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