Oral Cannabis Extract for Secondary Prevention of Chemotherapy-Induced Nausea and Vomiting: Final Results of a Randomized, Placebo-Controlled, Phase II/III Trial

Author(s): Peter Grimison, PhD, MPH, MBBS, BSc, FRACP1,2; Antony Mersiades, MBBS2,3; Adrienne Kirby, MSc, BSc (Hons I)2; Annette Tognela, MBBS4; Ian Olver, MD, PhD, AM5; Rachael L. Morton, PhD, MScMed(Clin Epi)(Hons)2; Paul Haber, PhD, MBBS, BMedSci, FAChAM6; Anna Walsh, BPharmForenSc2; Yvonne Lee, PhD2; Ehtesham Abdi, MBBS (Adel), AFRACMA, FRACP, FACP7; Stephen Della-Fiorentina, OAM, MBBS (Hons), FRACP8; Morteza Aghmesheh, MD, PhD9; Peter Fox, MBBS10; Karen Briscoe, MBBS11; Jasotha Sanmugarajah, MBBS12; Gavin Marx, MBBS13; Ganessan Kichenadasse, MBBS14; Helen Wheeler, MBBS15; Matthew Chan, MBBS16; Jenny Shannon, MBBS17; Craig Gedye, MBBS18; Stephen Begbie, MBBS19; R. John Simes, MD, PhD2; Martin R. Stockler, MBBS2
Source: https://doi.org/10.1200/JCO.23.01836

Dr. Maen Hussein's Thoughts

THC helped, but had more adverse events, (sedation, dizziness, etc.) THC was in addition to other prophylactic antiemetic, improved response rate from 8 to 24%.

PURPOSE

The aim of this randomized, placebo-controlled, two-stage, phase II/III trial was to determine the efficacy of an oral cannabis extract in adults with refractory nausea and/or vomiting during moderately or highly emetogenic, intravenous chemotherapy despite guideline-consistent antiemetic prophylaxis. Here, we report results of the prespecified combined analysis including the initial phase II and subsequent phase III components.

PATIENTS AND METHODS

Study treatment consisted of oral capsules containing either tetrahydrocannabinol 2.5 mg plus cannabidiol 2.5 mg capsules (THC:CBD) or matching placebo, taken three times a day from days –1 to 5, in addition to guideline-consistent antiemetics. The primary measure of effect was the difference in the proportions of participants with no vomiting or retching and no use of rescue medications (a complete response) during hours 0-120 after the first cycle of chemotherapy on study (cycle A).

RESULTS

We recruited 147 evaluable of a planned 250 participants from 2016 to 2022. Background antiemetic prophylaxis included a corticosteroid and 5-hydroxytryptamine antagonist in 97%, a neurokinin-1 antagonist in 80%, and olanzapine in 10%. THC:CBD compared with placebo improved the complete response rate from 8% to 24% (absolute difference 16%, 95% CI, 4 to 28, P = .01), with similar effects for absence of significant nausea, use of rescue medications, daily vomits, and the nausea scale on the Functional Living Index—Emesis quality-of-life questionnaire. More frequent bothersome adverse events of special interest included sedation (18% v 7%), dizziness (10% v 0%), and transient anxiety (4% v 1%). There were no serious adverse events attributed to THC:CBD.

CONCLUSION

THC:CBD is an effective adjunct for chemotherapy-induced nausea and vomiting despite standard antiemetic prophylaxis, but was associated with additional adverse events. Drug availability, cultural attitudes, legal status, and preferences may affect implementation. Future analyses will evaluate the cost-effectiveness of THC:CBD.

Author Affiliations

1Chris O’Brien Lifehouse, Sydney, NSW, Australia; 2NHMRC Clinical Trials Centre, University of Sydney, Sydney, NSW, Australia; 3Dept of Medical Oncology, Northern Beaches Hospital, Frenchs Forest, NSW, Australia; 4Macarthur Cancer Therapy Centre, Campbelltown Hospital, Campbelltown, NSW, Australia; 5University of Adelaide, Adelaide, SA, Australia; 6Royal Prince Alfred Hospital, Sydney, NSW, Australia; 7The Tweed Hospital, Tweed Heads, NSW, Australia; 8Southern Highlands Cancer Centre, Bowral, NSW, Australia; 9Department of Medical Oncology, Wollongong Hospital, Wollongong, NSW, Australia; 10Dept of Medical Oncology, Orange Base Hospital, Orange, NSW, Australia; 11Department of Medical Oncology, Coffs Harbour Hospital, Coffs Harbour, NSW, Australia; 12Department of Medical Oncology, Gold Coast University Hospital, Gold Coast, QLD, Australia; 13Department of Medical Oncology, Sydney Adventist Hospital, Wahroonga, NSW, Australia; 14Department of Medical Oncology, Flinders Medical Centre, Adelaide, NSW, Australia; 15Department of Medical Oncology, Royal North Shore Hospital, Gosford, NSW, Australia; 16Department of Medical Oncology, Gosford Hospital, Gosford, NSW, Australia; 17Department of Medical Oncology, Nepean Hospital, Kingswood, NSW, Australia; 18Department of Medical Oncology, Calvary Mater Hospital, Newcastle, NSW, Australia; 19Department of Medical Oncology, Port Macquarie Hospital, Port Macquarie, NSW, Australia;

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