Table 1.
Comparison of IL‐1 Antagonists Used in Recurrent Pericarditis in Adults
Anakinra | Rilonacept | Canakinumab | |
---|---|---|---|
Ultrastructure | Recombinant protein | Fc fusion protein | IgG monoclonal antibody |
IL‐1 α receptor antagonist | + | + | − |
IL‐1 β receptor antagonist | + | + | + (Binds plasma IL‐ β and prevents interaction with receptor) |
Half‐life | 4 to 6 h | 7 d | 22 to 26 d |
Frequency of administration | Daily | Weekly | Every 4 to 8 wks |
Administration route | Subcutaneous intravenous | Subcutaneous | Subcutaneous |
Loading dose | − | 320 mg | − |
Maintenance dose | 2 mg/kg (up to 100 mg) | 160 mg | 4 mg/kg or 150 mg (single dose) |
Duration of treatment | 6 to 12 months (can extend in patients with recurrences) | 9 months with range of 3 to 14 months (can extend in patients with recurrence) | Up to 2 y |
Dose adjustment for renal impairment |
CrCl ≥30 mL/min: not required CrCl <30 mL/min or ESRD: consider changing dose to every other day. Not dialyzable (<2.5%) |
Not required |
Not required |
Dose adjustment for hepatic impairment | Not required | Not required | Not required |
Adverse events | Injection site reactions, hepatitis, infections | Injection site reactions, infections, neutropenia, hyperlipemia | Injection site reactions, infections, neutropenia |
Monitoring | CBC, CRP, symptoms/signs of infection, hepatitis B and TB screening at baseline | CBC, CRP, lipid profile, symptoms/signs of infection, hepatitis B and TB screening at baseline | CBC, CRP, symptoms/signs of infections, hepatitis B and TB screening at baseline |
Main clinical evidence in pericarditis |
|
RHAPSODY Phase III clinical trial and Phase II study. | Case reports & Case Serie |
CBC indicates complete blood count; CrCl, creatinine clearance; CRP, C‐reactive protein; Fc, fragment crystallizable region; IL, interleukin; and TB, tuberculosis.