Dupilumab (Dupixent): Uses and Applications
Dupilumab (Dupixent) is primarily used for the treatment of moderate-to-severe atopic dermatitis in adults and children who have not achieved adequate control with topical medications. 1
Primary Indications
Atopic Dermatitis
- FDA-approved for moderate-to-severe atopic dermatitis in adults and adolescents
- Approved for severe atopic dermatitis in children aged 6-11 years 2
- Administered as subcutaneous injections with an initial loading dose followed by maintenance dosing:
- Adults: 600 mg loading dose, then 300 mg every 2 weeks 1
- Pediatric dosing varies by age and weight
Secondary Indications
- Moderate-to-severe uncontrolled asthma (as add-on maintenance therapy) 3
- Dyshidrotic eczema (off-label use with promising results) 4
Mechanism of Action
Dupilumab is a fully human monoclonal antibody that:
- Blocks both interleukin-4 and interleukin-13 signaling by targeting the IL-4 receptor α
- Inhibits key inflammatory pathways involved in type 2 inflammation
Efficacy
- Long-term studies show sustained efficacy for up to 5 years in adults with atopic dermatitis 5
- At week 260 of long-term treatment:
- 67.5% of patients achieved clear or almost clear skin (IGA score 0-1)
- 88.9% achieved at least 75% improvement in EASI scores 5
Safety Profile and Side Effects
Common Side Effects
- Conjunctivitis (15.6% in real-world studies) 2
- Head and neck dermatitis (19.5%) 2
- Nasopharyngitis
- Upper respiratory tract infections
- Injection site reactions
Ocular Side Effects Management
The British Association of Dermatologists provides specific guidance for managing dupilumab-related ocular surface disorders (DROSD):
Pre-treatment Assessment:
- Offer prophylactic preservative-free ocular lubricants to patients with current or pre-existing corneal or conjunctival eye disease 1
- Refer patients with significant current or chronic eye disease to ophthalmology before starting treatment 1
- Delay dupilumab therapy for patients with corneal transplant until ophthalmology consultation 1
During Treatment Monitoring:
Long-term Safety
- Exposure-adjusted rates of treatment-emergent adverse events generally remain stable or decline over time 5
- Most side effects are mild and do not require discontinuation of therapy 2
- No significant safety signals have emerged in 5-year extension studies 5
Clinical Considerations
- No laboratory monitoring is required before initiation or during treatment 1
- Conjunctivitis is a common adverse event but is typically self-limited and can be managed with artificial tears 1
- Ophthalmology referral should be considered for severe, persistent, or refractory conjunctivitis 1
- Risk factors for developing ocular complications include:
- Previous ophthalmology attendance for ocular surface disorders
- Higher baseline disease severity
- Eyelid or facial eczema 1
Dupilumab represents a significant advancement in the treatment of moderate-to-severe atopic dermatitis with a favorable long-term safety profile, making it an important option for patients who have failed conventional topical therapies.