Ding Zhijie, Obando Camilo, Muser Erik, Kozma Chris, Slaton Terra
Janssen Scientific Affairs, LLC, Horsham, PA, USA.
Independent Consultant, St Helena Island, SC, USA.
Drugs Real World Outcomes. 2021 Dec;8(4):565-575. doi: 10.1007/s40801-021-00264-5. Epub 2021 Jun 16.
Real-world evidence for how US Crohn's disease (CD) patients use ustekinumab is limited.
The aim of this study was to describe the persistence, maintenance dosing, and pre-post corticosteroid and opioid use for CD patients in the USA treated with ustekinumab and those treated with adalimumab as a commonly used descriptive reference product.
CD patients aged ≥ 18 years with ≥2 CD diagnoses between 1 October 2012 and 31 May 2018 and ≥ 1 new (i.e., no claim for at least 1 year) outpatient pharmacy claim for ustekinumab or adalimumab (first claim date = index date) on or after 26 September 2016 were selected from Symphony Health database. McNemar's tests were used to derive the p-values for pre-post changes in corticosteroid and opioid use within each treatment cohort.
A total of 1073 ustekinumab and 2904 adalimumab patients met analysis criteria. Using a 90-day rule for discontinuation, persistence at 1 year post-index was 69.8% for ustekinumab and 65.1% for adalimumab. The majority received doses within ±30% of the approved labeling (ustekinumab 81.1%; adalimumab 78.8%). Doses higher than US package insert (PI) recommended maintenance dose were 7.0% for ustekinumab and 13.6% for adalimumab for 30% above PI, respectively; and 4.0% versus 9.4% for 50% above PI, respectively. Rates of pre-index biologic use suggest that patients treated with ustekinumab may have greater CD severity based on a greater percentage being biologic-experienced (ustekinumab 51.5% and adalimumab 8.4%). From pre- to post-index, the relative proportion of ustekinumab patients with ≥ 1 pharmacy claim for corticosteroids decreased by 25.5% (p < 0.0001) and opioids decreased by 8.4% (p = 0.0030). Results for adalimumab (a commonly used descriptive reference product in CD) showed generally similar trends.
In this real-world study, persistence for ustekinumab remained high at 1 year. The majority of the patients in the ustekinumab cohort followed US PI recommended dosing. The percentage of patients with average dose above PI recommendations over 1 year were low for ustekinumab. Reductions in the proportion of patients with claims for corticosteroids or opioids were observed in patients using ustekinumab.
关于美国克罗恩病(CD)患者使用优特克单抗的真实世界证据有限。
本研究旨在描述美国接受优特克单抗治疗的CD患者以及接受阿达木单抗治疗(作为常用的描述性对照产品)的CD患者的持续用药情况、维持剂量,以及皮质类固醇和阿片类药物使用的前后变化。
从Symphony Health数据库中选取2012年10月1日至2018年5月31日期间年龄≥18岁、有≥2次CD诊断且在2016年9月26日或之后有≥1次新的(即至少1年无相关报销记录)门诊药房优特克单抗或阿达木单抗报销记录(首次报销日期=索引日期)的CD患者。使用McNemar检验得出每个治疗队列中皮质类固醇和阿片类药物使用前后变化的p值。
共有1073例优特克单抗患者和2904例阿达木单抗患者符合分析标准。采用90天停药规则,索引日期后1年的持续用药率,优特克单抗为69.8%,阿达木单抗为65.1%。大多数患者接受的剂量在批准标签规定剂量的±30%范围内(优特克单抗为81.1%;阿达木单抗为78.8%)。高于美国药品说明书(PI)推荐维持剂量30%的剂量,优特克单抗为7.0%,阿达木单抗为13.6%;高于PI推荐剂量50%的剂量,优特克单抗为4.0%,阿达木单抗为9.4%。索引日期前生物制剂的使用比例表明,接受优特克单抗治疗的患者可能病情更严重,因为有更大比例的患者有生物制剂使用经验(优特克单抗为51.5%,阿达木单抗为8.4%)。从索引日期前到索引日期后,有≥1次皮质类固醇药房报销记录的优特克单抗患者相对比例下降了25.5%(p<0.0001),有阿片类药物报销记录的患者相对比例下降了8.4%(p=0.0030)。阿达木单抗(CD中常用的描述性对照产品)的结果显示出大致相似的趋势。
在这项真实世界研究中,优特克单抗在1年时的持续用药率仍然很高。优特克单抗队列中的大多数患者遵循美国PI推荐的剂量。优特克单抗患者中超过1年平均剂量高于PI推荐剂量的比例较低。使用优特克单抗的患者中,有皮质类固醇或阿片类药物报销记录的患者比例有所下降。