褪黑素对紫杉醇相关急性和慢性疼痛的影响:一项随机、双盲、安慰剂对照的临床试验

Q4 Pharmacology, Toxicology and Pharmaceutics
N. Talaee, S. Ebrahimpour, Mohsen Sfandbod, H. Majedi, Aarefeh Jafarzadeh Kohneloo, K. Gholami, Z. Jahangard-Rafsanjani
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引用次数: 1

摘要

背景:紫杉烷引起的疼痛是一种致残性疾病。本试验旨在评估褪黑素对乳腺癌患者预防紫杉醇相关急性和慢性疼痛或降低其严重程度的作用。方法:这项随机、双盲、安慰剂对照的临床试验是在使用阿霉素+环磷酰胺后,每周接受紫杉醇(80 mg/m2)治疗或不接受曲妥珠单抗治疗的乳腺癌妇女。干预组随机给予口服褪黑素(10mg /天)或安慰剂,从化疗的第一个晚上开始,持续到计划的12周化疗。两组患者每天使用简短疼痛量表(BPI)评估急性疼痛的关节痛-肌痛水平。采用Douleur neuropathque 4问卷(DN4)和美国国家癌症研究所不良事件通用术语标准(NCI-CTCAE) 5.0版来测量化疗引起的周围神经病变为慢性疼痛。结果:每组随机入组17例。根据DN4评分≥4,与基线相比,褪黑素组在第12周的神经病变发生率显著低于安慰剂组(5 vs 11, p值= 0.039)。此外,随着时间的推移,褪黑激素组的平均神经病变严重程度显著降低(β= -0.051, p值= 0.01)。然而,在12个治疗周期内,两组患者的平均最差和最低疼痛评分无显著差异(p值分别为0.633,0.341)。结论:乳腺癌患者联合使用褪黑素可降低严重紫杉醇相关神经病变的发生率,但对急性疼痛无效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of melatonin on paclitaxel-associated acute and chronic pain: a randomized, double-blind, placebo-controlled clinical trial
Background: Taxane-induced pain is a disabling condition. This trial was conducted to assess the effects of melatonin on preventing paclitaxel-associated acute and chronic pain or decreasing its severity in patients with breast cancer. Methods: This randomized, double-blind, placebo-controlled clinical trial was conducted on breast cancer women who received weekly paclitaxel (80 mg/m2) with or without trastuzumab after using doxorubicin + cyclophosphamide. The intervention group randomly received oral melatonin (10 mg/day) or placebo, which started from the first night of chemotherapy and continued through the planned 12 weeks of chemotherapy. The level of arthralgia-myalgia as acute pain was assessed every day in both groups using the Brief Pain Inventory (BPI). The Douleur Neuropathique 4 questionnaire (DN4) and National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE) version 5.0 were used to measure chemotherapy-induced peripheral neuropathy as chronic pain. Results: Seventeen patients were enrolled in each group randomly. The incidence of neuropathy according to a DN4 score ≥ 4 was significantly lower in the melatonin group versus the placebo group at week 12 compared to baseline (5 vs 11, P-value= 0.039). In addition, the mean neuropathy severity was significantly lower in the melatonin group over time (β= -0.051, P-value= 0.01). However, there were no significant differences in the mean worst and least pain scores over the twelve cycles of treatment between arms (P-value= 0.633, 0.341 respectively). Conclusion: Co-administration of melatonin in women with breast cancer decreased the incidence of severe paclitaxel-associated neuropathy but melatonin was not effective against acute pain.
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CiteScore
0.10
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17
审稿时长
10 weeks
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