Masri Karim Richard, Padnick-Silver Lissa, Winterling Kevin, LaMoreaux Brian
Bon Secours Rheumatology Center, Richmond, VA, USA.
Horizon Therapeutics, Lake Forest, IL, USA.
Rheumatol Ther. 2022 Apr;9(2):555-563. doi: 10.1007/s40744-021-00421-w. Epub 2022 Jan 8.
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.
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.
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.
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.
聚乙二醇化尿酸酶培戈洛酶用于治疗难治性痛风,可迅速降低血清尿酸盐(SU)水平。并非所有患者都能完成整个疗程,因为可能会产生抗培戈洛酶抗体,导致疗效丧失和输液反应。文献和临床试验数据表明,联合使用甲氨蝶呤可使培戈洛酶的反应率从既定的单药治疗反应率42%显著提高。不幸的是,甲氨蝶呤的使用受肾脏疾病限制,而难治性痛风患者常伴有肾脏疾病。来氟米特在肾功能不全患者中的使用限制较少。本研究探讨了培戈洛酶与来氟米特联合使用的治疗反应率。
纳入接受培戈洛酶(每两周静脉输注8mg)和口服来氟米特(每日20mg)联合治疗的患者。检查患者/治疗特征和安全参数(不良事件[AEs]、实验室参数)。进行输液前预防(输液当天:静脉注射甲泼尼龙;输液前一晚和当天上午:口服非索非那定或苯海拉明)。如果给予≥12次培戈洛酶输注且输液前12次时SU<6mg/dl,则患者被视为治疗反应者。
纳入10例患者(5例男性,年龄72.7±12.5岁)。最常见的合并症为慢性肾脏病(90%)、高血压(70%)、糖尿病(60%)、肥胖(60%)和充血性心力衰竭(50%)。基线SU为7.1±2.4mg/dl,9例患者(90%)有皮下痛风石。7例患者(70%)符合反应者标准,接受了26.6±14.0次输注(范围13 - 55次),输液前12次时SU为0.9±1.5mg/dl。3例无反应者因无关的不良事件或失访而接受的输注次数<12次。3例患者(30%)发生了不良事件。1例患者出现无关的心脏病加重和3次痛风发作,1例患者发生输液前甲泼尼龙反应(头晕/意识丧失),1例患者出现两次轻度、短暂的肝酶升高。
本研究支持来氟米特作为难治性痛风患者培戈洛酶的联合治疗药物。难治性痛风患者的异质性和高合并症负担使得拥有多种免疫调节剂选择很重要。