Department of Medical Sciences, Section of Dermatology, University of Turin, Turin, Italy.
Clinica Dermatologica Ospedale Policlinico San Martino - IRCCS, Università di Genova, Genova, Italy.
Expert Opin Biol Ther. 2024 Mar;24(3):133-138. doi: 10.1080/14712598.2024.2325547. Epub 2024 Mar 5.
The introduction of biologics for the treatment of plaque psoriasis is one of the major therapeutic advances of the last decades in dermatology. The efficacy of this class of drugs can be influenced by multiple factors including obesity, being overweight, prior treatment failures, and disease severity.
Most of the currently available approved biologics are limited by their lack of dosing flexibility for adapting the therapy to the complexity of real-world patients with psoriasis. Among the class of anti-interleukin-23, tildrakizumab allows a greater dosing flexibility, increasing clinical benefits of patients with high burden of the disease or body weight >90 kg.
This meta-opinion discusses the clinical data that were foundational for tildrakizumab dosage flexibility, elaborates on the definition of high burden of disease specifically linked to tildrakizumab dosage, and profiles the ideal patient that could benefit from treatment with the higher approved tildrakizumab dosage of 200 mg.
生物制剂的引入是过去几十年皮肤科治疗领域的重大进展之一,用于治疗斑块状银屑病。这类药物的疗效可能受到多种因素的影响,包括肥胖、超重、既往治疗失败和疾病严重程度。
目前大多数已批准的生物制剂都存在局限性,缺乏剂量灵活性,无法根据银屑病患者的实际情况调整治疗方案。在抗白细胞介素-23 类药物中,替度鲁单抗的剂量更灵活,为疾病负担重或体重超过 90 公斤的患者带来了更大的临床获益。
本综述性观点讨论了替度鲁单抗剂量灵活性的临床数据基础,阐述了与替度鲁单抗剂量相关的疾病高负担的定义,并描述了能从更高剂量(200mg)替度鲁单抗治疗中获益的理想患者。