Lee Jee Young, Oh Hye Kyung, Ryu Han Sung, Yoon Sung Soo, Eo Wankyu, Yoon Seong Woo
1 Korean Medicine Cancer Center, Kyung Hee University Hospital at Gangdong, Seoul, Republic of Korea.
2 College of Medicine, Kyung Hee University, Seoul, Republic of Korea.
Integr Cancer Ther. 2018 Jun;17(2):524-530. doi: 10.1177/1534735417734914. Epub 2017 Oct 16.
Sleep disturbance is the second most bothersome symptom in patients with cancer, and it can significantly impair their quality of life. The aim of this study was to investigate the efficacy and safety of the traditional herbal medicine Gamiguibi-tang (GGBT) in patients with cancer-related sleep disturbance.
We conducted a prospective, randomized, wait-list-controlled, open-label pilot clinical trial on cancer-related sleep disturbance. Patients with cancer experiencing poor sleep quality with a Pittsburgh Sleep Quality Index of at least 6 were randomly assigned to the GGBT and wait-list groups to receive GGBT and conventional care, respectively, for 2 weeks. The primary endpoint was the Insomnia Severity Index (ISI) score. Fatigue, depression, and cognitive impairment were assessed as the secondary endpoints by using the Brief Fatigue Inventory (BFI), Beck Depression Inventory (BDI), and Montreal Cognitive Assessment (MoCA).
Thirty participants who met the eligibility criteria were enrolled. Sleep disturbance assessed using the ISI improved significantly more in the GGBT group than in the wait-list group (-5.5 ± 4.4 vs 0.1 ± 1.1, P < .001). Fatigue level determined using the BFI also improved significantly more in the GGBT group than in the wait-list group (-0.8 ± 0.8 vs 0.0 ± 0.3, P = .002). The BDI and MoCA scores showed no significant changes. Adverse events were reported in two patients in the GGBT group and consisted of mild dyspepsia and mild edema.
GGBT may be a potential treatment option for cancer-related sleep disturbance. Further research is needed to investigate the efficacy and safety of GGBT.
睡眠障碍是癌症患者第二大困扰症状,会显著损害其生活质量。本研究旨在调查传统草药加味归脾汤(GGBT)治疗癌症相关睡眠障碍的疗效和安全性。
我们针对癌症相关睡眠障碍开展了一项前瞻性、随机、等待列表对照、开放标签的试点临床试验。匹兹堡睡眠质量指数至少为6分、睡眠质量差的癌症患者被随机分为GGBT组和等待列表组,分别接受GGBT和常规护理,为期2周。主要终点是失眠严重程度指数(ISI)评分。采用简明疲劳量表(BFI)、贝克抑郁量表(BDI)和蒙特利尔认知评估量表(MoCA)评估疲劳、抑郁和认知障碍作为次要终点。
30名符合入选标准者入组。GGBT组使用ISI评估的睡眠障碍改善程度显著高于等待列表组(-5.5±4.4 vs 0.1±1.1,P<.001)。GGBT组使用BFI测定的疲劳水平改善程度也显著高于等待列表组(-0.8±0.8 vs 0.0±0.3,P=.002)。BDI和MoCA评分无显著变化。GGBT组有2例患者报告了不良事件,包括轻度消化不良和轻度水肿。
GGBT可能是癌症相关睡眠障碍的一种潜在治疗选择。需要进一步研究以调查GGBT的疗效和安全性。