Study register · detail
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
Share
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.