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多形红斑毒素治疗化疗诱导的神经病理性疼痛:一项随机、双盲、安慰剂对照、平行剂量寻找试验。

Tetrodotoxin for Chemotherapy-Induced Neuropathic Pain: A Randomized, Double-Blind, Placebo-Controlled, Parallel-Dose Finding Trial.

机构信息

Hackensack University Medical Center, Hackensack, NJ 07601, USA.

WEX Pharmaceuticals Inc., Vancouver, BC V6E 4A6, Canada.

出版信息

Toxins (Basel). 2021 Mar 25;13(4):235. doi: 10.3390/toxins13040235.

DOI:10.3390/toxins13040235
PMID:33805908
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8064362/
Abstract

Tetrodotoxin (TTX) has emerged as a potentially efficacious agent for chemotherapy-induced neuropathic pain (CINP), a prevalent, debilitating condition often resistant to analgesics. This randomized, double-blind, dose-finding study was undertaken to explore safety and trends in efficacy of four TTX doses and to identify a dose for further study. One hundred and twenty-five patients with taxane- or platinum-related CINP received subcutaneous placebo or TTX (7.5 µg twice daily (BID), 15 µg BID, 30 µg once daily (QD), 30 µg BID) for four consecutive days. Primary outcome measure was average patient-reported Numeric Pain Rating Scale (NPRS) score during Days 21-28 post-treatment. Changes in mean NPRS score were not statistically different between cohorts, due to small trial size and influence of a few robust placebo responders. Cumulative responder analysis showed significant difference from placebo with 30 µg BID cohort using the maximum response at any timepoint ( = 0.072), 5-day ( = 0.059), 10-day ( = 0.027), and 20-day ( = 0.071) rolling averages. In secondary quality of life (QOL) outcomes, 30 µg BID cohort also differed significantly from placebo in a number of SF-36 and CIPN20 subscales. Most adverse events (AE) were mild or moderate with oral paresthesia (29.6%) and oral hypoesthesia (24.8%) as most common.

摘要

河豚毒素 (TTX) 已成为化疗诱导性神经病理性疼痛 (CINP) 的一种有潜力的有效治疗药物,CINP 是一种普遍存在且使人虚弱的疾病,通常对镇痛药有抗性。这项随机、双盲、剂量发现研究旨在探索四种 TTX 剂量的安全性和疗效趋势,并确定进一步研究的剂量。125 名接受紫杉烷或铂类化疗相关 CINP 的患者接受皮下安慰剂或 TTX(7.5 µg 每日两次 (BID)、15 µg BID、30 µg 每日一次 (QD)、30 µg BID)连续四天。主要观察指标为治疗后第 21-28 天患者报告的平均数字疼痛评分量表 (NPRS) 评分。由于试验规模较小且受少数强安慰剂反应者的影响,各队列之间的平均 NPRS 评分变化没有统计学差异。累积应答分析显示,30 µg BID 队列在任何时间点的最大应答(=0.072)、5 天(=0.059)、10 天(=0.027)和 20 天(=0.071)滚动平均值均与安慰剂有显著差异。在次要生活质量 (QOL) 结局中,30 µg BID 队列在多个 SF-36 和 CIPN20 子量表中也与安慰剂有显著差异。大多数不良事件 (AE) 为轻度或中度,最常见的是口腔感觉异常(29.6%)和口腔感觉减退(24.8%)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/291f/8064362/eed83448b719/toxins-13-00235-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/291f/8064362/9433a0628c1f/toxins-13-00235-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/291f/8064362/eed83448b719/toxins-13-00235-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/291f/8064362/9433a0628c1f/toxins-13-00235-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/291f/8064362/eed83448b719/toxins-13-00235-g002.jpg

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