TY - JOUR
T1 - A snapshot on the on-label and off-label use of the interleukin-1 inhibitors in Italy among rheumatologists and pediatric rheumatologists: a nationwide multi-center retrospective observational study
AU - Vitale, Antonio
AU - Insalaco, Antonella
AU - Sfriso, Paolo
AU - Lopalco, Giuseppe
AU - Emmi, Giacomo
AU - Cattalini, Marco
AU - Manna, Raffaele
AU - Cimaz, Rolando
AU - Priori, Roberta
AU - Talarico, Rosaria
AU - Gentileschi, Stefano
AU - De Marchi, Ginevra
AU - Frassi, Micol
AU - Gallizzi, Romina
AU - Soriano, Alessandra
AU - Alessio, Maria
AU - Cammelli, Daniele
AU - Maggio, Maria C.
AU - Marcolongo, Renzo
AU - La Torre, Francesco
AU - Fabiani, Claudia
AU - Colafrancesco, Serena
AU - Ricci, Francesca
AU - Galozzi, Paola
AU - Viapiana, Ombretta
AU - Verrecchia, Elena
AU - Pardeo, Manuela
AU - Cerrito, Lucia
AU - Cavallaro, Elena
AU - Olivieri, Alma N.
AU - Paolazzi, Giuseppe
AU - Vitiello, Gianfranco
AU - Maier, Armin
AU - Silvestri, Elena
AU - Stagnaro, Chiara
AU - Valesini, Guido
AU - Mosca, Marta
AU - De Vita, Salvatore
AU - Tincani, Angela
AU - Lapadula, Giovanni
AU - Frediani, Bruno
AU - De Benedetti, Fabrizio
AU - Iannone, Florenzo
AU - Punzi, Leonardo
AU - Salvarani, Carlo
AU - Galeazzi, Mauro
AU - Rigante, Donato
AU - Cantarini, Luca
PY - 2016
Y1 - 2016
N2 - Background: Interleukin (IL)-1 inhibitors have been suggested as possible therapeutic options in a large number of old and new clinical entities characterized by an IL-1 driven pathogenesis. Objectives: To perform a nationwide snapshot of the on-label and off-label use of anakinra (ANA) and canakinumab (CAN) for different conditions both in children and adults. Methods: We retrospectively collected demographic, clinical, and therapeutic data from both adult and pediatric patients treated with IL-1 inhibitors from January 2008 to July 2016. Results: Five hundred and twenty-six treatment courses given to 475 patients (195 males, 280 females; 111 children and 364 adults) were evaluated. ANA was administered in 421 (80.04%) courses, CAN in 105 (19.96%). Sixty-two (32.1%) patients had been treated with both agents. IL-1 inhibitors were employed in 38 different indications (37 with ANA, 16 with CAN). Off-label use was more frequent for ANA than CAN (p < 0.0001). ANA was employed as first-line biologic approach in 323 (76.7%) cases, while CAN in 37 cases (35.2%). IL-1 inhibitors were associated with corticosteroids in 285 (54.18%) courses and disease modifying anti-rheumatic drugs (DMARDs) in 156 (29.65%). ANA dosage ranged from 30 to 200 mg/day (or 1.0-2.0 mg/kg/day) among adults and 2-4 mg/kg/day among children; regarding CAN, the most frequently used posologies were 150mg every 8 weeks, 150mg every 4 weeks and 150mg every 6 weeks. The frequency of failure was higher among patients treated with ANA at a dosage of 100 mg/day than those treated with 2 mg/kg/day (p = 0.03). Seventy-six patients (14.4%) reported an adverse event (AE) and 10 (1.9%) a severe AE. AEs occurred more frequently after the age of 65 compared to both children and patients aged between 16 and 65 (p = 0.003 and p = 0.03, respectively). Conclusions: IL-1 inhibitors are mostly used off-label, especially ANA, during adulthood. The high frequency of good clinical responses suggests that IL-1 inhibitors are used with awareness of pathogenetic mechanisms; adult healthcare physicians generally employ standard dosages, while pediatricians are more prone in using a weight-based posology. Dose adjustments and switching between different agents showed to be effective treatment strategies. Our data confirm the good safety profile of IL-1 inhibitors.
AB - Background: Interleukin (IL)-1 inhibitors have been suggested as possible therapeutic options in a large number of old and new clinical entities characterized by an IL-1 driven pathogenesis. Objectives: To perform a nationwide snapshot of the on-label and off-label use of anakinra (ANA) and canakinumab (CAN) for different conditions both in children and adults. Methods: We retrospectively collected demographic, clinical, and therapeutic data from both adult and pediatric patients treated with IL-1 inhibitors from January 2008 to July 2016. Results: Five hundred and twenty-six treatment courses given to 475 patients (195 males, 280 females; 111 children and 364 adults) were evaluated. ANA was administered in 421 (80.04%) courses, CAN in 105 (19.96%). Sixty-two (32.1%) patients had been treated with both agents. IL-1 inhibitors were employed in 38 different indications (37 with ANA, 16 with CAN). Off-label use was more frequent for ANA than CAN (p < 0.0001). ANA was employed as first-line biologic approach in 323 (76.7%) cases, while CAN in 37 cases (35.2%). IL-1 inhibitors were associated with corticosteroids in 285 (54.18%) courses and disease modifying anti-rheumatic drugs (DMARDs) in 156 (29.65%). ANA dosage ranged from 30 to 200 mg/day (or 1.0-2.0 mg/kg/day) among adults and 2-4 mg/kg/day among children; regarding CAN, the most frequently used posologies were 150mg every 8 weeks, 150mg every 4 weeks and 150mg every 6 weeks. The frequency of failure was higher among patients treated with ANA at a dosage of 100 mg/day than those treated with 2 mg/kg/day (p = 0.03). Seventy-six patients (14.4%) reported an adverse event (AE) and 10 (1.9%) a severe AE. AEs occurred more frequently after the age of 65 compared to both children and patients aged between 16 and 65 (p = 0.003 and p = 0.03, respectively). Conclusions: IL-1 inhibitors are mostly used off-label, especially ANA, during adulthood. The high frequency of good clinical responses suggests that IL-1 inhibitors are used with awareness of pathogenetic mechanisms; adult healthcare physicians generally employ standard dosages, while pediatricians are more prone in using a weight-based posology. Dose adjustments and switching between different agents showed to be effective treatment strategies. Our data confirm the good safety profile of IL-1 inhibitors.
KW - Interleukin-1 inhibitors
KW - Interleukin-1 inhibitors
UR - http://hdl.handle.net/10807/87359
U2 - 10.3389/fphar.2016.00380
DO - 10.3389/fphar.2016.00380
M3 - Article
SN - 1663-9812
VL - 2016
SP - 1
EP - 10
JO - Frontiers in Pharmacology
JF - Frontiers in Pharmacology
ER -