Secukinumab dosing optimization in patients with moderate-to-severe plaque psoriasis: results from the randomized, open-label OPTIMISE study.
Kristian ReichL PuigJ C SzepietowskiCarle F PaulJ P LacourA TsianakasC SiederM RisslerE PournaraR OrsenigoPublished in: The British journal of dermatology (2019)
Standard q4w dosing of secukinumab 300 mg is the optimal dosing regimen to achieve and maintain clear or almost clear skin. Patients with body weight ≥ 90 kg not achieving PASI 90 at week 24 may benefit from the q2w dosing regimen. What's already known about this topic? Individual responses to biologics in patients with psoriasis vary considerably and there may be a need to individualize treatment. Dose optimization strategies of currently available biologic drugs have been investigated mainly in rheumatic disorders. Secukinumab has shown long-term PASI 90/100 responses (percentage improvement in Psoriasis Area and Severity Index) to year 5 in patients with moderate-to-severe plaque psoriasis when used at the dose of 300 mg every 4 weeks. What does this study add? Standard every 4 week (q4w) dosing of secukinumab 300 mg is the optimal regimen to achieve and maintain clear or almost clear skin at week 52; the majority of the patients (85·7%) maintain PASI 90 at week 52. Superiority of intensified (q2w) dosing over the q4w regimen could not be claimed. However, patients with a higher body weight (≥ 90 kg) not achieving PASI 90 response at week 24 may benefit from q2w dosing.
Keyphrases
- body weight
- open label
- ankylosing spondylitis
- placebo controlled
- rheumatoid arthritis
- end stage renal disease
- double blind
- clinical trial
- ejection fraction
- newly diagnosed
- early onset
- chronic kidney disease
- randomized controlled trial
- prognostic factors
- high intensity
- phase ii
- squamous cell carcinoma
- peritoneal dialysis
- study protocol
- soft tissue
- wound healing
- high resolution
- preterm birth
- phase ii study
- single molecule
- combination therapy