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阿普司特在银屑病关节炎患者中的治疗持续性

Treatment Persistence of Apremilast Among Patients with Psoriatic Arthritis.

作者信息

Haddad Amir, Stein Nili, Lavi Idit, Shynkar Lisa, Bergman Irina, Feldhamer Ilan, Cohen Arnon Dov, Saliba Walid, Zisman Devy

机构信息

Rheumatology Unit, Carmel Medical Center, Haifa, Israel.

Department of Epidemiology, Clalit Health Services, Haifa, Israel.

出版信息

Biologics. 2023 Oct 4;17:129-136. doi: 10.2147/BTT.S425693. eCollection 2023.

Abstract

INTRODUCTION

Persistence in drug therapy reflects treatment effectiveness and tolerability. We aim to estimate the persistence of apremilast prescribed to patients with psoriatic arthritis (PsA) and to identify characteristics associated with treatment discontinuation in a real-world setting.

METHODS

Patients with PsA treated with apremilast from January 2016 were identified from a large health database and followed until medication stop date (using 3-months grace period), death or the end of observation period (June 2021). Demographic data, Charlson comorbidity index and concomitant and previous use of conventional and biologic DMARDs were extracted. The reasons for drug discontinuation were manually retrieved from patient charts. Time to discontinuation was estimated using survival analysis using Kaplan-Meier functions.

RESULTS

Overall, 568 PsA patients treated with apremilast were identified. The mean age was 55.3±14.0 years, of whom 332 (58.5%) were females, 38.4% were obese (BMI>30), 75.2% had a Charlson comorbidity index>1, 24.1% were on concomitant treatment with methotrexate and 72.4% were biologic naïve. The median persistent period was 6.1,95% CI (5.2-6.9) months in which only 16.9% remained persistent on apremilast. No difference was found with regard to age, sex, socioeconomic status, ethnicity and obesity between patients who were persistent compared to patients who discontinued apremilast. Concomitant treatment with methotrexate and prior history of biologic therapy did not affect drug persistency (log rank P=0.957 and 0.082, respectively). Causes for treatment discontinuation were due to lack of skin efficacy in 19.4%, lack of joint efficacy in 33.3%, combined skin and joint inefficacy at 2.3% and due to side effects in 24.1%.

CONCLUSION

In this large observational retrospective cohort of patients treated with apremilast, a relatively low drug persistence was observed with 6-month and 1-year survival rates of 50.3% and 31.3%, respectively. Treatment discontinuation was mainly due to joint inefficacy, advocating for more studies for proper patient selection to assure treatment effectiveness and persistency.

摘要

引言

药物治疗的持续性反映了治疗效果和耐受性。我们旨在评估为银屑病关节炎(PsA)患者开具的阿普米司特的持续性,并确定在实际临床环境中与治疗中断相关的特征。

方法

从一个大型健康数据库中识别出2016年1月开始接受阿普米司特治疗的PsA患者,并随访至停药日期(使用3个月宽限期)、死亡或观察期结束(2021年6月)。提取人口统计学数据、查尔森合并症指数以及传统和生物性抗风湿药物(DMARDs)的合并用药及既往用药情况。从患者病历中人工检索停药原因。使用Kaplan-Meier函数通过生存分析估计停药时间。

结果

总体而言,共识别出568例接受阿普米司特治疗的PsA患者。平均年龄为55.3±14.0岁,其中332例(58.5%)为女性,38.4%为肥胖患者(BMI>30),75.2%的查尔森合并症指数>1,24.1%的患者同时接受甲氨蝶呤治疗,72.4%的患者既往未使用过生物制剂。中位持续时间为6.1个月,95%置信区间(5.2 - 6.9),其中只有16.9%的患者持续使用阿普米司特。在持续使用阿普米司特的患者与停药的患者之间,在年龄、性别、社会经济地位、种族和肥胖方面未发现差异。同时使用甲氨蝶呤和既往生物治疗史均未影响药物持续性(对数秩检验P分别为0.957和0.082)。停药原因包括皮肤疗效不佳占19.4%、关节疗效不佳占33.3%、皮肤和关节联合疗效不佳占2.3%以及副作用占24.1%。

结论

在这个接受阿普米司特治疗的大型观察性回顾性队列中,观察到药物持续性相对较低,6个月和1年生存率分别为50.3%和31.3%。治疗中断主要是由于关节疗效不佳,建议开展更多研究以进行恰当的患者选择,以确保治疗效果和持续性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7e9/10560465/1762b4f222d2/BTT-17-129-g0001.jpg

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