Systematic review and meta-analysis of cannabinoids in palliative medicine

被引:87
作者
Muecke, Martin [1 ,2 ,3 ]
Weier, Megan [4 ,5 ]
Carter, Christopher [1 ]
Copeland, Jan [4 ]
Degenhardt, Louisa [4 ]
Cuhls, Henning [1 ]
Radbruch, Lukas [1 ,6 ]
Haeuser, Winfried [7 ]
Conrad, Rupert [8 ]
机构
[1] Univ Hosp Bonn, Dept Palliat Med, Bonn, Germany
[2] Univ Hosp Bonn, Ctr Rare Dis Bonn ZSEB, Bonn, Germany
[3] Univ Hosp Bonn, Dept Gen Practice & Family Med, Bonn, Germany
[4] Univ New South Wales, Natl Drug & Alcohol Res Ctr, Sydney, NSW, Australia
[5] Univ Queensland, Ctr Youth Substance Abuse Res, Brisbane, Qld, Australia
[6] Malteser Hosp Bonn Rhein Sieg, Ctr Palliat Care, Bonn, Germany
[7] Tech Univ Munich, Dept Psychosomat Med & Psychotherapy, Munich, Germany
[8] Univ Hosp Bonn, Dept Psychosomat Med & Psychotherapy, Bonn, Germany
基金
澳大利亚国家健康与医学研究理事会;
关键词
cannabinoids; marijuana; palliation; cancer; HIV; weight gain; systematic review; CANCER-PATIENTS; CARE RESEARCH; DOUBLE-BLIND; COMBINATION THERAPY; MEGESTROL-ACETATE; MARIJUANA SMOKERS; CALORIC-INTAKE; CHRONIC PAIN; OF-LIFE; DRONABINOL;
D O I
10.1002/jcsm.12273
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
We provide a systematic review and meta-analysis on the efficacy, tolerability, and safety of cannabinoids in palliative medicine. The Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE, PsycINFO, PubMed, Scopus, and , and a selection of cancer journals were searched up until 15th of March 2017. Of the 108 screened studies, nine studies with a total of 1561 participants were included. Overall, the nine studies were at moderate risk of bias. The quality of evidence comparing cannabinoids with placebo was rated according to Grading of Recommendations Assessment, Development, and Evaluation as low or very low because of indirectness, imprecision, and potential reporting bias. In cancer patients, there were no significant differences between cannabinoids and placebo for improving caloric intake (standardized mean differences [SMD]: 0.2 95% confidence interval [CI]: [-0.66, 1.06] P=0.65), appetite (SMD: 0.81 95% CI: [-1.14, 2.75]; P=0.42), nausea/vomiting (SMD: 0.21 [-0.10, 0.52] P=0.19), >30% decrease in pain (risk differences [RD]: 0.07 95% CI: [-0.01, 0.16]; P=0.07), or sleep problems (SMD: -0.09 95% CI: [-0.62, 0.43] P=0.72). In human immunodeficiency virus (HIV) patients, cannabinoids were superior to placebo for weight gain (SMD: 0.57 [0.22; 0.92]; P=0.001) and appetite (SMD: 0.57 [0.11; 1.03]; P=0.02) but not for nausea/vomiting (SMD: 0.20 [-0.15, 0.54]; P=0.26). Regarding side effects in cancer patients, there were no differences between cannabinoids and placebo in symptoms of dizziness (RD: 0.03 [-0.02; 0.08]; P=0.23) or poor mental health (RD: -0.01 [-0.04; 0.03]; P=0.69), whereas in HIV patients, there was a significant increase in mental health symptoms (RD: 0.05 [0.00; 0.11]; P=0.05). Tolerability (measured by the number of withdrawals because of adverse events) did not differ significantly in cancer (RD: 1.15 [0.80; 1.66]; P=0.46) and HIV patients (RD: 1.87 [0.60; 5.84]; P=0.28). Safety did not differ in cancer (RD: 1.12 [0.86; 1.46]; P=0.39) or HIV patients (4.51 [0.54; 37.45]; P=0.32) although there was large uncertainty about the latter reflected in the width of the CI. In one moderate quality study of 469 cancer patients with cancer-associated anorexia, megestrol was superior to cannabinoids in improving appetite, producing >10% weight gain and tolerability. In another study comparing megestrol to dronabinol in HIV patients, megestrol treatment led to higher weight gain without any differences in tolerability and safety. We found no convincing, unbiased, high quality evidence suggesting that cannabinoids are of value for anorexia or cachexia in cancer or HIV patients.
引用
收藏
页码:220 / 234
页数:15
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