Current understanding of chemotherapy-induced peripheral neuropathy (literature review)

IF 3.2 4区 医学 Q2 CLINICAL NEUROLOGY
O. A. Tikhonova, D. Druzhinin, A. Tynterova, I. Reverchuk
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引用次数: 0

Abstract

This review focuses on chemotherapy-induced polyneuropathy, which is a fairly common side effect and affects not only the quality of life of patients with malignancies, but can also lead to a change in patient management tactics, namely dose modification, delay of drug administration to complete cessation of treatment, which threatens the life of the patient. Chemotherapy-induced polyneuropathy is based on different mechanisms of damaging effects depending on the type of cytotoxic agent. The most neurotoxic drugs are platinum drugs, taxanes, periwinkle alkaloids, bortezomib, and thalidomide. As a result of neurotoxic effects, damage occurs to thin and thick fibers of peripheral nerves. However, it is still a mystery why one patient develops manifestations of neurotoxicity and another does not. Therefore, the modern medical community is faced with the urgent question of further study of the mechanisms of development, risk factors, as well as the search for biomarkers and the development of prevention and treatment of chemotherapy-induced polyneuropathy. The results of studies on the mechanism of onset, clinic, diagnosis, prevention and treatment of chemotherapy-induced polyneuropathies are summarized.
目前对化疗引起的周围神经病变的认识(文献综述)
这篇综述的重点是化疗引起的多神经病变,这是一种相当常见的副作用,不仅影响恶性肿瘤患者的生活质量,而且可能导致患者管理策略的改变,即剂量改变,延迟给药直至完全停止治疗,从而威胁患者的生命。化疗诱导的多神经病变是基于不同的机制的损害作用,这取决于细胞毒素的类型。神经毒性最大的药物是铂类药物、紫杉烷、长春花生物碱、硼替佐米和沙利度胺。由于神经毒性作用,周围神经的细纤维和粗纤维都会受到损伤。然而,为什么一个病人表现出神经毒性而另一个没有,这仍然是一个谜。因此,进一步研究化疗所致多发性神经病的发病机制、危险因素,寻找生物标志物,发展预防和治疗手段,是现代医学界亟待解决的问题。综述了化疗性多神经病变的发病机制、临床、诊断、预防和治疗等方面的研究成果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of neuromuscular diseases
Journal of neuromuscular diseases Medicine-Neurology (clinical)
CiteScore
5.10
自引率
6.10%
发文量
102
期刊介绍: The Journal of Neuromuscular Diseases aims to facilitate progress in understanding the molecular genetics/correlates, pathogenesis, pharmacology, diagnosis and treatment of acquired and genetic neuromuscular diseases (including muscular dystrophy, myasthenia gravis, spinal muscular atrophy, neuropathies, myopathies, myotonias and myositis). The journal publishes research reports, reviews, short communications, letters-to-the-editor, and will consider research that has negative findings. The journal is dedicated to providing an open forum for original research in basic science, translational and clinical research that will improve our fundamental understanding and lead to effective treatments of neuromuscular diseases.
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