随机电针对芳香化酶抑制剂相关关节痛的临床试验。
A randomised trial of electro-acupuncture for arthralgia related to aromatase inhibitor use.
机构信息
Department of Family Medicine and Community Health, Perelman School of Medicine at the University of Pennsylvania, PA, United States; Center for Clinical Epidemiology and Biostatistics and Department of Biostatistics and Epidemiology, Perelman School of Medicine at the University of Pennsylvania, PA, United States; Abramson Cancer Center, Perelman School of Medicine at the University of Pennsylvania, PA, United States.
Center for Clinical Epidemiology and Biostatistics and Department of Biostatistics and Epidemiology, Perelman School of Medicine at the University of Pennsylvania, PA, United States.
出版信息
Eur J Cancer. 2014 Jan;50(2):267-76. doi: 10.1016/j.ejca.2013.09.022. Epub 2013 Oct 24.
BACKGROUND
Arthralgia is a common and debilitating side-effect experienced by breast cancer patients receiving aromatase inhibitors (AIs) and often results in premature drug discontinuation.
METHODS
We conducted a randomised controlled trial of electro-acupuncture (EA) as compared to waitlist control (WLC) and sham acupuncture (SA) in postmenopausal women with breast cancer who self-reported arthralgia attributable to AIs. Acupuncturists performed 10 EA/SA treatments over 8 weeks using a manualised protocol with 2 Hz electro-stimulation delivered by a TENS unit. Acupuncturists administered SA using Streitberger (non-penetrating) needles at non-traditional acupuncture points without electro-stimulation. The primary end-point was pain severity by Brief Pain Inventory (BPI) between EA and WLC at Week 8; durability of response at Week 12 and comparison of EA to SA were secondary aims.
FINDINGS
Of the 67 randomly assigned patients, mean reduction in pain severity was greater in the EA group than in the WLC group at Week 8 (-2.2 versus -0.2, p=0.0004) and at Week 12 (-2.4 versus -0.2, p<0.0001). Pain-related interference measured by BPI also improved in the EA group compared to the WLC group at both Week 8 (-2.0 versus 0.2, p=0.0006) and Week 12 (-2.1 versus -0.1, p=0.0034). SA produced a magnitude of change in pain severity and pain-related interference at Week 8 (-2.3, -1.5 respectively) and Week 12 (-1.7, -1.3 respectively) similar to that of EA. Participants in both EA and SA groups reported few minor adverse events.
INTERPRETATIONS
Compared to usual care, EA produced clinically important and durable improvement in arthralgia related to AIs in breast cancer patients, and SA had a similar effect. Both EA and SA were safe.
背景
关节痛是接受芳香化酶抑制剂(AIs)治疗的乳腺癌患者常见且使人虚弱的副作用,常导致药物提前停药。
方法
我们对因 AIs 而出现关节痛并报告该症状的绝经后乳腺癌女性患者进行了电针(EA)与候补对照(WLC)和假针刺(SA)的随机对照试验。针灸师使用带有 TENS 单元的 2 Hz 电刺激的手动协议对患者进行 10 次 EA/SA 治疗。针灸师使用 Streitberger(非穿透)针在非传统穴位进行 SA,而不进行电刺激。主要终点是第 8 周时 EA 和 WLC 之间的Brief Pain Inventory(BPI)疼痛严重程度;第 12 周的反应持久性和 EA 与 SA 的比较是次要目标。
结果
在 67 名随机分配的患者中,第 8 周时 EA 组的疼痛严重程度较 WLC 组降低更多(-2.2 对-0.2,p=0.0004),第 12 周时也降低更多(-2.4 对-0.2,p<0.0001)。第 8 周(-2.0 对 0.2,p=0.0006)和第 12 周(-2.1 对-0.1,p=0.0034)时,BPI 测量的疼痛相关干扰也在 EA 组得到改善,而 WLC 组则没有。第 8 周和第 12 周时,SA 引起的疼痛严重程度和疼痛相关干扰的变化幅度与 EA 相似(分别为-2.3 和-1.5,-1.7 和-1.3)。EA 和 SA 组的参与者均报告了少数轻微不良事件。
解释
与常规护理相比,EA 可显著改善乳腺癌患者因 AIs 引起的关节痛,且效果持久,SA 也具有类似效果。EA 和 SA 均安全。
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