toxicity in hepatocellular carcinoma.

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.

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