Interleukin-13 Inhibitors in the Treatment of Atopic Dermatitis: The Role of Tralokinumab.

IF 2.5 4区 医学 Q2 DERMATOLOGY Dermatology practical & conceptual Pub Date : 2024-07-01 DOI:10.5826/dpc.1403a204
Annunziata Dattola, Martina Tolone, Emanuele Amore, Luigi Bennardo, Federica Trovato, Simone Amato, Teresa Grieco, Antonio Giovanni Richetta, Giovanni Pellacani, Nevena Skroza, Steven Paul Nisticò
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Abstract

Introduction: The advent of biotechnological drugs has significantly changed the management of atopic dermatitis (AD) and the approach to the moderate-to-severe form of this chronic relapsing disease.

Objectives: The aim of our review is to summarize the current literature on anti-interleukin (IL)-13 in atopic dermatitis.

Methods: A literature search was organized and a systematic review was performed to summarize the most recent evidence supporting the efficacy and safety of tralokinumab.

Results: Tralokinumab (anti-IL-13) 300 mg every 2 weeks subcutaneously has proven effective in several clinical trials in adults and adolescents with moderate to severe atopic dermatitis inadequately controlled with other topical or systemic therapies. Tralokinumab was found to be significantly superior in terms of efficacy in reducing Investigator's Global Assessment (IGA), Eczema Area and Severity Index (EASI) -75, Numeric Pain Rating Scale (NRS) pruritus, and Dermatology Life Quality Index (DLQI) scale numbers. During follow-up, tralokinumab was well tolerated with limited severity of adverse events.

Conclusions: Tralokinumab leads to statistically significant improvements in disease severity and outcome scores. It represents an effective treatment option for adults with moderate to severe AD, but further large-scale studies are needed to verify long-term superiority over other treatments.

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治疗特应性皮炎的白细胞介素-13 抑制剂:特罗凯单抗的作用。
简介:生物技术药物的出现极大地改变了特应性皮炎(AD)的治疗方法以及这种慢性复发性疾病的中重度治疗方法:我们的综述旨在总结有关抗白细胞介素(IL)-13治疗特应性皮炎的现有文献:方法:组织文献检索并进行系统综述,总结支持曲洛单抗有效性和安全性的最新证据:特罗凯单抗(抗IL-13)300 毫克,每两周皮下注射一次,已在几项临床试验中证明对其他局部或全身疗法控制不佳的中重度特应性皮炎成人和青少年患者有效。研究发现,曲妥珠单抗在降低研究者总体评估(IGA)、湿疹面积和严重程度指数(EASI)-75、数字疼痛评分量表(NRS)瘙痒程度和皮肤科生活质量指数(DLQI)方面的疗效显著优于其他药物。在随访期间,曲洛单抗的耐受性良好,不良反应的严重程度有限:结论:曲妥珠单抗可在统计学上显著改善疾病的严重程度和疗效评分。结论:曲妥珠单抗能在统计学上显著改善疾病的严重程度和结果评分,是中重度成人注意力缺失症患者的有效治疗选择,但还需要进一步的大规模研究来验证其长期疗效优于其他治疗方法。
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