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奥沙利铂诱导的结直肠癌神经病变:诸多疑问,尚无答案。

Oxaliplatin-induced neuropathy in colorectal cancer: many questions with few answers.

机构信息

Department of Oncology, Lillebaelt Hospital, Vejle, Denmark.

Neurobiology Research, University of Southern Denmark.

出版信息

Clin Colorectal Cancer. 2014 Jun;13(2):73-80. doi: 10.1016/j.clcc.2013.11.004. Epub 2013 Nov 13.

Abstract

Oxaliplatin is a chemotherapeutic agent effective against advanced colorectal cancer. Unlike with other platinum-based agents, the main side effect of oxaliplatin is polyneuropathy. Oxaliplatin-induced polyneuropathy (OIPN) has a unique profile, which can be divided into acute and chronic neurotoxicity. Early identification of the neurotoxicity and alterations in dose or schedule for the medication could prevent the development of chronic symptoms, which, once established, may take many months or years to resolve or even persist throughout life with a substantial effect on quality of life. There is no doubt that the use of pharmacogenomic methods to identify genetic bases of interindividual differences in drug response has led to what is called tailoring treatment. Yet there are some challenges regarding the application of these differences. Many efforts have been made to prevent or treat OIPN. Better understanding of the mechanisms underlying the acute and chronic forms of OIPN will be a key component of future advances in the prevention and treatment of OIPN. The aim of this review is to highlight the clinical presentation, assessment, and management of OIPN, as well as the underlying pathophysiologic and pharmacogenomic background.

摘要

奥沙利铂是一种有效的化疗药物,可用于治疗晚期结直肠癌。与其他铂类药物不同,奥沙利铂的主要副作用是周围神经病变。奥沙利铂引起的周围神经病变(OIPN)具有独特的特征,可分为急性和慢性神经毒性。早期识别神经毒性以及调整药物剂量或方案可以预防慢性症状的发生,一旦出现慢性症状,可能需要数月甚至数年才能缓解,甚至会持续终生,对生活质量产生重大影响。毫无疑问,使用药物基因组学方法来确定药物反应个体差异的遗传基础已经导致了所谓的个体化治疗。然而,这些差异的应用存在一些挑战。人们已经做出了许多努力来预防或治疗 OIPN。更好地了解 OIPN 的急性和慢性形式的潜在机制将是预防和治疗 OIPN 未来进展的关键组成部分。本文旨在强调 OIPN 的临床表现、评估和管理,以及潜在的病理生理和药物基因组学背景。

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