Methods and kits for predicting infusion reaction risk and antibody-mediated loss of response by monitoring serum uric acid during pegylated uricase therapy
Methods and kits for predicting infusion reaction risk and antibody-mediated loss of response during intravenous PEGylated uricase therapy in gout patients is provided. Routine SUA monitoring can be used to identify patients receiving PEGylated uricase who may no longer benefit from treatment and who are at greater risk for infusion reactions.
1. A method for reducing likelihood of infusion reactions during PEGylated uricase therapy in a gout patient without measuring anti-PEGylated uricase and anti-PEG antibody titers, comprising the steps of:
intravenously administering to said patient a therapeutically effective amount of PEGylated uricase every two weeks;
obtaining a biological sample from said patient after a period of at least 2 weeks, wherein said biological sample is selected from the group consisting of blood, serum and plasma;
measuring a uric acid level in said biological sample; and
indicating that the uric acid level is associated with a lower likelihood of antibody-mediated PEGylated uricase clearance when said uric acid level is maintained at less than 6 mg/dl or indicating that said uric acid level is associated with a higher likelihood of antibody-mediated PEGylated uricase clearance at a time point when said uric acid level is measured at least 6 mg/dl;
if said uric acid level is less than 6 mg/dl then continuing said administration of PEGylated uricase every two weeks; or
if said uric acid level is above 6 mg/dl then discontinuing said administration of PEGylated uricase every two weeks;
wherein said patient previously received ineffective allopurinol therapy or has a medical history in which allopurinol therapy is contraindicated.
2. The method according to claim 1 , wherein said gout is refractory.
3. The method according to claim 1 , wherein said gout is chronic or tophaceous.