口服大麻治疗紫杉烷诱导的神经病变:一项随机安慰剂对照研究。

IF 3.1 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Margaret Haney, Tse-Hwei Choo, Amy Tiersten, Frances R Levin, Alex Grassetti, Natasha DeSilva, Caroline A Arout, Diana Martinez
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引用次数: 0

摘要

简介:紫杉烷诱导的周围神经病变(TIPN)是大多数乳腺癌患者的症状,目前尚无有效的治疗方法。在临床前研究中,联合使用大麻的两种成分Δ9-tetrahydrocannabinol (THC)和大麻二酚(CBD)可以协同降低TIPN。材料和方法:这项为期8周的双盲随机先导研究于2019年至2021年进行,目的是测试口服大麻(100 mg CBD: 5 mg THC, TID)相对于安慰剂对TIPN引起的疼痛的可行性和耐受性。患有疼痛性TIPN的参与者每天在线完成关于疼痛、睡眠和药物使用的问卷调查,并每周完成关于神经病变的问卷调查。结果:所有参与者(12名女性;51±6年)随机分为安慰剂组(n = 6)或活性大麻胶囊组(n = 6)完成试验。两个用药组的参与者都要求减少剂量(平均±SEM胶囊/天:安慰剂:2.4±0.4;活性:2.0±0.4)。在对疗效的初步评估中,疼痛、疼痛干扰、睡眠和功能健康的测量随着时间的推移显着改善(p < 0.03),但与接受安慰剂的参与者相比,接受大麻治疗的参与者每周的神经病变评分明显较高(p < 0.035),而在治疗的最后3周的功能健康评分较低(p < 0.02)。同样,与安慰剂相比,大麻显著加重了睡眠和疼痛干扰评分(p < 0.05)。讨论:本研究表明:(1)在该剂量范围内对大麻胶囊进行双盲、安慰剂对照试验是可行的,并且对患有TIPN的女性具有良好的耐受性;(2)疼痛、神经病变和幸福感评分在8周内显著改善,但与安慰剂相比,大麻显著恶化了几个终点。这些发现强调了在评估大麻的治疗效用时进行安慰剂对照的必要性。虽然这里没有疗效的信号,但考虑到TIPN对大多数乳腺癌患者的影响,有希望的临床前数据,以及癌症患者中大麻的广泛使用,有必要对一系列大麻剂量进行全面的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Oral Cannabis for Taxane-Induced Neuropathy: A Pilot Randomized Placebo-Controlled Study.

Introduction: Taxane-induced peripheral neuropathy (TIPN) is experienced by most patients with breast cancer, and there is no efficacious treatment. In pre-clinical studies, co-administration of two constituents of cannabis, Δ9-tetrahydrocannabinol (THC) and cannabidiol (CBD), synergistically reduces TIPN. Materials and Methods: The goal of this 8-week, double-blind, randomized pilot study, conducted from 2019 to 2021, was to test the feasibility and tolerability of oral cannabis (100 mg CBD: 5 mg THC, TID) relative to placebo on pain resulting from TIPN. Participants with painful TIPN completed daily questionnaires online about their pain, sleep, and medication use, and weekly questionnaires on neuropathy. Results: All participants (12 women; 51 ± 6 years) randomized to placebo (n = 6) or active (n = 6) cannabis capsules completed the trial. Participants in both medication groups requested dose reductions (mean ± SEM capsules/day: placebo: 2.4 ± 0.4; active: 2.0 ± 0.4). In a preliminary evaluation of efficacy, measures of pain, pain interference, sleep, and functional well-being significantly improved over time (p < 0.03), but participants receiving cannabis had significantly higher ratings of neuropathy at each week (p < 0.035) and lower ratings of functional well-being in the last 3 weeks of treatment compared with participants receiving placebo (p < 0.02). Similarly, cannabis significantly worsened ratings of sleep and pain interference relative to placebo (p < 0.05). Discussion: This study demonstrates that: (1) double-blind, placebo-controlled testing of cannabis capsules in this dose range is feasible and well tolerated in women with TIPN and (2) ratings of pain, neuropathy, and well-being significantly improved over 8 weeks, but cannabis significantly worsened several endpoints relative to placebo. These findings highlight the necessity of placebo control when assessing the therapeutic utility of cannabis. Although there was no signal of efficacy herein, a fully powered study testing a range of cannabis doses for TIPN is warranted, given its impact on most patients with breast cancer, promising pre-clinical data, and the widespread use of cannabis among patients with cancer.

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来源期刊
Cannabis and Cannabinoid Research
Cannabis and Cannabinoid Research PHARMACOLOGY & PHARMACY-
CiteScore
6.80
自引率
7.90%
发文量
164
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