Persistence and Dose Escalation During Maintenance Phase and Use of Nonbiologic Medications Among Patients With Ulcerative Colitis Initiated on Ustekinumab in the United States.

IF 1.8 Q3 GASTROENTEROLOGY & HEPATOLOGY Crohn's & Colitis 360 Pub Date : 2023-07-01 DOI:10.1093/crocol/otad045
Maryia Zhdanava, Ruizhi Zhao, Ameur M Manceur, Sumesh Kachroo, Patrick Lefebvre, Dominic Pilon
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Abstract

Background: Real-world data on treatment patterns among patients with ulcerative colitis (UC) initiated on ustekinumab are limited.

Methods: Adults with UC initiated on ustekinumab (index date) between 10/18/2019 and 04/31/2022 were selected from a deidentified health insurance claims database (Symphony Health, an ICON plc Company, PatientSource). Persistence (no gaps in days of supply >120 days), persistence while being corticosteroid-free (no corticosteroid use for ≥14 days of supply after a 90-day grace period from index date) and dose escalation (≥2 consecutive subcutaneous claims ≥100% above daily maintenance dose) were described during the maintenance phase using Kaplan-Meier analysis. Nonbiologic treatments, among patients with ≥2 ustekinumab claims within 90 days post-index and ≥6 months of follow-up, were compared with logistic models 6 months post- versus pre-ustekinumab initiation.

Results: 6565 patients on ustekinumab entered the maintenance phase. At month 12 of the maintenance phase, 72.0% (95% confidence interval [CI]: 70.1%-73.9%) were persistent, 50.8% (95% CI: 48.7%-52.9%) were persistent and corticosteroid-free, and 19.2% (95% CI: 17.3%-21.3%) of patients had dose escalation. In the 6 months post- versus pre-ustekinumab initiation, the odds of nonbiologic medication use assessed in 4147 patients were significantly lower: 57% lower odds for corticosteroid, 46% for 60 cumulative days of corticosteroid, 42% for 5-aminosalicylic acid, and 24% for immunomodulators (all P < .001).

Conclusions: Most patients with UC reaching the maintenance phase on ustekinumab remained persistent after 12 months of maintenance therapy. Nonbiologic medication use post-ustekinumab initiation was significantly lower, notably for corticosteroids. Given the multiple complications associated with chronic corticosteroid use, this reduction can be seen as clinically relevant and informs treatment choice for patients with UC.

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在美国,Ustekinumab启动的溃疡性结肠炎患者在维持期的持续性和剂量递增以及非生物药物的使用
背景:在ustekinumab启动的溃疡性结肠炎(UC)患者的治疗模式的真实数据是有限的。方法:从确定的健康保险索赔数据库(Symphony health, an ICON plc Company, PatientSource)中选择2019年10月18日至2022年4月31日期间接受ustekinumab治疗的UC成人(索引日期)。使用Kaplan-Meier分析,在维持阶段描述了持续(≥120天的供应天数无间断)、无皮质类固醇的持续(从指数日起90天宽限期后不使用皮质类固醇≥14天)和剂量递增(≥2个连续皮下声明≥100%高于每日维持剂量)。非生物治疗,在指数后90天内≥2个ustekinumab索赔和随访≥6个月的患者中,与ustekinumab开始后6个月与前6个月的logistic模型进行比较。结果:6565例使用ustekinumab的患者进入维持期。在维持期的第12个月,72.0%(95%可信区间[CI]: 70.1%-73.9%)的患者持续使用,50.8% (95% CI: 48.7%-52.9%)的患者持续使用且不使用皮质类固醇,19.2% (95% CI: 17.3%-21.3%)的患者剂量增加。在乌斯特金单抗开始治疗后的6个月内,4147名患者的非生物药物使用几率明显降低:皮质类固醇的几率降低57%,皮质类固醇累计60天的几率降低46%,5-氨基水杨酸的几率降低42%,免疫调节剂的几率降低24%(所有P结论:大多数UC患者在乌斯特金单抗达到维持阶段后,在12个月的维持治疗后仍持续存在。ustekinumab启动后非生物药物的使用显著降低,尤其是皮质类固醇。考虑到与慢性皮质类固醇使用相关的多种并发症,这种减少可以被视为具有临床相关性,并为UC患者的治疗选择提供指导。
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来源期刊
Crohn's & Colitis 360
Crohn's & Colitis 360 Medicine-Gastroenterology
CiteScore
2.50
自引率
0.00%
发文量
41
审稿时长
12 weeks
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