Medical Cannabis Guidelines: Evidence-Based Recommendations
Primary Recommendation
Cannabis and cannabinoids should NOT be used as cancer-directed treatment outside of clinical trials, and evidence supports only limited medical indications: specifically, refractory chemotherapy-induced nausea/vomiting when added to standard antiemetics. 1
Established Medical Uses
Refractory Chemotherapy-Induced Nausea and Vomiting (CINV)
- Synthetic cannabinoids (dronabinol, nabilone) may be used as salvage antiemetics when standard guideline-concordant regimens fail for moderate to highly emetogenic chemotherapy 1
- Dosing for dronabinol: Start 2.5 mg orally three times daily, up-titrate to maximum 10 mg three to four times daily 1
- Dosing for nabilone: Start 1 mg orally twice daily, up-titrate to maximum 2 mg four times daily 1
- No renal or hepatic dose adjustments required 1
Other Potential Medical Applications
- Pain management: Small to modest benefits in chronic pain, though evidence quality is low 2, 3
- Muscle spasticity: Particularly in multiple sclerosis, with modest benefits 2, 3
- Refractory epilepsy: CBD specifically shows benefit 2, 3
- Appetite stimulation: Limited supporting data 3
What NOT to Use Cannabis For
Do not recommend cannabis/cannabinoids for:
- Cancer treatment itself (no antineoplastic effect demonstrated) 1
- High-dose CBD (≥300 mg/day) for symptom management due to lack of efficacy and risk of reversible liver enzyme abnormalities 1
- Most other cancer-related symptoms outside clinical trials - evidence is insufficient 1
- Quality of life improvement - no significant benefit demonstrated 1
Clinical Communication Framework
Routine Assessment Required
Clinicians must routinely and nonjudgmentally inquire about cannabis use given 20-40% of cancer patients report use 1
Essential history elements to document: 1
- Current and prior cannabis use patterns
- Product types and THC:CBD ratios
- Route of administration (inhaled, oral, transdermal)
- Source (medical dispensary vs. informal)
- Perceived effectiveness and side effects
- Goals of use
Language Matters
- Avoid stigmatizing terms like "user" or "addict" 1
- Use patient's preferred terminology 1
- Remain sensitive to disproportionate legal impacts on marginalized communities 1
Pharmacokinetics: Critical Dosing Considerations
Route-Dependent Absorption
- Oral THC: 4-12% bioavailability, onset 30 minutes to 2 hours, duration 5-8 hours 1
- Inhaled THC: 10-35% bioavailability, onset seconds to minutes, duration 2-3 hours 1
- High-fat meals significantly increase oral absorption - warn patients about enhanced effects 1
Start Low, Go Slow Approach
Critical dosing principle: Begin at lowest possible dose and titrate slowly to avoid adverse effects 1
- Patients unfamiliar with oral products must wait ≥1 hour before additional dosing 1
- Stacking doses (taking more before onset) commonly causes adverse effects 1
Safety Considerations and Adverse Effects
Common Adverse Effects
Expect these dose-limiting side effects: 1
- Euphoria and drowsiness
- Dizziness and vertigo
- Hallucinations and mood changes
- Sedation (19% in clinical trials)
- Disorientation (3%)
Serious Safety Concerns
Driving and safety-sensitive work: 1
- Avoid driving for up to 12 hours after cannabis consumption
- Risk of motor vehicle accidents more than doubles 1
- Applies to operating heavy equipment and working with vulnerable populations
Drug interactions: 1
- Warfarin, buprenorphine, tacrolimus require monitoring
- Concurrent opioid use increases pharmacodynamic interaction risk
- May exacerbate psychotic disorders
Contraindications and cautions: 1
- History of substance use disorder predisposes to cannabis use disorder
- Adolescents and young adults at higher risk for adverse outcomes 2
- Pregnancy concerns: prematurity and restricted fetal growth 2
Storage Safety
Prevent accidental exposure: 1
- Store in locked location, out of reach of children and pets
- Keep separate from regular food/drinks
- Use child-resistant packaging
- Edibles (baked goods, candies) pose highest accidental ingestion risk
Product Quality and Sourcing
Favor formally sourced products from medical dispensaries over informal sources 1
- Dispensary products undergo testing for cannabinoid concentrations
- Screened for heavy metals and contaminants
- Labeled with THC:CBD ratios
Evidence Quality Assessment
The evidence base is weak: 1
- Most outcomes have low or very low certainty evidence
- Limited high-quality RCTs available
- Most research focuses on THC; minimal CBD data
- Results show varying and conflicting effects
Critical research gap: Cannabis access has outpaced supporting science 1
When to Refer
Refer to medical cannabis specialist if: 1
- Clinician lacks knowledge/training in medical cannabis
- Uncomfortable discussing the topic
- Complex patient requiring specialized guidance
- Maintain ongoing communication with specialists to ensure safe use
Legal Context
Federal vs. state law conflict: 1
- Cannabis remains Schedule I federally (no accepted medical use)
- 38 states have legalized medical cannabis
- Discuss local regulations with patients to avoid legal consequences 1