Department of Clinical and Molecular Medicine, Faculty of Medicine and Health Sciences, NTNU Norwegian University of Science and Technology, Postbox 8905, N-7491, Trondheim, Norway.
Cancer Clinic, St. Olavs Hospital, Trondheim University Hospital, Trondheim, Norway.
Support Care Cancer. 2021 Apr;29(4):2047-2055. doi: 10.1007/s00520-020-05693-6. Epub 2020 Aug 27.
Although corticosteroids are frequently used in patients with advanced cancer, few studies have examined the impact of these drugs on patient-reported sleep. We aimed to examine the short-term impact of methylprednisolone on patient-reported sleep in patients with advanced cancer.
Patient-reported sleep was a predefined secondary outcome in a prospective, randomized, placebo-controlled, double-blind trial that evaluated the analgesic efficacy of corticosteroids in advanced cancer patients (18+), using opioids, and having pain ≥ 4 past 24 h (NRS 0-10). Patients were randomized to the methylprednisolone group with methylprednisolone 16 mg × 2/day or placebo for 7 days. The EORTC QLQ-C30 (0-100) and the Pittsburgh Sleep Quality Index questionnaire (PSQI) (0-21) were used to assess the impact of corticosteroids on sleep at baseline and at day 7.
Fifty patients were randomized of which 25 were analyzed in the intervention group and 22 in the control group. Mean age was 64 years, mean Karnofsky performance status was 67 (SD 13.3), 51% were female, and the mean oral daily morphine equivalent dose was 223 mg (SD 222.77). Mean QLQ-C30 sleep score at baseline was 29.0 (SD 36.7) in the methylprednisolone group and 24.2 (SD 27.6) in the placebo group. At day 7, there was no difference between the groups on QLQ-C30 sleep score (methylprednisolone 20.3 (SD 32.9); placebo 28.8 (SD 33.0), p = 0.173). PSQI showed similar results.
Methylprednisolone 16 mg twice daily for 7 days had no impact on patient-reported sleep in this cohort of patients with advanced cancer.
Clinical trial information NCT00676936 (13.05.2008).
尽管皮质类固醇经常用于晚期癌症患者,但很少有研究探讨这些药物对患者报告睡眠的影响。我们旨在研究甲基强的松龙对晚期癌症患者患者报告睡眠的短期影响。
患者报告睡眠是一项前瞻性、随机、安慰剂对照、双盲试验的预先设定的次要结局,该试验评估了皮质类固醇在使用阿片类药物且疼痛≥4/24 小时(NRS 0-10)的晚期癌症患者中的镇痛疗效。患者被随机分为甲基强的松龙组,每天接受甲基强的松龙 16mg×2 次或安慰剂治疗 7 天。EORTC QLQ-C30(0-100)和匹兹堡睡眠质量指数问卷(PSQI)(0-21)用于评估皮质类固醇对基线和第 7 天睡眠的影响。
50 名患者被随机分组,其中 25 名患者被纳入干预组,22 名患者被纳入对照组。平均年龄为 64 岁,平均卡诺夫斯基表现状态为 67(SD 13.3),51%为女性,口服每日吗啡当量剂量平均为 223mg(SD 222.77)。甲基强的松龙组基线时 QLQ-C30 睡眠评分平均为 29.0(SD 36.7),安慰剂组为 24.2(SD 27.6)。第 7 天,两组间 QLQ-C30 睡眠评分无差异(甲基强的松龙 20.3(SD 32.9);安慰剂 28.8(SD 33.0),p=0.173)。PSQI 也显示出相似的结果。
在这组晚期癌症患者中,每天两次服用甲基强的松龙 16mg 持续 7 天对患者报告的睡眠没有影响。
临床试验信息 NCT00676936(2008 年 5 月 13 日)。