Effect of Leflunomide on Pegloticase Response Rate in Patients with Uncontrolled Gout: A Retrospective Study

被引:6
|
作者
Masri, Karim Richard [1 ]
Padnick-Silver, Lissa [2 ]
Winterling, Kevin [2 ]
LaMoreaux, Brian [2 ,3 ]
机构
[1] Bon Secours Rheumatol Ctr, Richmond, VA USA
[2] Horizon Therapeut, Lake Forest, IL USA
[3] 1 Horizon Way, Deerfield, IL 60061 USA
关键词
Uncontrolled gout; Refractory gout; Pegloticase; Leflunomide; Immunomodulation; MODIFYING ANTIRHEUMATIC DRUGS; ACTIVE RHEUMATOID-ARTHRITIS; EFFICACY; TOLERABILITY; PLACEBO;
D O I
10.1007/s40744-021-00421-w
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Pegloticase, a PEGylated uricase for uncontrolled gout, rapidly lowers serum urate (SU). Not all patients complete a full-therapy course because anti-pegloticase antibodies can develop, causing efficacy loss and infusion reactions. The literature and clinical trial data indicate that methotrexate co-administration markedly improves pegloticase response rates from the established monotherapy response rate of 42%. Unfortunately, methotrexate use is restricted by kidney disease, which is often present in uncontrolled gout patients. Leflunomide is less restricted in patients with renal dysfunction. This study examined the treatment response rate of pegloticase co-administered with leflunomide. Methods Patients co-treated with pegloticase (8 mg biweekly infusion) and oral leflunomide (20 mg/day) were included. Patient/treatment characteristics and safety parameters (adverse events [AEs], laboratory parameters) were examined. Pre-infusion prophylaxis was administered (day of infusion: IV solumedrol, night before and morning of infusion: oral fexofenadine or diphenhydramine). Patients were considered treatment responders if >= 12 pegloticase infusions were administered and pre-infusion SU < 6 mg/dl at infusion-12. Results Ten patients (five male, 72.7 +/- 12.5 years) were included. The most common comorbidities were chronic kidney disease (90%), hypertension (70%), diabetes mellitus (60%), obesity (60%), and congestive heart failure (50%). Baseline SU was 7.1 +/- 2.4 mg/dl and nine patients (90%) had subcutaneous tophi noted. Seven patients (70%) met responder criteria, receiving 26.6 +/- 14.0 infusions (range 13-55) with a pre-infusion-12 SU of 0.9 +/- 1.5 mg/dl. The three non-responders received < 12 infusions because of unrelated AEs or loss of follow-up. Three patients (30%) experienced AEs. One had unrelated cardiac disease worsening and three gout flares, one had a pre-infusion solumedrol reaction (wooziness/loss of consciousness), and one had two mild, transient increases in liver enzymes. Conclusions This study supports leflunomide as co-therapy to pegloticase in uncontrolled gout patients. Heterogeneity and high comorbidity burden in uncontrolled gout patients makes having a variety of immunomodulators options important.
引用
收藏
页码:555 / 563
页数:9
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