TY - JOUR
T1 - Secukinumab Exhibits Sustained and Stable Response in Patients with Moderate-to-Severe Psoriasis: Results from the SUPREME Study
AU - Costanzo, Antonio
AU - Russo, Filomena
AU - Galluzzo, Marco
AU - Stingeni, Luca
AU - Scuderi, Roberta
AU - Zichichi, Leonardo
AU - Papini, Manuela
AU - Di Costanzo, Luisa
AU - Conti, Andrea
AU - Burlando, Martina
AU - Chiricozzi, Andrea
AU - Gaiani, Francesca Maria
AU - Mugheddu, Cristina
AU - Musumeci, Maria Letizia
AU - Gisondi, Paolo
AU - Piaserico, Stefano
AU - Dapavo, Paolo
AU - Venturini, Marina
AU - Pagnanelli, Gianluca
AU - Amerio, Paolo
AU - Potenza, Concetta
AU - Peris, Ketty
AU - Cantoresi, Franca
AU - Trevisini, Sara
AU - Loconsole, Francesco
AU - Offidani, Annamaria
AU - Mercuri, Santo Raffaele
AU - Lora, Viviana
AU - Prignano, Francesca
AU - Bartezaghi, Marta
AU - Oliva, Giovanni
AU - Aloisi, Elisabetta
AU - Orsenigo, Roberto
PY - 2021
Y1 - 2021
N2 - Secukinumab, a fully human monoclonal antibody, neutralizes interleukin-17A, a cornerstone cytokine driving the multiple manifestations of psoriasis. This post-hoc analysis of the SUPREME study was performed to determine the sustainability of response to secukinumab in terms of Psoriasis Area and Severity Index (PASI) 90 in patients with moderate-to-severe plaque psoriasis. Based on PASI 90 response at week 16, patients were stratified as PASI 90 responders (PASI90R, n = 337) or non-responders (PASI90NR, n = 72). At week 20, 94.2% (n = 295/313) achieved PASI 90/100 response in PASI90R, with response maintained through week 48 (89.6%, n = 189/211). An increased proportion of patients achieved PASI 90/100 response in PASI90NR (week 20: 29.9%, n = 20/67; week 48: 57.1%, n = 20/35). Overall, 64.4% patients achieved absolute PASI score = 0 at week 24 with response sustained to week 48 (66.9%). Secukinumab showed sustained and stable efficacy in maintaining PASI 90 response in patients with moderate-to-severe plaque psoriasis up to week 48.
AB - Secukinumab, a fully human monoclonal antibody, neutralizes interleukin-17A, a cornerstone cytokine driving the multiple manifestations of psoriasis. This post-hoc analysis of the SUPREME study was performed to determine the sustainability of response to secukinumab in terms of Psoriasis Area and Severity Index (PASI) 90 in patients with moderate-to-severe plaque psoriasis. Based on PASI 90 response at week 16, patients were stratified as PASI 90 responders (PASI90R, n = 337) or non-responders (PASI90NR, n = 72). At week 20, 94.2% (n = 295/313) achieved PASI 90/100 response in PASI90R, with response maintained through week 48 (89.6%, n = 189/211). An increased proportion of patients achieved PASI 90/100 response in PASI90NR (week 20: 29.9%, n = 20/67; week 48: 57.1%, n = 20/35). Overall, 64.4% patients achieved absolute PASI score = 0 at week 24 with response sustained to week 48 (66.9%). Secukinumab showed sustained and stable efficacy in maintaining PASI 90 response in patients with moderate-to-severe plaque psoriasis up to week 48.
KW - PASI 90
KW - interleukin-17A
KW - psoriasis
KW - secukinumab
KW - PASI 90
KW - interleukin-17A
KW - psoriasis
KW - secukinumab
UR - http://hdl.handle.net/10807/197485
U2 - 10.2340/00015555-3816
DO - 10.2340/00015555-3816
M3 - Article
SN - 1651-2057
VL - 101
SP - adv00576-N/A
JO - Acta Dermato-Venereologica
JF - Acta Dermato-Venereologica
ER -