Switching from Secukinumab to Ustekinumab in Psoriasis Patients: Results from a Multicenter Experience

被引:11
|
作者
Chiricozzi, Andrea [1 ,2 ]
Conti, Andrea [3 ]
Burlando, Martina [4 ]
Odorici, Giulia [3 ]
Gaiani, Francesca [5 ]
Panduri, Salvatore [2 ]
Malagoli, Piergiorgio [5 ]
机构
[1] Catholic Univ, Inst Dermatol, Fdn Policlin Univ A Gemelli, IRCCS, Largo Agostino Gemelli 8, IT-00168 Rome, Italy
[2] Univ Pisa, Dept Clin & Expt Med, Dermatol Unit, Pisa, Italy
[3] Univ Policlin Modena, Dept Head & Neck Surg, Sect Dermatol, Azienda Osped, Modena, Italy
[4] Univ Genoa, Sect Dermatol, DiSSal, San Martino Policlin Hosp, Genoa, Italy
[5] Azienda Osped San Donato Milanese, Dermatol Unit, Milan, Italy
关键词
Psoriasis; Secukinumab; Ustekinumab; Switch; INTERLEUKIN-12/23; MONOCLONAL-ANTIBODY; DRUG SURVIVAL; BIOLOGIC AGENTS; INTESTINAL INFLAMMATION; LONGITUDINAL ASSESSMENT; PLAQUE PSORIASIS; DOUBLE-BLIND; EFFICACY; SAFETY; REGISTRY;
D O I
10.1159/000497274
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Switching between biologics is commonly performed for the management of plaque psoriasis. However, no evidence about switching from secukinumab to ustekinumab has been reported. Methods: This retrospective observational multicenter study aimed to describe efficacy and safety of ustekinumab in secukinumab nonresponder patients. Results: A total of 21 patients unresponsive to secukinumab were treated with ustekinumab for a mean period of 53.3 weeks. Ustekinumab was effective in reducing disease severity, with significant improvements of both psoriasis area severity index (PASI) and dermatology quality of life index (DLQI) scores. PASI score improvements of 31.8, 44, 77.8, 80.3, 80.5, and 89.6%, at week 4, 12, 24, 36, 48, and above 60 weeks, respectively, were detected (p < 0.05), achieving PASI 50, 75, and >90 responses in 93.8, 87.5, and 50% of patients at week 48. Four patients withdrew from ustekinumab treatment because of inefficacy, and failure of multiple biologic agents (>2) seemed to affect ustekinumab drug survival. No serious adverse events (AEs) were reported while 38.1% of patients experienced mild AEs. Conclusion: Ustekinumab was safe and effective in treating patients un- responsive to secukinumab. (C) 2019 S. Karger AG, Basel
引用
收藏
页码:213 / 218
页数:6
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