Cavaletti Guido, Marmiroli Paola
Università di Milano Bicocca, Dipartimento di Neuroscienze e Tecnologie Biomediche, v. Cadore 48, 20052 Monza (MI), Italia.
Expert Opin Drug Saf. 2004 Nov;3(6):535-46. doi: 10.1517/14740338.3.6.535.
Chemotherapy-induced peripheral neurotoxicity (CIPN) is a major clinical problem because it represents the dose-limiting side effects of a significant number of antineoplastic drugs. The incidence of CIPN varies depending on the drugs and schedules used, and this can be quite high, particularly when neurophysiological methods are used to make a diagnosis. However, even when CIPN is not a dose-limiting side effect, its onset may severely affect the quality of life of cancer patients and cause chronic discomfort. In this review the features of CIPN due to the administration of the most widely used drugs, such as platinum drugs, taxanes and vinca alkaloids, and of two old drugs with new clinical applications, suramin and thalidomide, will be discussed. Moreover, the earliest data regarding the neurotoxicity of some new classes of very promising antineoplastic agents, such as epothilones and proteasome inhibitors, will be discussed. Finally, the data available on neuroprotectants, evaluated in the attempt to prevent CIPN, will be summarised.
化疗引起的周围神经毒性(CIPN)是一个主要的临床问题,因为它是许多抗肿瘤药物的剂量限制性副作用。CIPN的发生率因所用药物和方案而异,可能相当高,尤其是在使用神经生理学方法进行诊断时。然而,即使CIPN不是剂量限制性副作用,其发作也可能严重影响癌症患者的生活质量并导致慢性不适。在本综述中,将讨论由于使用最广泛的药物(如铂类药物、紫杉烷类和长春花生物碱)以及两种具有新临床应用的老药(苏拉明和沙利度胺)引起的CIPN的特征。此外,还将讨论关于一些非常有前景的新型抗肿瘤药物(如埃坡霉素和蛋白酶体抑制剂)神经毒性的最新数据。最后,将总结为预防CIPN而评估的神经保护剂的现有数据。