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抗TNF生物类似药转换的最新进展——真实世界的临床有效性和安全性

An Update on Anti-TNF Biosimilar Switching-Real-World Clinical Effectiveness and Safety.

作者信息

Meade Susanna, Squirell Elizabeth, Hoang Thomas Tam, Chow James, Rosenfeld Gregory

机构信息

University of British Columbia, Vancouver, BC V6T 1Z4, Canada.

BioPro Biologics Pharmacy, 845 West Broadway, Vancouver, BC V5Z1J9, Canada.

出版信息

J Can Assoc Gastroenterol. 2023 Oct 25;7(1):30-45. doi: 10.1093/jcag/gwad027. eCollection 2024 Feb.

Abstract

BACKGROUND

Biological medications for inflammatory bowel disease (IBD) account for a significant burden on provincial budgets. In an effort to curb these rising costs, nationwide switching to biosimilars is expected to be complete in Canada before the end of 2023. Biosimilar products do not require the same rigor for licensing as the originator and therefore there has been appropriate scepticism as to how biosimilars will perform in real-world practice.

METHODS

We have performed a systematic review including real-world observational studies of adult patients with IBD. The primary outcome was clinical effectiveness and/or safety in patients who had switched from originator to biosimilar anti-TNF. Secondary outcomes included loss of response (LOR), treatment persistence or cessation and immunogenicity.

RESULTS

We included 43 studies (7,462 patients [70 percent Crohn's disease: 30 percent ulcerative colitis]; 32 infliximab studies, and 11 adalimumab studies). For infliximab, 75 percent patients were in clinical remission at the time of switch and 75 percent maintained clinical remission beyond 12 months, compared to 78 percent of patients who continued originator. For adalimumab, 86 percent patients were in remission at the time of switch with 82 percent maintaining remission at 6 months follow-up. Injection site pain was higher in patients who switched to a citrate containing adalimumab biosimilar, compared with those who continued originator. All other outcomes (LOR, treatment cessation or persistence and serious adverse events) were similar to patients who continued originator (in comparator cohorts or the available literature).

CONCLUSION

Whilst ongoing vigilance is required, these data are reassuring to both patients and clinicians and will significantly help to reduce health-care costs across Canada.

摘要

背景

炎症性肠病(IBD)的生物药物给省级预算带来了沉重负担。为了遏制这些不断上升的成本,加拿大预计在2023年底前在全国范围内完成向生物类似药的转换。生物类似药产品在许可方面不需要与原研药相同的严格程度,因此人们对生物类似药在实际临床中的表现存在合理的怀疑。

方法

我们进行了一项系统评价,纳入了对成年IBD患者的真实世界观察性研究。主要结局是从原研抗TNF药物转换为生物类似药的患者的临床有效性和/或安全性。次要结局包括反应丧失(LOR)、治疗持续性或停药情况以及免疫原性。

结果

我们纳入了43项研究(7462例患者[70%为克罗恩病:30%为溃疡性结肠炎];32项英夫利昔单抗研究和11项阿达木单抗研究)。对于英夫利昔单抗,转换时75%的患者处于临床缓解状态,超过12个月后75%的患者维持临床缓解,而继续使用原研药的患者这一比例为78%。对于阿达木单抗,转换时86%的患者处于缓解状态,随访6个月时82%的患者维持缓解。与继续使用原研药的患者相比,转换为含柠檬酸盐的阿达木单抗生物类似药的患者注射部位疼痛发生率更高。所有其他结局(LOR、治疗停药或持续性以及严重不良事件)与继续使用原研药的患者(在对照队列或现有文献中)相似。

结论

虽然仍需持续警惕,但这些数据让患者和临床医生都感到安心,并将显著有助于降低加拿大的医疗保健成本。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acc9/10836972/787cb8db8c13/gwad027_fig1.jpg

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