Suppr超能文献

银屑病合并胃肠道疾病患者中阿普米司特的早期停药:发生率及相关危险因素

Early Discontinuation of Apremilast in Patients with Psoriasis and Gastrointestinal Comorbidities: Rates and Associated Risk Factors.

作者信息

Schmidt Lana, Wang Ching An, Patel Vardhaman, Davidson David, Kalirai Samaneh, Panda Ankita, Seigel Lauren

机构信息

Springfield Clinic, Effingham, IL, USA.

Bristol Myers Squibb, Princeton, NJ, USA.

出版信息

Dermatol Ther (Heidelb). 2023 Sep;13(9):2019-2030. doi: 10.1007/s13555-023-00975-3. Epub 2023 Jul 30.

Abstract

INTRODUCTION

Apremilast, the first oral targeted treatment for moderate to severe psoriasis, is associated with diarrhea, nausea, and vomiting, which have contributed to treatment discontinuation. This study describes early apremilast discontinuation rates in patients with psoriasis, including a cohort with gastrointestinal (GI) comorbidities, and associated characteristics.

METHODS

This retrospective cohort study used IBM (now Merative™) MarketScan commercial and Medicare claims data to identify adults with psoriasis who filled their first apremilast prescription between September 1, 2014 and March 31, 2020. Discontinuation was defined as a gap of > 30 days after exhausting the days' supply of a prescription fill. The GI comorbidity cohort included patients with ≥ 1 claim for inflammatory bowel disease (IBD), irritable bowel syndrome (IBS), or other GI comorbidity during the study period.

RESULTS

Discontinuation rates were high, regardless of previous biologic treatment or GI comorbidities. Among all patients, 25.5% discontinued within 60 days and 56.4% discontinued within 180 days. Patients who discontinued were more likely to be younger, female, and have IBD, Crohn's disease, or a mental health disorder. At 180 days, patients who used biologics previously were more likely to discontinue than biologic-naive patients. Patients with IBD discontinued at a greater rate than those without IBD at 60 days (30.3% vs 24.4%; P = 0.018) and 180 days (63.6% vs 57.2%; P = 0.026). Differences in discontinuation rates were minimal between GI comorbidity groups; patients with IBS discontinued at numerically higher rates than those without IBS.

CONCLUSIONS

High rates of early discontinuation were observed for patients with and without GI comorbidities. Early discontinuation, whether attributable to poor tolerability or effectiveness, suggests the need for additional oral treatment options.

摘要

简介

阿普米拉斯是首个用于治疗中度至重度银屑病的口服靶向药物,与腹泻、恶心和呕吐有关,这些不良反应导致了治疗中断。本研究描述了银屑病患者早期停用阿普米拉斯的比率,包括患有胃肠道(GI)合并症的队列以及相关特征。

方法

这项回顾性队列研究使用IBM(现为Merative™)市场扫描商业和医疗保险理赔数据,以识别在2014年9月1日至2020年3月31日期间首次开具阿普米拉斯处方的成年银屑病患者。停药定义为在处方药物供应天数用尽后间隔超过30天。胃肠道合并症队列包括在研究期间有≥1次炎症性肠病(IBD)、肠易激综合征(IBS)或其他胃肠道合并症索赔记录的患者。

结果

无论先前是否接受过生物治疗或有无胃肠道合并症,停药率都很高。在所有患者中,25.5%在60天内停药,56.4%在180天内停药。停药的患者更可能是年轻女性,并且患有IBD、克罗恩病或精神疾病。在180天时,先前使用过生物制剂的患者比未使用过生物制剂的患者更有可能停药。IBD患者在60天(30.3%对24.4%;P = 0.018)和180天(63.6%对57.2%;P = 0.026)时的停药率高于无IBD患者。胃肠道合并症组之间的停药率差异最小;IBS患者的停药率在数值上高于无IBS患者。

结论

有或无胃肠道合并症的患者早期停药率均较高。早期停药,无论归因于耐受性差还是疗效不佳,都表明需要更多的口服治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff1b/10442291/282166c5f2f7/13555_2023_975_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验