Nalazite se na CroRIS probnoj okolini. Ovdje evidentirani podaci neće biti pohranjeni u Informacijskom sustavu znanosti RH. Ako je ovo greška, CroRIS produkcijskoj okolini moguće je pristupi putem poveznice www.croris.hr
izvor podataka: crosbi !

Apremilast Use in Severe Psoriasis: Real-World Data from Central and Eastern Europe (CROSBI ID 322328)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Cetkovská, Petra ; Dediol, Iva ; Šola, Marija ; Kojanová, Martina ; Trčko, Katarina ; Čarija, Antoanela ; Čeović, Romana ; Ledić-Drvar, Daniela ; Kaštelan, Marija ; Hrabar, Andina Apremilast Use in Severe Psoriasis: Real-World Data from Central and Eastern Europe // Advances in therapy, - (2023), -, 16. doi: 10.1007/s12325-023-02468-3

Podaci o odgovornosti

Cetkovská, Petra ; Dediol, Iva ; Šola, Marija ; Kojanová, Martina ; Trčko, Katarina ; Čarija, Antoanela ; Čeović, Romana ; Ledić-Drvar, Daniela ; Kaštelan, Marija ; Hrabar, Andina

engleski

Apremilast Use in Severe Psoriasis: Real-World Data from Central and Eastern Europe

Introduction The broad and sustained efficacy of apremilast for psoriasis has been demonstrated in randomized and real-world observational studies. Data from Central and Eastern Europe (CEE) are lacking. Moreover, apremilast use in this region is limited by country-specific reimbursement criteria. This is the first study to report data on the real- world use of apremilast in the region. Methods APPRECIATE (NCT02740218) was an observational, retrospective, cross-sectional study assessing psoriasis patients 6 (± 1) months after apremilast treatment initiation. The study aimed to describe the characteristics of patients with psoriasis receiving apremilast, estimate treatment outcomes, including Psoriasis Area Severity Index (PASI), Body Surface Area (BSA), and Dermatology Life Quality Index (DLQI), and assess dermatologists' and patients' perspectives on treatment using questionnaires including the Patient Benefit Index (PBI). Adverse event reports were taken from the medical records. Results Fifty patients (Croatia: 25 ; Czech Republic: 20 ; Slovenia: 5) were enrolled. In patients continuing apremilast at 6 (± 1) months, mean (± SD) PASI score was reduced from 16.2 ± 8.7 points at treatment initiation to 3.1 ± 5.2 at 6 (± 1) months ; BSA from 11.9% ± 10.3% to 0.8% ± 0.9% ; DLQI from 13.7 ± 7.4 points to 1.6 ± 3.2. PASI 75 was reached by 81% of patients. Physicians reported that the overall treatment success fulfilled their expectations in more than two thirds of patients (68%). At least three-quarters of patients reported apremilast had a quite or very high benefit on the needs they identified as being most important. Apremilast was well tolerated ; no serious or fatal adverse events were identified. Conclusion Apremilast was effective in reducing skin involvement and improving quality of life in CEE patients having severe disease. Treatment satisfaction among physicians and patients was very high. These data add to the growing body of evidence showing consistent effectiveness of apremilast across the continuum of psoriasis disease severity and manifestations.

Apremilast ; Psoriasis drug therapy ; Real-world data ; Health-related quality of life ; Psoriasis severity scores

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

Podaci o izdanju

-

2023.

-

16

objavljeno

0741-238X

1865-8652

10.1007/s12325-023-02468-3

Povezanost rada

Temeljne medicinske znanosti

Poveznice
Indeksiranost