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无线经皮神经电刺激(TENS)治疗慢性化疗诱导的周围神经病(CIPN):一项概念验证随机临床试验。

Wireless Transcutaneous Electrical Nerve Stimulation (TENS) for Chronic Chemotherapy-Induced Peripheral Neuropathy (CIPN): A Proof-of-Concept Randomized Clinical Trial.

机构信息

Department of Anesthesiology and Perioperative Medicine, University of Rochester Medical Center, Rochester, New York.

Department of Surgery, Supportive Care in Cancer, University of Rochester Medical Center, Rochester, New York.

出版信息

J Pain. 2024 May;25(5):104431. doi: 10.1016/j.jpain.2023.11.014. Epub 2023 Nov 21.

Abstract

Chemotherapy-induced peripheral neuropathy (CIPN) affects approximately 30 to 60% of people who receive neurotoxic chemotherapy. CIPN is associated with impaired quality of life and function and has few effective treatments. This 6-site, subject and assessor-blinded randomized clinical trial (RCT) was designed to assess 1) preliminary efficacy (ie, alpha pre-specified at .2) of a wearable, app-controlled, transcutaneous electrical nerve stimulation (TENS) device for chronic CIPN and 2) feasibility of conducting a confirmatory trial within the National Cancer Institute Community Oncology Research Program (NCORP) (NCT04367480). The primary outcome was the EORTC-CIPN20. The main secondary outcomes were individual symptoms assessed daily (via 0-10 numeric rating scales). The primary analysis was an analysis of covariance (outcome: EORTC-CIPN20, fixed effect: arm, covariates: baseline EORTC-CIPN20 and site). Secondary analyses used a similar analysis of covariance models (excluding site) for each symptom on subgroups of subjects with ≥4 out of 10 for that symptom at baseline. 142 eligible subjects were randomized and received a device; 130 (91%) completed the study. The difference between groups in the EORCT-CIPN20 at the endpoint (placebo-active) was 1.05 (95% Confidence Interval: -.56, 2.67; P = .199). The difference between groups for the individual symptoms was as follows: hot/burning pain: 1.37 (-.33, 3.08; P = .112), sharp/shooting pain: 1.21 (-.37, 2.79; P = .128), cramping: 1.35 (-.32, 3.02; P = .110), tingling: .23 (-.61, 1.08; P = .587), numbness: .27 (-.51, 1.05; P = .492). An RCT of an app-controlled TENS device for chronic CIPN with excellent retention is feasible in the NCORP. Preliminary efficacy evidence suggests that TENS is promising for pain and cramping from CIPN. A confirmatory RCT of TENS for painful CIPN is highly warranted. PERSPECTIVE: Daily, home-based TENS therapy demonstrates promising efficacy for painful CIPN symptoms in this proof-of-concept randomized clinical trial. Future confirmatory trial is warranted.

摘要

化疗引起的周围神经病(CIPN)影响大约 30%至 60%接受神经毒性化疗的人。CIPN 与生活质量和功能受损有关,且治疗方法有限。本项 6 个地点、受试者和评估者盲法随机临床试验(RCT)旨在评估 1)一种可穿戴、应用程序控制的经皮神经电刺激(TENS)设备治疗慢性 CIPN 的初步疗效(即,α 预先指定为.2)和 2)在国家癌症研究所社区肿瘤学研究计划(NCORP)内进行确证性试验的可行性(NCT04367480)。主要结局是 EORTC-CIPN20。主要次要结局是每天评估的个体症状(通过 0-10 数字评分量表)。主要分析是协方差分析(结局:EORTC-CIPN20,固定效应:手臂,协变量:基线 EORTC-CIPN20 和地点)。次要分析使用类似的协方差模型(排除地点),用于每个症状的亚组,该亚组在基线时该症状的评分≥10 分中的 4 分。符合条件的 142 名受试者被随机分配并接受设备;130 名(91%)完成了研究。终点(安慰剂-活性)时组间 EORCT-CIPN20 的差异为 1.05(95%置信区间:-.56,2.67;P =.199)。个体症状组间差异如下:灼热/灼痛:1.37(-.33,3.08;P =.112),刺痛/刺痛:1.21(-.37,2.79;P =.128),痉挛:1.35(-.32,3.02;P =.110),刺痛:.23(-.61,1.08;P =.587),麻木:.27(-.51,1.05;P =.492)。NCORP 中进行的一项用于慢性 CIPN 的应用程序控制 TENS 设备的 RCT 具有极好的保留率是可行的。初步疗效证据表明,TENS 对 CIPN 引起的疼痛和痉挛有希望。针对 CIPN 疼痛的 TENS 确证性 RCT 非常有必要。观点:这项概念验证随机临床试验中,每日家庭 TENS 治疗对 CIPN 疼痛症状显示出有希望的疗效。未来的确证性试验是必要的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c33/11058028/7a85ab8ea986/nihms-1947401-f0001.jpg

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