Cancer Research Center, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences, Tehran, Iran.
Radiation Oncology Department, Cancer Institute, Imam-Khomeini Hospital Complex, Tehran University of Medical Sciences, Tehran, Iran.
Support Care Cancer. 2024 Jul 8;32(8):493. doi: 10.1007/s00520-024-08669-y.
Chemotherapy-induced peripheral neuropathy (CIPN) is one of the major side effects and main reasons for affecting quality of life and dose reduction or even discontinuation of treatment in breast cancer patients. One of the most widely prescribed chemotherapies is the "taxanes." Considering that duloxetine has been used in treating neuropathies in recent years, this study aimed to investigate its effectiveness in preventing taxane-related neuropathy.
This is a randomized controlled trial on 47 patients: 24 received a placebo and 23 received duloxetine at 30 mg daily in the first week following the injection of paclitaxel and 60 mg during the second week in each chemotherapy cycle. Patients objective (nerve conduction velocity (NCV) values) and subjective symptoms (visual analog scale including; neuropathy, paresthesia, pain, cold sensitivity, and numbness), the grades of the patients' neuropathy (calculated according to Common Terminology Criteria for Adverse Events (CTCAE) v.5), and the presence of complications, before and after each chemotherapy cycle, were recorded.
The placebo group experienced significantly higher occurrences of new neuropathy (8/23 in duloxetine vs 16/24 in placebo, P = 0.029) in NCV by tibial nerve latency (- 0.28% vs 19.87%, P = 0.006), tibial amplitude (4.40% vs - 10.88%, P = 0.049), and median nerve latency (8.72% vs 31.16%, P = 0.039); administration of duloxetine significantly reduced the scores of neuropathies (P < 0.001), pain (P = 0.027), during chemotherapy, and 6 weeks later; however, no significant effect was observed on paresthesia, numbness, cold sensitivity, and other NCV measurements.
Paclitaxel can cause neuropathy, lasting for a long time. Our study showed duloxetine is potentially an effective medication that can prevent subjective and objective neuropathy.
化疗引起的周围神经病变(CIPN)是乳腺癌患者生活质量下降、减少剂量甚至停止治疗的主要副作用和主要原因之一。最广泛使用的化疗药物之一是“紫杉烷”。鉴于度洛西汀近年来已用于治疗神经病变,本研究旨在探讨其预防紫杉烷相关神经病变的效果。
这是一项针对 47 名患者的随机对照试验:24 名患者接受安慰剂,23 名患者在紫杉醇注射后第一周内每天接受 30mg 度洛西汀,在每个化疗周期的第二周内接受 60mg 度洛西汀。记录患者的客观(神经传导速度(NCV)值)和主观症状(包括神经病变、感觉异常、疼痛、冷敏和麻木的视觉模拟量表)、患者神经病变的程度(根据不良事件通用术语标准(CTCAE)v.5 计算)以及并发症的发生情况,在每个化疗周期前后。
安慰剂组在 NCV 中的新神经病变发生率明显更高(度洛西汀组 8/23,安慰剂组 16/24,P=0.029),胫骨神经潜伏期(-0.28%比 19.87%,P=0.006),胫骨振幅(4.40%比-10.88%,P=0.049)和正中神经潜伏期(8.72%比 31.16%,P=0.039);度洛西汀的给药显著降低了神经病变(P<0.001)、疼痛(P=0.027)的评分在化疗期间和 6 周后;然而,在感觉异常、麻木、冷敏和其他 NCV 测量方面没有观察到显著效果。
紫杉醇可引起神经病变,持续时间长。我们的研究表明,度洛西汀可能是一种有效的预防药物,可预防主观和客观的神经病变。