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使用注射用生物制剂阿达木单抗、依那西普和乌司奴单抗治疗银屑病患者的特征分析:一项病历回顾研究。

Characterizing patients with psoriasis on injectable biologics adalimumab, etanercept, and ustekinumab: A chart review study.

作者信息

Zhang Mingliang, Goren Amir, Lee Seina, DiBonaventura Marco D, Olson William H

机构信息

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

b Kantar Health , New York , NY , USA , and.

出版信息

J Dermatolog Treat. 2016 Aug;27(4):339-45. doi: 10.3109/09546634.2015.1118427. Epub 2015 Dec 17.

Abstract

OBJECTIVE

This study examined plaque psoriasis (PsO) patient characteristics across injectable biologics.

METHODS

Data were collected from 400 US dermatologists randomly selecting five charts each for patients with PsO (patient n  =  2000): adalimumab (ADA; n  =  447), etanercept (ETA; 539), ustekinumab (UST) 45 mg (511) and UST 90 mg (503). Physicians had to have been in practice 2-30 years, managing 10+  patients (5 + with biologics for PsO). Generalized estimating equation models, weighted according to inverse probability of patient selection and accounting for patient correlation within physicians, examined patient measures as a function of treatment (UST 90 mg = reference).

RESULTS

Patients on UST 90 mg had higher odds of weighing  >100 kg (adjusted mean  =  34.4%) vs. ADA (10.9%), ETA (5.5%) or UST 45 mg (6.8%), greater body surface affected and higher odds of severe PsO prior to treatment and higher odds of prior biologics use. Mean prior biologics used was higher with UST 90 mg versus ADA or ETA. Number of comorbidities was higher with UST 90 mg versus ETA or UST 45 mg.

CONCLUSIONS

Among biologics-treated patients with PsO, UST 90 mg appears to be used in patients with greater weight, baseline severity and prior biologics experience than ADA, ETA or UST 45 mg. UST 90 mg is used in patients with more comorbidities than other treatments except ADA.

摘要

目的

本研究调查了使用注射用生物制剂治疗的斑块状银屑病(PsO)患者的特征。

方法

从400名美国皮肤科医生处收集数据,这些医生为PsO患者(患者总数n = 2000)每人随机选取5份病历:阿达木单抗(ADA;n = 447)、依那西普(ETA;539)、45 mg优特克单抗(UST)(511)和90 mg UST(503)。医生必须从业2至30年,管理10名以上患者(其中5名以上使用生物制剂治疗PsO)。采用广义估计方程模型,根据患者选择的逆概率进行加权,并考虑医生内部患者的相关性,将患者指标作为治疗的函数进行检验(90 mg UST = 参照组)。

结果

与ADA(10.9%)、ETA(5.5%)或45 mg UST(6.8%)相比,使用90 mg UST的患者体重>100 kg的几率更高(校正均值 = 34.4%),治疗前受影响的体表面积更大,重度PsO的几率更高,且先前使用生物制剂的几率更高。与ADA或ETA相比,90 mg UST患者先前使用生物制剂的平均次数更多。与ETA或45 mg UST相比,90 mg UST患者的合并症数量更多。

结论

在接受生物制剂治疗的PsO患者中,与ADA、ETA或45 mg UST相比,90 mg UST似乎用于体重更大、基线病情更严重且有生物制剂使用经验的患者。与除ADA之外的其他治疗相比,90 mg UST用于合并症更多的患者。

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