Hunter Catherine N, Abdel-Aal Hesham H, Elsherief Wessam A, Farag Dina E, Riad Nermine M, Alsirafy Samy A
Palliative Medicine Unit, Kasr Al-Ainy Center of Clinical Oncology and Nuclear Medicine, Kasr Al-Ainy School of Medicine, Cairo University, Cairo, Egypt.
Clinical and Chemical Pathology Department, Kasr Al-Ainy School of Medicine, Cairo University, Cairo, Egypt.
J Pain Symptom Manage. 2021 Dec;62(6):1207-1215. doi: 10.1016/j.jpainsymman.2021.05.017. Epub 2021 May 26.
Few pharmacological interventions are available for cancer-associated anorexia and cachexia. Mirtazapine has been suggested for use in cancer-associated anorexia and cachexia.
This study was conducted to assess the efficacy and tolerability of mirtazapine in cancer-associated anorexia and cachexia.
A double-blind placebo-controlled randomized trial. The study included 120 incurable solid tumour patients with anorexia (appetite loss ≥4 on 0 - 10 scale, 10 = maximum appetite loss), cachexia (>5% body weight loss over 6 months or >2% plus body mass index <20) and depression score ≤3 on 0-6 scale (6 = extreme feelings of depression). Patients were 1:1 randomized to receive mirtazapine 15mg daily at night for 8 weeks or placebo. The primary endpoint was change in appetite from baseline to day 28. Other outcomes included changes in quality-of-life, fatigue, depressive symptoms, body weight, lean body mass, handgrip strength, inflammatory markers, adverse events and survival.
48 (80%) patients in the mirtazapine arm and 52 (87%) in the placebo were assessable for the 1ry endpoint. Appetite score increased significantly with mirtazapine as well as with placebo (P < 0.0001 each). The increase in appetite score did not differ significantly between the two arms in the per-protocol and intention-to-treat analysis (P = 0.472 and 0.462, respectively). Mirtazapine was associated with significantly less increase in depressive symptoms and higher prevalence of somnolence. The change in other outcomes did not differ significantly between mirtazapine and placebo.
Mirtazapine 15mg at night for 28 days is no better than placebo in improving the appetite of incurable solid tumor patients with cancer-associated anorexia and cachexia.
针对癌症相关性厌食和恶病质,几乎没有可用的药物干预措施。米氮平已被建议用于治疗癌症相关性厌食和恶病质。
本研究旨在评估米氮平治疗癌症相关性厌食和恶病质的疗效及耐受性。
一项双盲安慰剂对照随机试验。该研究纳入了120例患有厌食(在0至10分的量表上食欲丧失≥4分,10分表示最大食欲丧失)、恶病质(6个月内体重减轻>5%或体重减轻>2%且体重指数<20)且抑郁评分在0至6分的量表上≤3分(6分表示极度抑郁情绪)的不可治愈实体瘤患者。患者按1:1随机分组,接受每晚15mg米氮平治疗8周或安慰剂治疗。主要终点是从基线到第28天食欲的变化。其他结果包括生活质量、疲劳、抑郁症状、体重、瘦体重、握力、炎症标志物、不良事件和生存率的变化。
米氮平组48例(80%)患者和安慰剂组52例(87%)患者可对主要终点进行评估。米氮平和安慰剂治疗后食欲评分均显著增加(每组P<0.0001)。在意向性分析和符合方案分析中,两组食欲评分的增加无显著差异(分别为P=0.472和0.462)。米氮平与抑郁症状的增加显著较少和嗜睡的患病率较高相关。米氮平和安慰剂在其他结果的变化上无显著差异。
每晚服用15mg米氮平持续28天,在改善患有癌症相关性厌食和恶病质的不可治愈实体瘤患者的食欲方面并不比安慰剂更好。