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美国成人炎症性肠病中生物制剂的依从性、持久性、转换和剂量升级的真实世界证据:系统评价。

Real-world evidence on adherence, persistence, switching and dose escalation with biologics in adult inflammatory bowel disease in the United States: A systematic review.

机构信息

RTI Health Solutions, Research Triangle Park, North Carolina.

Janssen Scientific Affairs, LLC, Horsham, Pennsylvania.

出版信息

J Clin Pharm Ther. 2019 Aug;44(4):495-507. doi: 10.1111/jcpt.12830. Epub 2019 Mar 14.

Abstract

WHAT IS KNOWN AND OBJECTIVE

The application of biologics to treat inflammatory bowel disease (IBD), including Crohn's disease and ulcerative colitis, is well established. Our aim was to characterize the most recent five years of data on rates of adherence, persistence, switching and dose escalations with biologics used to treat IBD in the United States.

METHODS

We systematically reviewed electronic databases MEDLINE, MEDLINE In-Process, EMBASE and Cochrane Library for 2012-2017 as well as conference proceedings for 2016-2017 published in English.

RESULTS AND DISCUSSION

Of 449 records identified, 41 met all screening criteria. Published studies varied greatly in methodology, data sources, population studied, follow-up time and endpoint definitions, preventing meaningful comparisons across studies. Based on studies using a medication possession rate threshold of <80% or <86%, 38%-77% of patients were found non-adherent to biologics. Discontinuation within the first 3 months occurred in 0%-25% of patients in six studies; 7%-65% discontinued by 12 months in 13 studies. Among all patients who initiated an index biologic, the switch rate to another biologic ranged from 4.5% to 20% in 6 studies. Dose escalations were reported in only four studies; 8%-35% of patients had their dose escalated within the first year of therapy.

WHAT IS NEW AND CONCLUSION

This study demonstrates variability in study design and methodology to assess adherence, persistence, switching and dose escalation with biologics among adults with IBD in the United States. Our findings suggest that real-world biologic use may be suboptimal and indicate new therapies and/or additional patient support may be needed.

摘要

已知和目的

生物制剂在治疗炎症性肠病(IBD),包括克罗恩病和溃疡性结肠炎中的应用已经得到充分证实。我们的目的是描述美国最近五年关于生物制剂治疗 IBD 的依从性、持续性、转换和剂量升级的数据特征。

方法

我们系统地检索了 MEDLINE、MEDLINE In-Process、EMBASE 和 Cochrane 图书馆 2012-2017 年的电子数据库以及 2016-2017 年以英文发表的会议记录。

结果与讨论

在 449 条记录中,有 41 条符合所有筛选标准。已发表的研究在方法学、数据来源、研究人群、随访时间和终点定义方面差异很大,使得难以在研究之间进行有意义的比较。基于使用药物占有比率阈值<80%或<86%的研究,38%-77%的患者被发现对生物制剂不依从。在 6 项研究中,有 0%-25%的患者在治疗的前 3 个月内停药;在 13 项研究中,有 7%-65%的患者在 12 个月内停药。在所有开始使用索引生物制剂的患者中,有 6 项研究报告的转换率为另一种生物制剂的比例为 4.5%-20%。只有 4 项研究报告了剂量升级;在治疗的第一年,有 8%-35%的患者增加了剂量。

新内容和结论

本研究表明,在美国成年人 IBD 中,评估生物制剂的依从性、持续性、转换和剂量升级的研究设计和方法存在差异。我们的研究结果表明,实际应用生物制剂可能并不理想,表明可能需要新的治疗方法和/或额外的患者支持。

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