Department of Clinical Pharmacy, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran.
Department of Internal Medicine, Ghaem Hospital, Mashhad University of Medical Sciences, Mashhad, Iran.
Cancer Chemother Pharmacol. 2022 Jul;90(1):1-6. doi: 10.1007/s00280-022-04439-x. Epub 2022 May 30.
Ifosfamide is one of the chemotherapy regimens which potentially causes neurotoxicity in patients up to 30%. Aprepitant is administered as an anti-emetic agent in chemotherapy and regarding the inhibitory effect on CYP3A4, aprepitant can increase the risk of ifosfamide adverse effects. This study aims to systematically investigate the relation of ifosfamide-induced neurotoxicity and aprepitant or fosaprepitant in chemotherapy cancer patients. Four databases including PubMed, Scopus, Web of Science, and Embase were systematically reviewed without language restriction and hand searching was performed until December 2021. Total 1639 publications were retrieved and nine studies fulfilled the eligibility criteria. For quality assessment, we used Newcastle-Ottawa quality assessment scales (NOS) for retrospective cohort studies and Cochrane Collaboration tool to assess the risk of bias for a randomized controlled trial. Overall, the results of our systematic review indicated a positive enhanced trend between neurotoxicity and concomitant use of ifosfamide and aprepitant or fosaprepitant, but the association was not statistically significant. As indicated by our findings, several studies identified low albumin as a risk factor for ifosfamide-induced encephalopathy. However, further clinical studies with a larger population of patients are required to evaluate the clinical significance of ifosfamide-related neurotoxicity and aprepitant or fosaprepitant.
异环磷酰胺是一种可能导致多达 30%的患者发生神经毒性的化疗方案之一。阿瑞匹坦作为一种止吐药在化疗中使用,并且由于对 CYP3A4 的抑制作用,阿瑞匹坦可能会增加异环磷酰胺不良反应的风险。本研究旨在系统地调查化疗癌症患者中异环磷酰胺诱导的神经毒性与阿瑞匹坦或福沙匹坦之间的关系。本研究无语言限制地系统检索了 PubMed、Scopus、Web of Science 和 Embase 这四个数据库,并进行了手工检索,检索截止日期为 2021 年 12 月。共检索到 1639 篇出版物,其中 9 项研究符合纳入标准。为了进行质量评估,我们使用纽卡斯尔-渥太华质量评估量表(NOS)评估回顾性队列研究,使用 Cochrane 协作工具评估随机对照试验的偏倚风险。总体而言,我们的系统评价结果表明,神经毒性与异环磷酰胺与阿瑞匹坦或福沙匹坦同时使用之间存在正相关增强趋势,但这种关联没有统计学意义。根据我们的研究结果,一些研究发现低白蛋白是异环磷酰胺诱导脑病的一个危险因素。然而,需要进一步进行具有更大患者人群的临床研究,以评估异环磷酰胺相关神经毒性与阿瑞匹坦或福沙匹坦之间的临床意义。