Eguchi Kenji, Honda Michitaka, Kataoka Tatusji, Mukouyama Taketo, Tsuneto Satoru, Sakamoto Junichi, Oba Koji, Saji Shigetoyo
Department of Oncology,Teikyo University,Tokyo,Japan.
Department of Gastroenterological Surgery,Cancer Institute, Ariake Hospital,Japanese Foundation for Cancer Research,Koto-ku,Tokyo,Japan.
Palliat Support Care. 2015 Oct;13(5):1301-8. doi: 10.1017/S1478951514001254. Epub 2014 Nov 5.
Cancer-related fatigue (CRF) is a common and one of the most important issues in palliative medicine, and it has been demonstrated to have a significant impact on patient quality of life (QoL). The present pilot randomized controlled study evaluated the efficacy and toxicity of methylprednisolone (MP) for CRF in advanced cancer patients.
Our study was planned as a randomized, double-blind, multicenter, placebo-controlled trial. Patients were randomly assigned to an MP group, who received 32 mg/day of MP orally for 7 days, and a placebo group. The primary endpoint was an improvement in visual analog scale (VAS) score for fatigue from baseline to day 7. The secondary endpoints were improvements in appetite loss and QoL as well as evaluating the safety of corticosteroids as palliative therapy.
It was not possible to complete patient registration. In total, 35 patients were randomly assigned to an MP group (n = 18) and a placebo group (n = 17). The mean changes in VAS score for fatigue were -9.06 in the placebo group and -1.56 in the MP group, and for appetite loss -6.44 in the placebo group and -8.06 in the MP group. In addition, there was no evidence that methylprednisolone improved appetite loss or QoL compared to placebo. The incidence of adverse effects was not greater in the MP group. Significant of Result: We conclude that our sample size was too small to prove the efficacy of methylprednisolone in improving fatigue. Our results were reported as a pilot study performed to support a subsequent larger trial.
癌症相关疲劳(CRF)是姑息医学中常见且最重要的问题之一,已证明其对患者生活质量(QoL)有重大影响。本初步随机对照研究评估了甲泼尼龙(MP)对晚期癌症患者CRF的疗效和毒性。
我们的研究计划为一项随机、双盲、多中心、安慰剂对照试验。患者被随机分配至MP组(口服32mg/天的MP,共7天)和安慰剂组。主要终点是从基线到第7天疲劳视觉模拟量表(VAS)评分的改善情况。次要终点是食欲减退和生活质量的改善,以及评估皮质类固醇作为姑息治疗的安全性。
无法完成患者登记。总共35名患者被随机分配至MP组(n = 18)和安慰剂组(n = 17)。安慰剂组疲劳VAS评分的平均变化为 -9.06,MP组为 -1.56;安慰剂组食欲减退的平均变化为 -6.44,MP组为 -8.06。此外,没有证据表明与安慰剂相比,甲泼尼龙能改善食欲减退或生活质量。MP组不良反应的发生率并不更高。结果的意义:我们得出结论,我们的样本量太小,无法证明甲泼尼龙在改善疲劳方面的疗效。我们的结果作为一项初步研究报告,以支持后续更大规模的试验。