Palliative Care
Study register · detail RCT · Palliative Care · 2013

An open-label extension study to investigate the long-term safety and tolerability of THC/CBD oromucosal spray and oromucosal THC spray in patients with terminal cancer-related pain refractory to strong opioid analgesics.

Clear benefit GRADE Low 231 citations
Samplen = 43 Pat.
DurationFollow-up after two-week parent…
EndpointBPI-SF
Blindingoffen
DesignRCT
Cannabinoidkombination
THC:CBD1:1
Routeoromukosal
Key finding

THC/CBD spray showed improvement in pain intensity and worst pain as well as improvement in insomnia, pain and fatigue with good tolerability over longer-term use.

Summary

Open-label extension study (n=43) following a preceding 2-week RCT on THC/CBD oromucosal spray in refractory cancer pain. Brief Pain Inventory-Short Form: improvement in 'pain severity' and 'worst pain' at every follow-up visit. EORTC QLQ-C30: improvement in the domains insomnia, pain, fatigue. No dose increase over time (no indication of tolerance development), good long-term tolerability.

P
PopulationPatients with advanced cancer and opioid-refractory tumor-related pain, n=43
I
InterventionTHC/CBD oromucosal spray (nabiximols/Sativex, n=39) or THC spray (n=4), self-titrated to symptom control or maximum dose
O
OutcomeImprovement in pain intensity (BPI-SF 'pain severity' and 'worst pain') as well as quality of life (EORTC QLQ-C30: insomnia, pain, fatigue) at every visit; no new safety concerns
Confidence in the evidence
Low

The second of four GRADE levels, the effect estimate is of limited reliability.

Downgraded for
Risk of biasImprecision
Quality profile
Sample size
Blinding Open-label
Effect size Clear benefit
Citations / year
Authors
Johnson JR, Lossignol D, Burnell-Nugent M, Fallon MT
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Abstract
Context: Chronic pain in patients with advanced cancer poses a serious clinical challenge. The Delta9-tetrahydrocannabinol (THC)/cannabidiol (CBD) oromucosal spray (U.S. Adopted Name, nabiximols; Sativex((R))) is a novel cannabinoid formulation currently undergoing investigation as an adjuvant therapy for this treatment group. Objectives: This follow-up study investigated the long-term safety and tolerability of THC/CBD spray and THC spray in relieving pain in patients with advanced cancer. Methods: In total, 43 patients with cancer-related pain experiencing inadequate analgesia despite chronic opioid dosing, who had participated in a previous three-arm (THC/CBD spray, THC spray, or placebo), two-week parent randomized controlled trial, entered this open-label, multicenter, follow-up study. Patients self-titrated THC/CBD spray (n=39) or THC spray (n=4) to symptom relief or maximum dose and were regularly reviewed for safety, tolerability, and evidence of clinical benefit. Results: The efficacy end point of change from baseline in mean Brief Pain Inventory-Short Form scores for "pain severity" and "worst pain" domains showed a decrease (i.e., improvement) at each visit in the THC/CBD spray patients. Similarly, the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-C30 scores showed a decrease (i.e., improvement) from baseline in the domains of insomnia, pain, and fatigue. No new safety concerns associated with the extended use of THC/CBD spray arose from this study. Conclusion: This study showed that the long-term use of THC/CBD spray was generally well tolerated, with no evidence of a loss of effect for the relief of cancer-related pain with long-term use. Furthermore, patients who kept using the study medication did not seek to increase their dose of this or other pain-relieving medication over time, suggesting that the adjuvant use of cannabinoids in cancer-related pain could provide useful benefit.

The impediment to action advances action. — Marcus Aurelius