Urate-lowering therapy, serum urate, inflammatory biomarkers, and renal function in patients with gout following pegloticase discontinuation

被引:1
作者
Holladay, Emily E. [1 ]
Mudano, Amy S. [2 ]
Xie, Fenglong [1 ]
Zhang, Jingyi [1 ]
Mikuls, Ted R. [3 ,4 ]
Lamoreaux, Brian [5 ]
Padnick-Silver, Lissa [5 ]
Curtis, Jeffrey R. [1 ,2 ]
机构
[1] Univ Alabama Birmingham, 1825 Univ Blvd, Birmingham, AL 35233 USA
[2] Fdn Advancing Sci Technol Educ & Res, Birmingham, AL 35244 USA
[3] Univ Nebraska, Med Ctr, Omaha, NE USA
[4] VA Nebraska Western Iowa Hlth Care Syst, Omaha, NE USA
[5] Amgen Inc, Horizon Therapeut Plc, Deerfield, IL USA
关键词
Gout; Pegloticase; Treatment gap; Restart; Discontinuation; CHRONIC KIDNEY-DISEASE; EFFICACY; TOLERABILITY; MANAGEMENT; ARTHRITIS;
D O I
10.1186/s13075-024-03318-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background/Purpose Little is known about long-term clinical outcomes or urate-lowering (ULT) therapy use following pegloticase discontinuation. We examined ULT use, serum urate (SU), inflammatory biomarkers, and renal function following pegloticase discontinuation. Methods We conducted a retrospective analysis of gout patients who discontinued pegloticase using the Rheumatology Informatics System for Effectiveness (RISE) registry from 1/2016 to 6/2022. We defined discontinuation as a gap >= 12 weeks after last infusion. We examined outcomes beginning two weeks after last dose and identified ULT therapy following pegloticase discontinuation. We evaluated changes in lab values (SU, eGFR, CRP and ESR), comparing on- treatment (<= 15 days of the second pegloticase dose) to post-treatment. Results Of the 375 gout patients discontinuing pegloticase, median (IQR) laboratory changes following discontinuation were: SU: +2.4 mg/dL (0.0,6.3); eGFR: -1.9 mL/min (- 8.7,3.7); CRP: -0.8 mg/L (-12.8,0.0); and ESR: -4.0 mm/hr (-13.0,0.0). Therapy post-discontinuation included oral ULTs (86.0%), restarting pegloticase (4.5%), and no documentation of ULT (9.5%), excluding patients with multiple same-day prescriptions (n = 17). Oral ULTs following pegloticase were: 62.7% allopurinol, 34.1% febuxostat. The median (IQR) time to starting/restarting ULT was 92.0 days (55.0,173.0). Following ULT prescribing (>= 30 days), only 51.0% of patients had SU < 6 mg/dL. Patients restarting pegloticase achieved a median SU of 0.9 mg/dL (IQR:0.2,9.7) and 58.3% had an SU < 6 mg/dL. Conclusion Pegloticase treats uncontrolled gout in patients with failed response to xanthine oxidase inhibitors, but among patients who discontinue, optimal treatment is unclear. Based on this analysis, only half of those starting another ULT achieved target SU. Close follow-up is needed to optimize outcomes after pegloticase discontinuation.
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页数:11
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