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老年银屑病患者的抗白细胞介素-23 治疗:真实世界中 Guselkumab、Risankizumab 和 Tildrakizumab 的应用。

Anti-interleukin-23 for psoriasis in elderly patients: guselkumab, risankizumab and tildrakizumab in real-world practice.

机构信息

Section of Dermatology, Department of Clinical Medicine and Surgery, University of Naples Federico II, Naples, Italy.

Department of Dermatology, University Hospital Dr José Eleuterio González, Universidad Autónoma de Nuevo León, Monterrey, Mexico.

出版信息

Clin Exp Dermatol. 2022 Mar;47(3):561-567. doi: 10.1111/ced.14979. Epub 2021 Nov 17.

Abstract

BACKGROUND

Elderly patients (aged ≥ 65 years) represent an increasing proportion of patients with psoriasis and 15% of these have moderate to severe disease. Biologics are being used frequently in this group of patients even though safety and efficacy data are limited. In addition, owing to anti-interleukin (IL)-23 therapies being a relatively recent option, no data have been reported about their use in elderly patients with psoriasis.

AIM

To evaluate and compare the safety and efficacy of guselkumab, risankizumab and tildrakizumab in real-world practice in elderly patients.

METHODS

This was a single-centre retrospective study that enrolled patients aged ≥ 65 years with moderate to severe plaque psoriasis, treated with guselkumab, risankizumab or tildrakizumab. The length of the study for each group depended on the drug (44 weeks for risankisumab, 40 weeks for guselkumab and 28 weeks for tildrakizumab, owing to its more recent availability in Italy).

RESULTS

In total, 34 patients were enrolled (n = 20 on guselkumab; n = 8 on risankizumab; n = 6 on tildrakizumab). At Week 4, 29.4% reached 90% improvement in Psoriasis Area and Severity Index (PASI90) and 8.8% reached 100% improvement in PASI (PASI100); at Week 28, PASI90 and PASI100 was reached by 58.8% and 29.4%, respectively. At the final follow-up (Week 40 or 44, depending on drug), data were available only for the risankizumab (Week 40) and guselkumab (Week 44) and groups, and showed that 71.4% of patients had reached PASI90 and 53.5% had reached PASI100. Four patients (11.7%) discontinued treatment. No significant differences were found between the three groups. The limitations of the study included its retrospective nature of the study, small sample size, and different numbers of patients and follow-up duration for the different groups (highest for guselkumab, lowest for tildrakizumab).

CONCLUSION

The three anti-IL-23 therapies assessed are promising, safe and effective options in elderly patients, and there was no significant difference between them. However, more data are needed to confirm our results and to understand their role in the management of this group of patients.

摘要

背景

老年患者(年龄≥65 岁)在银屑病患者中所占比例不断增加,其中 15%为中重度疾病患者。尽管生物制剂的安全性和有效性数据有限,但这类患者仍经常使用生物制剂。此外,由于抗白细胞介素(IL)-23 治疗是一种相对较新的选择,因此尚未报告其在老年银屑病患者中的使用情况。

目的

评估和比较 Guselkumab、Risankizumab 和 Tildrakizumab 在真实世界实践中用于老年患者的安全性和疗效。

方法

这是一项单中心回顾性研究,纳入了年龄≥65 岁、患有中重度斑块状银屑病、接受 Guselkumab、Risankizumab 或 Tildrakizumab 治疗的患者。每组的研究时间取决于药物(Risankizumab 为 44 周,Guselkumab 为 40 周,Tildrakizumab 为 28 周,因为它在意大利的供应时间较晚)。

结果

共纳入 34 例患者(Guselkumab 组 n=20;Risankizumab 组 n=8;Tildrakizumab 组 n=6)。在第 4 周,29.4%的患者达到了银屑病面积和严重程度指数(PASI90)的 90%改善,8.8%的患者达到了 PASI100 的改善;在第 28 周,分别有 58.8%和 29.4%的患者达到了 PASI90 和 PASI100。在最终随访(取决于药物,为第 40 周或第 44 周)时,仅获得了 Risankizumab(第 40 周)和 Guselkumab(第 44 周)组的数据,结果显示 71.4%的患者达到了 PASI90,53.5%的患者达到了 PASI100。有 4 例(11.7%)患者停止了治疗。三组之间未发现显著差异。研究的局限性包括研究的回顾性、样本量小,以及不同组别的患者数量和随访时间不同(Guselkumab 组最高,Tildrakizumab 组最低)。

结论

评估的三种抗 IL-23 疗法在老年患者中是有前景的、安全且有效的选择,且三者之间无显著差异。然而,需要更多的数据来证实我们的结果,并了解它们在治疗这类患者中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e26/9299162/cb8fcfd10b94/CED-47-561-g001.jpg

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