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美国接受乌司奴单抗处方治疗的克罗恩病患者的真实世界持续用药情况、维持剂量以及皮质类固醇和阿片类药物使用前后情况

Real-World Persistence, Maintenance Dosing, and Pre-Post Corticosteroid and Opioid Use Among Crohn's Disease Patients with Prescription Claims for Ustekinumab in the USA.

作者信息

Ding Zhijie, Obando Camilo, Muser Erik, Kozma Chris, Slaton Terra

机构信息

Janssen Scientific Affairs, LLC, Horsham, PA, USA.

Independent Consultant, St Helena Island, SC, USA.

出版信息

Drugs Real World Outcomes. 2021 Dec;8(4):565-575. doi: 10.1007/s40801-021-00264-5. Epub 2021 Jun 16.

Abstract

BACKGROUND

Real-world evidence for how US Crohn's disease (CD) patients use ustekinumab is limited.

OBJECTIVES

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.

METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

背景

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。

目的

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。

方法

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。

结果

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。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9ab/8605940/e42c9bfcf5b1/40801_2021_264_Fig1_HTML.jpg

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