TY - JOUR
T1 - 2-Year Experience with Risankizumab in the Treatment of Plaque Psoriasis in Lazio Region, Italy
AU - Caldarola, Giacomo
AU - De Luca, Eleonora
AU - Bavetta, Mauro
AU - Bernardini, Nicoletta
AU - Dattola, Annunziata
AU - Dattola, Carmelo Alberto
AU - De Simone, Clara
AU - Gracefa, Dario
AU - Bonifati, Claudio
AU - Tribuzi, Paola
AU - Giordano, Domenico
AU - Mariani, Marco
AU - Moretta, Gaia
AU - Pagnanelli, Gianluca
AU - Panasiti, Vincenzo
AU - Provini, Alessia
AU - Richetta, Antonio
AU - Zangrilli, Arianna
AU - Bianchi, Luca
AU - Pellacani, Giovanni
AU - Peris, Ketty
PY - 2023
Y1 - 2023
N2 - Background. Given the chronic relapsing, remitting course of psoriasis, data about long-term efectiveness may be useful to assess the maintenance of clinical response over time. Objective. To evaluate 2-year drug survival of risankizumab and identify any predictive factor of discontinuation for inefectiveness. Materials and Methods. A multicenter retrospective study was conducted in patients who initiated risankizumab between July 2019 and December 2020. PASI was measured at baseline and after 104 weeks. Any adverse event was registered during visits. Univariable and multivariable logistic regressions were used to assess baseline patients’ characteristics that predicted clinical response. Te drug survival analysis was descriptively performed using the Kaplan–Meier survival curve. Results. 112 patients with moderate-to-severe plaque psoriasis were included. Te overall median observation time was 35.3 months (26.7–37.3); the estimated survivor cumulative function at months 12 and 24 was 93.6% and 90.6%, respectively. No diferences in BMI, disease duration, disease severity, or previous biological therapies were observed in patients who responded or did not respond to treatment. No signifcant adverse events were reported, but there was relapse of psoriatic arthritis and ulcerative colitis in a patient. Conclusions. We found that risankizumab was associated with long-term efectiveness, and a favorable safety profle in a population of psoriatic patients was observed, over a period of 2 years.
AB - Background. Given the chronic relapsing, remitting course of psoriasis, data about long-term efectiveness may be useful to assess the maintenance of clinical response over time. Objective. To evaluate 2-year drug survival of risankizumab and identify any predictive factor of discontinuation for inefectiveness. Materials and Methods. A multicenter retrospective study was conducted in patients who initiated risankizumab between July 2019 and December 2020. PASI was measured at baseline and after 104 weeks. Any adverse event was registered during visits. Univariable and multivariable logistic regressions were used to assess baseline patients’ characteristics that predicted clinical response. Te drug survival analysis was descriptively performed using the Kaplan–Meier survival curve. Results. 112 patients with moderate-to-severe plaque psoriasis were included. Te overall median observation time was 35.3 months (26.7–37.3); the estimated survivor cumulative function at months 12 and 24 was 93.6% and 90.6%, respectively. No diferences in BMI, disease duration, disease severity, or previous biological therapies were observed in patients who responded or did not respond to treatment. No signifcant adverse events were reported, but there was relapse of psoriatic arthritis and ulcerative colitis in a patient. Conclusions. We found that risankizumab was associated with long-term efectiveness, and a favorable safety profle in a population of psoriatic patients was observed, over a period of 2 years.
KW - eczmema
KW - eczmema
UR - http://hdl.handle.net/10807/261984
U2 - 10.1155/2023/9832296
DO - 10.1155/2023/9832296
M3 - Article
SN - 1396-0296
VL - 2023
SP - 1
EP - 6
JO - Dermatologic Therapy
JF - Dermatologic Therapy
ER -