TY - JOUR
T1 - Brodalumab for the Treatment of Moderate-to-Severe Psoriasis: An Expert Delphi Consensus Statement
AU - Fargnoli, Maria Concetta
AU - Bardazzi, Federico
AU - Bianchi, Luca
AU - Dapavo, Paolo
AU - Fabbrocini, Gabriella
AU - Gisondi, Paolo
AU - Micali, Giuseppe
AU - Offidani, Anna Maria
AU - Pellacani, Giovanni
AU - Skroza, Nevena
AU - Angileri, Rosa Giuseppa
AU - Burlando, Martina
AU - Campanati, Anna
AU - Carrera, Carlo Giovanni
AU - Chiricozzi, Andrea
AU - Conti, Andrea
AU - De Simone, Clara
AU - Di Lernia, Vito
AU - Errichetti, Enzo
AU - Galluzzo, Marco
AU - Guarneri, Claudio
AU - Lasagni, Claudia
AU - Lembo, Serena
AU - Loconsole, Francesco
AU - Megna, Matteo
AU - Musumeci, Maria Letizia
AU - Prignano, Francesca
AU - Richetta, Antonio Giovanni
AU - Trovato, Emanuele
AU - Venturini, Marina
AU - Peris, Ketty
AU - Pinton, Piergiacomo Calzavara
PY - 2023
Y1 - 2023
N2 - Brodalumab is a recombinant, fully human immunoglobulin IgG2 monoclonal antibody specifically targeted against interleukin-17RA that has been approved for the treatment of moderate-to-severe psoriasis in Europe. We developed a Delphi consensus document focused on brodalumab for the treatment of moderate-to-severe psoriasis. Based on published literature and their clinical experience a steering committee drafted 17 statements covering 7 domains specific to the treatment of moderate-to-severe psoriasis with brodalumab. A panel of 32 Italian dermatologists indicated their level of agreement using a 5-point Likert scale (from 1 = “strongly disagree” to 5 = “strongly agree”) using an online modified Delphi method. After the first round of voting (32 participants), positive consensus was reached for 15/17 (88.2%) of the proposed statements. Following a face-to-face virtual meeting, the steering committee decided that 5 statements would form “main principles” and 10 statements formed the final list. After a second round of voting, consensus was reached in 4/5 (80%) of the main principles and 8/10 (80%) for consensus statements. The final list of 5 main principles and 10 consensus statements identify key indications specific to the use of brodalumab in the treatment of moderate-to-severe psoriasis in Italy. These statements aid dermatologists in the management of patients with moderate-to-severe psoriasis.
AB - Brodalumab is a recombinant, fully human immunoglobulin IgG2 monoclonal antibody specifically targeted against interleukin-17RA that has been approved for the treatment of moderate-to-severe psoriasis in Europe. We developed a Delphi consensus document focused on brodalumab for the treatment of moderate-to-severe psoriasis. Based on published literature and their clinical experience a steering committee drafted 17 statements covering 7 domains specific to the treatment of moderate-to-severe psoriasis with brodalumab. A panel of 32 Italian dermatologists indicated their level of agreement using a 5-point Likert scale (from 1 = “strongly disagree” to 5 = “strongly agree”) using an online modified Delphi method. After the first round of voting (32 participants), positive consensus was reached for 15/17 (88.2%) of the proposed statements. Following a face-to-face virtual meeting, the steering committee decided that 5 statements would form “main principles” and 10 statements formed the final list. After a second round of voting, consensus was reached in 4/5 (80%) of the main principles and 8/10 (80%) for consensus statements. The final list of 5 main principles and 10 consensus statements identify key indications specific to the use of brodalumab in the treatment of moderate-to-severe psoriasis in Italy. These statements aid dermatologists in the management of patients with moderate-to-severe psoriasis.
KW - Delphi
KW - brodalumab
KW - consensus
KW - psoriasis
KW - statement
KW - Delphi
KW - brodalumab
KW - consensus
KW - psoriasis
KW - statement
UR - http://hdl.handle.net/10807/249134
U2 - 10.3390/jcm12103545
DO - 10.3390/jcm12103545
M3 - Article
SN - 2077-0383
VL - 12
SP - 3545-N/A
JO - Journal of Clinical Medicine
JF - Journal of Clinical Medicine
ER -