Cancer
Study register · detail Systematische Review + Meta-Analyse · Cancer · 2020

Cannabinoids for adult cancer-related pain: systematic review and meta-analysis

No benefit demonstrated GRADE High 134 citations
Samplek = 5 Studien
n = 1.442 Pat.
Durationunclear
ControlPlacebo or other active comparators
EndpointNRS
Blindingdoppelblind
DesignSystematische Review + Meta-Analyse
Key finding

Cannabinoids showed no significant difference from placebo in pain relief (Numeric Rating Scale), but an increased risk of adverse effects such as somnolence and dizziness.

Summary

Systematic review with meta-analysis on cannabinoids in cancer-associated pain; k=5 RCTs (n=1442, all low risk of bias). No difference between cannabinoids+opioids vs. placebo+opioids in average NRS pain reduction (MD -0,21 [95% CI -0,48 to 0,07], p=0,14); phase III subanalysis: MD -0,02 (95% CI -0,21 to 0,16, p=0,80). Cannabinoids with higher risk of somnolence (OR 2,69 [95% CI 1,54–4,71], p<0,001) and dizziness (OR 1,58 [95% CI 0,99–2,51], p=0,05); no treatment-associated deaths.

P
PopulationAdults with cancer-related pain, pooled n=1460
I
InterventionCannabinoids (various) as add-on to opioids
C
ControlPlacebo or other active comparators
O
OutcomeNo significant difference in NRS pain reduction (MD -0,21; 95% CI -0,48 to 0,07; p=0,14); increased risk of somnolence (OR 2,69; p<0,001) and dizziness (OR 1,58; p=0,05)
Confidence in the evidence
High

The highest of four GRADE levels, the effect estimate is very reliable.

Quality profile
Sample size
Blinding Double-blind
Effect size No benefit
Citations / year
Authors
Boland EG, Bennett MI, Allgar V, Boland JW
DOI 10.1136/bmjspcare-2019-002032
Design: Systematische Review + Meta-Analyse
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Abstract
Objectives: There is increased interest in cannabinoids for cancer pain management and legislative changes are in progress in many countries. This study aims to determine the beneficial and adverse effects of cannabis/cannabinoids compared with placebo/other active agents for the treatment of cancer-related pain in adults. Methods: Systematic review and meta-analysis to identify randomised controlled trials of cannabinoids compared with placebo/other active agents for the treatment of cancer-related pain in adults to determine the effect on pain intensity (primary outcome) and adverse effects, including dropouts. Searches included Embase, MEDLINE, PsycINFO, Web of Science, ClinicalTrials.gov, Cochrane and grey literature. Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines were followed. Results: We identified 2805 unique records, of which six randomised controlled trials were included in this systematic review (n=1460 participants). Five studies were included in the meta-analysis (1442 participants). All had a low risk of bias. There was no difference between cannabinoids and placebo for the difference in the change in average Numeric Rating Scale pain scores (mean difference -0.21 (-0.48 to 0.07, p=0.14)); this remained when only phase III studies were meta-analysed: mean difference -0.02 (-0.21 to 0.16, p=0.80). Cannabinoids had a higher risk of adverse events when compared with placebo, especially somnolence (OR 2.69 (1.54 to 4.71), p<0.001) and dizziness (OR 1.58 (0.99 to 2.51), p=0.05). No treatment-related deaths were reported. Dropouts and mortality rates were high. Conclusions: Studies with a low risk of bias showed that for adults with advanced cancer, the addition of cannabinoids to opioids did not reduce cancer pain. Trial Registration Number: CRD42018107662.

The impediment to action advances action. — Marcus Aurelius