Study register · detail
Clear benefit
GRADE
Moderate
50 citations
Samplen = 28 Pat.
EndpointAntiemetic response
Blindingn.a.
DesignOffene Dosisfindungsstudie
Cannabinoidthc
Max. dose1.5 mg
Key finding
Intramuscular levonantradol achieved an antiemetic effect in 89 % of patients at low doses starting from 0,5 mg.
Summary
n=28 cancer patients undergoing chemotherapy, refractory to standard antiemetics, IM levonantradol 0,5–1,5 mg; response rate 89% (25/28) complete or partial; dysphoria as dose-limiting toxicity in 16% (5/31 evaluable patients); somnolence 48%, dry mouth 32%.
P
PopulationCancer patients undergoing chemotherapy, refractory to conventional antiemetic therapy, n=28 (antiemetic response) / n=31 (toxicity)
I
InterventionIntramuscular levonantradol (synthetic THC derivative), starting dose 0,5 mg, escalation in 0,5-mg steps up to max. 1,5 mg
O
Outcome89 % (25/28) of patients achieved a complete or partial antiemetic response at doses of 0,5–1,5 mg; dose-limiting toxicity (dysphoria) in 16 % (5/31) at 1,0–1,5 mg
Confidence in the evidence
Moderate
The third of four GRADE levels, the effect estimate is probably reliable.
Downgraded for
Imprecision
Quality profile
Sample size
★★★★★
Blinding
—
Effect size
Clear benefit
Citations / year
★★★★★
Authors
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Abstract
Positive results of investigations of the antiemetic activity of delta-9-tetrahydrocannabinol (THC) in patients receiving cancer chemotherapy have led to the development of levonantradol, a synthetic derivative of THC. We assessed both the antiemetic activity and toxicity of intramuscular levonantradol in patients receiving cancer chemotherapy who were refractory to conventional antiemetic therapy. An open dose-finding study was conducted using initial doses of 0.5 mg. Doses were escalated by 0.5 mg when an incomplete response with no toxicity was observed. Of the 28 patients initially treated, 25/28 (89 per cent) achieved a complete or partial antiemetic response at doses ranging from 0.5 to 1.5 mg. There was no difference in response rate with respect to age or patient size. Of the 31 patients evaluable for toxicity, six reported none. Dysphoria, the dose-limiting toxicity, occurred in five patients (16 per cent) at 1.0 to 1.5-mg doses. The most commonly reported side effects were somnolence (48 per cent) and dry mouth (32 per cent). We conclude that intramuscular levonantradol is an effective antiemetic at doses as low as 0.5 mg.
The impediment to action advances action.