Is the use of secukinumab after anti-TNF therapy greater than expected for the risk of developing inflammatory bowel disease?

Fatih Albayrak , Mustafa Gür , Ahmet Karataş , Süleyman Serdar Koca , Bünyamin Kısacık
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Abstract

Objective

In this study, our objective was to present real-life data on the incidence of inflammatory bowel disease (IBD) among patients receiving secukinumab treatment.

Methods

The study consisted of 209 patients who had prior exposure to anti-tumor necrosis factor (TNF) or were biologically naive. Patients with a pre-existing history of IBD were excluded from the study.

Results

Of the 209 patients in the study, 176 (84.3%) had ankylosing spondylitis, while 33 (15.7%) had psoriatic arthritis. 112 (53.6%) patients had prior exposure to at least one anti-TNF treatment before initiating secukinumab. IBD developed in 10 (4.8%) of the 209 patients. The incidence of IBD among patients who initiated secukinumab as their first biologic agent was 1%. For patients who had previously received any anti-TNF treatment and subsequently transitioned to secukinumab, the incidence of IBD was 8% (p = 0.018, odds ratio (OR): 8.38, 95% CI: 1.04–67.45). A mean of 3.67 months (±4.3) after anti-TNF use, whereas IBD symptoms developed in the biologically naive patient after 15 months.

Conclusion

Our study observed IBD incidence in 4.8% of patients using secukinumab. Patients who initiated secukinumab after previous anti-TNF treatment exhibited a significantly higher rate and risk of developing IBD. The onset of IBD occurred earlier in these patients (mean 3.67 months), whereas a single case of IBD showed a longer duration (15 months). Further studies with larger patient numbers are warranted to provide a more comprehensive understanding of our findings.

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抗肿瘤坏死因子治疗后使用secukinumab是否会增加患炎症性肠病的风险?
目的在这项研究中,我们的目的是提供有关接受secukinumab治疗的患者中炎症性肠病(IBD)发病率的真实数据。在209名患者中,176人(84.3%)患有强直性脊柱炎,33人(15.7%)患有银屑病关节炎。112名(53.6%)患者在开始使用secukinumab前至少接受过一种抗肿瘤坏死因子治疗。209名患者中有10人(4.8%)患上了IBD。在首次使用secukinumab作为生物制剂的患者中,IBD的发病率为1%。对于之前接受过任何抗肿瘤坏死因子治疗,随后转用secukinumab的患者,IBD发病率为8%(p = 0.018,几率比(OR):8.38,95% CI:1.04-67.45)。使用抗肿瘤坏死因子后平均3.67个月(±4.3),而生物幼稚型患者在15个月后才出现IBD症状。既往接受过抗 TNF 治疗后再开始使用 secukinumab 的患者患 IBD 的比例和风险明显更高。这些患者的 IBD 发病时间较早(平均 3.67 个月),而一例 IBD 病例的病程较长(15 个月)。为了更全面地了解我们的研究结果,有必要对更多的患者进行进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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