What is the treatment protocol for a patient with moderate to severe plaque psoriasis, including dosing and monitoring for secukinumab (secukinumab), considering their overall health and past medical history?

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Secukinumab Treatment Protocol for Moderate-to-Severe Plaque Psoriasis

Pre-Treatment Screening Requirements

Before initiating secukinumab, screen for active tuberculosis, active infections or sepsis, untreated hepatitis B, and assess for history of inflammatory bowel disease. 1

  • Screen for active tuberculosis and consider anti-tuberculosis therapy before starting secukinumab in patients with latent TB 2
  • Do not initiate during active infection; if active infection or sepsis is present, consult infectious disease specialists before starting therapy 1
  • Untreated hepatitis B infection is a relative contraindication 1
  • Assess for inflammatory bowel disease history, as secukinumab may increase the risk of new-onset or exacerbation of Crohn's disease or ulcerative colitis 2, 1
  • Complete indicated vaccinations before starting therapy 3

Dosing Protocol

Administer secukinumab 300 mg subcutaneously at weeks 0,1,2,3, and 4 (loading phase), followed by 300 mg every 4 weeks starting at week 8 (maintenance phase). 2, 1, 4

  • The 300 mg dose is given as two injections of 150 mg or one injection using the 300 mg/2 mL UnoReady pen 2, 4
  • Self-administration by subcutaneous injection is the standard route 1, 5
  • Avoid injecting into areas of skin showing active psoriasis 2
  • The 300 mg dose is more effective than 150 mg and should be prioritized 1

Special Dosing Considerations for Body Weight

For patients with body weight ≥90 kg who do not achieve adequate response, consider increasing maintenance dosing frequency to 300 mg every 2 weeks. 2, 6

  • Standard every 4-week dosing maintains PASI 90 response in 85.7% of patients at week 52 6
  • Patients weighing ≥90 kg not achieving PASI 90 at week 24 may benefit from every 2-week dosing (57.1% vs 40% PASI 90 response) 6

Response Assessment Timeline

Assess treatment response at week 16; if no response is achieved, consider discontinuation. 2

  • At week 16, expect 79% of patients to achieve PASI 90 with 300 mg secukinumab 1
  • Response is maintained through 52 weeks and beyond with continued dosing 1
  • Consider discontinuation if no response after 16 weeks of treatment 2

Monitoring During Treatment

Monitor for mucocutaneous candida infections, which occur at 1.9 per 100 patient-years but are typically mild and responsive to standard antifungal treatment. 1

  • Most infections are non-serious, mild-to-moderate upper respiratory tract infections (e.g., nasopharyngitis) that do not require treatment discontinuation 2
  • Serious infections occur at low rates (0.015 per patient-year) but require treatment discontinuation until resolved 2, 1
  • Monitor patients with serious infection closely and do not administer secukinumab until the infection resolves 2
  • Neutropenia may occur but is usually mild, transient, and reversible 2
  • Watch for signs of inflammatory bowel disease; if new-onset or exacerbation occurs, discontinue secukinumab 2

Combination Therapy Considerations

Secukinumab is recommended as monotherapy; combination with topical corticosteroids or vitamin D analogues may be considered, though published safety data on combinations is limited. 2, 1

  • Combination with high-potency topical corticosteroids with or without vitamin D analogues can augment efficacy 2
  • No evidence supports combining secukinumab with other biologics, and such combinations carry unknown risks 1

Immunogenicity

  • Less than 1% of patients develop antibodies to secukinumab up to 52 weeks of treatment 2
  • Treatment-emergent anti-drug antibodies occur in less than 0.5% of patients 7

Dosing Interval Adjustments

Maintain standard every 4-week dosing for optimal disease control; extending to every 6-week dosing results in inferior response rates. 6

  • Every 6-week dosing maintained PASI 90 in only 74.9% vs 85.7% with every 4-week dosing at week 52 6
  • Retreatment-as-needed regimens are inferior to fixed-interval maintenance dosing 7

Pharmacokinetic Considerations

  • Steady-state concentrations are achieved by week 24 following every 4-week dosing 4
  • Mean steady-state trough concentrations with 300 mg dosing are 34.4 ± 16.6 mcg/mL 4
  • Bioavailability ranges from 55% to 77% following subcutaneous administration 4
  • Mean elimination half-life is 22 to 31 days 4

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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