How to Prescribe Secukinumab (Cosentyx UnoReady)
Prescribe secukinumab 300 mg subcutaneously at weeks 0,1,2,3, and 4, followed by 300 mg every 4 weeks indefinitely for moderate-to-severe plaque psoriasis, active psoriatic arthritis (with coexistent moderate-to-severe psoriasis), or active ankylosing spondylitis after completing mandatory pre-treatment screening for tuberculosis, active infections, and hepatitis B. 1, 2
Pre-Treatment Screening Requirements (Mandatory Before First Dose)
- Screen for active and latent tuberculosis using tuberculin skin test or interferon-gamma release assay; do not initiate secukinumab in patients with active TB. 1, 2
- Initiate anti-tuberculosis therapy before starting secukinumab in patients with latent TB infection. 1, 2
- Screen for active infections or sepsis; defer therapy until resolved, and consult infectious disease specialists if considering initiation during active infection. 1
- Screen for hepatitis B infection; untreated hepatitis B is a relative contraindication. 1
- Assess history of inflammatory bowel disease (IBD); secukinumab may trigger or exacerbate IBD and should be avoided in patients with active or prior IBD. 1, 3
- Complete all age-appropriate killed vaccines before initiating therapy; live attenuated vaccines must be administered at least 2-4 weeks before starting secukinumab and are absolutely contraindicated once therapy begins. 1, 2
- Administer pneumococcal vaccine and ensure annual influenza vaccination is up to date before starting therapy. 1
Dosing Regimens by Indication
Moderate-to-Severe Plaque Psoriasis (Adults)
- Administer 300 mg subcutaneously at weeks 0,1,2,3, and 4 (loading phase), then 300 mg every 4 weeks starting at week 8 (maintenance phase). 1, 2
- Each 300 mg dose is given as one 300 mg injection or two 150 mg injections. 2
- The 300 mg dose is superior to 150 mg, achieving 79% PASI 90 response at week 16 versus lower rates with 150 mg. 1, 4
- For some patients, 150 mg may be acceptable, but 300 mg should be prioritized for optimal efficacy. 2
Psoriatic Arthritis (Adults)
- For patients with PsA and coexistent moderate-to-severe plaque psoriasis, use the 300 mg dosing regimen described above for plaque psoriasis. 2
- For other adult patients with PsA, administer 150 mg at weeks 0,1,2,3, and 4, then 150 mg every 4 weeks. 2
- If active PsA persists despite 150 mg dosing, escalate to 300 mg every 4 weeks. 2
- Secukinumab may be administered with or without methotrexate. 2
Ankylosing Spondylitis (Adults)
- Administer 150 mg at weeks 0,1,2,3, and 4, then 150 mg every 4 weeks. 2
- If active AS persists, escalate to 300 mg every 4 weeks. 2
- Alternatively, initiate at 150 mg every 4 weeks without a loading phase. 2
Pediatric Plaque Psoriasis (≥6 Years)
- For patients <50 kg: administer 75 mg at weeks 0,1,2,3, and 4, then 75 mg every 4 weeks. 2
- For patients ≥50 kg: administer 150 mg at weeks 0,1,2,3, and 4, then 150 mg every 4 weeks. 2
Juvenile Psoriatic Arthritis (≥2 Years)
- For patients ≥15 kg and <50 kg: administer 75 mg at weeks 0,1,2,3, and 4, then 75 mg every 4 weeks. 2
- For patients ≥50 kg: administer 150 mg at weeks 0,1,2,3, and 4, then 150 mg every 4 weeks. 2
Administration Technique
- Inject subcutaneously in the upper arms, thighs, or any abdominal quadrant; rotate injection sites with each dose. 1, 2
- Avoid injecting into areas with active psoriasis lesions, or skin that is tender, bruised, erythematous, or indurated. 1, 2
- Adult patients may self-administer after proper training; pediatric patients should not self-administer. 2
- Upper outer arm injections must be performed by a caregiver or healthcare provider. 2
Duration of Therapy and Response Assessment
- Continue maintenance dosing every 4 weeks indefinitely without a predetermined stopping point. 1
- Assess response at week 16; discontinue if no clinical response is achieved by this timepoint. 1
- Response is sustained through at least 52 weeks and can be maintained for 2-5 years with continuous dosing. 1, 5
- Do not extend the dosing interval to every 6 weeks, even in patients achieving early PASI 90 responses; this significantly reduces efficacy. 1
- Do not use "as-needed" or intermittent dosing after the loading phase; continuous every-4-week dosing is essential. 1
Safety Monitoring During Therapy
- Monitor for mucocutaneous candida infections (1.9 events per 100 patient-years); these are typically mild and respond to standard antifungal treatment without requiring discontinuation. 1
- Monitor for serious infections (0.015 events per patient-year); temporarily discontinue secukinumab until infection resolves. 1
- Watch for new-onset or worsening inflammatory bowel disease; immediately discontinue secukinumab if IBD develops or worsens. 1
- Neutropenia may occur but is usually mild, transient, and reversible. 1
- Development of neutralizing antibodies occurs in <1% of patients and rarely impacts efficacy. 1
Combination Therapy Considerations
- Combination with high-potency topical corticosteroids with or without vitamin D analogues may augment efficacy, though published safety data on combinations is limited. 1
- Do not combine secukinumab with other biologics; such combinations carry unknown risks. 1
- Secukinumab is recommended as monotherapy for all approved indications. 1
Patient Selection Considerations
- Secukinumab is the preferred first-line biologic for moderate-to-severe plaque psoriasis without psoriatic arthritis, achieving superior PASI 90 response (79%) compared to ustekinumab (57.6%) at week 16. 4
- For patients with concurrent psoriatic arthritis, consider ustekinumab as first-line if musculoskeletal disease is the primary concern. 4
- For patients with a history of inflammatory bowel disease, choose ustekinumab instead of secukinumab due to the risk of IBD exacerbation with IL-17A inhibition. 4, 3
- Secukinumab is strongly recommended for moderate-to-severe nail involvement, palmoplantar plaque psoriasis, and psoriasis with psoriatic arthritis. 1
Common Pitfalls to Avoid
- Do not use the 150 mg dose when 300 mg is appropriate for plaque psoriasis; the higher dose provides markedly greater efficacy with comparable safety. 1
- Do not delay treatment for killed vaccines; these can be administered after starting therapy, but live vaccines must be given before initiation. 1
- Do not initiate therapy during active infection without infectious disease consultation. 1
- Do not continue therapy beyond 16 weeks if no response is observed; consider switching to an alternative biologic. 6, 1