TY - JOUR
T1 - Real-World Apremilast Use for Treatment of Plaque Psoriasis in Italy: Patient Perspective, Characteristics, and Clinical Outcomes from the DARWIN Study
AU - Giofre, C.
AU - Fabbrocini, G.
AU - Potenza, C.
AU - Tiberio, R.
AU - Gisondi, P.
AU - Marasca, C.
AU - Nuzzo, C. M. A.
AU - Benincasa, E.
AU - Bianchi, L.
AU - Dapavo, P.
AU - Parodi, A.
AU - Atzori, L.
AU - Pasquale, R.
AU - Peris, Ketty
AU - Amerio, P.
AU - Venturini, M.
AU - Schiavo, A. L.
AU - Romanelli, M.
AU - Richetta, A.
AU - Cusano, F.
AU - Fargnoli, M. C.
AU - Offidani, A.
AU - Guarneri, C.
AU - Prignano, F.
AU - Corazza, M.
AU - Bongiorno, M. R.
AU - Loconsole, F.
AU - Ori, A.
AU - Simoni, L.
AU - Amici, C.
AU - Palma, L. D.
AU - Andreis, D.
AU - Trevisan, F.
AU - Sala, S.
AU - Patane, R.
AU - Mele, F.
AU - Pernaci, A.
AU - Ruberti, S.
AU - Trogu, M.
AU - Pelicelli, S.
AU - Rizzoli, S.
PY - 2023
Y1 - 2023
N2 - Introduction: While several European studies have reported real-world apremilast use, patient-perceived benefits, and treatment satisfaction, local reimbursement criteria for apremilast vary and data from Italy are limited. Methods: The cross-sectional DARWIN study enrolled consecutive patients who had initiated apremilast for plaque psoriasis 6 (± 1) months prior to enrolment at a single visit across 24 Italian dermatological sites. Disease severity was assessed using body surface area (BSA) and Physician Global Assessment (PGA). Patient-reported outcomes assessed 6 (± 1) months after apremilast initiation were Dermatology Life Quality Index (DLQI), Patient Benefit Index (PBI), and 9-item Treatment Satisfaction Questionnaire for Medication (TSQM-9). Results: Of 184 patients enrolled between July 2019 and January 2021, 180 were included in the analysis. At apremilast initiation, median (25th–75th percentile) time since psoriasis diagnosis was 8.6 (3.2–22.2) years; median BSA, 10.0% (5.0–16.0); mean (standard seviation, SD) DLQI total score, 13.5 (8.0). Over half (54.9%) of patients with available data reported psoriasis had a very or extremely large effect on their quality of life (QoL); half reported itching (50.6%) and/or special areas involvement (50.0%). Most (73.9%) had comorbidities and were biologic-naïve (81.5%). The most common reasons for initiating apremilast were lack of efficacy of previous treatment (56.7%) and contraindications to other treatments (44.4%). At 6 (± 1) months, most patients were continuing apremilast and/or reported a Global PBI score ≥ 1 (minimum clinical benefit) (86.1% and 90.0%, respectively); approximately half achieved BSA ≤ 3% and/or DLQI total score ≤ 5 (47.1% and 48.5%); 18.8% achieved PGA = 0; mean (SD) TSQM-9 global treatment satisfaction score was 59.0 (24.8). Apremilast was well tolerated; no new safety signals were identified. Conclusions: Patients treated with apremilast for 6 months in Italian clinical practice reported improved QoL, clinically relevant improvements in symptoms, high treatment satisfaction, and high treatment persistence. Our data indicate apremilast is a valuable treatment option for moderate plaque psoriasis. Study Registration: ClinicalTrials.gov identifier, NCT04031027.
AB - Introduction: While several European studies have reported real-world apremilast use, patient-perceived benefits, and treatment satisfaction, local reimbursement criteria for apremilast vary and data from Italy are limited. Methods: The cross-sectional DARWIN study enrolled consecutive patients who had initiated apremilast for plaque psoriasis 6 (± 1) months prior to enrolment at a single visit across 24 Italian dermatological sites. Disease severity was assessed using body surface area (BSA) and Physician Global Assessment (PGA). Patient-reported outcomes assessed 6 (± 1) months after apremilast initiation were Dermatology Life Quality Index (DLQI), Patient Benefit Index (PBI), and 9-item Treatment Satisfaction Questionnaire for Medication (TSQM-9). Results: Of 184 patients enrolled between July 2019 and January 2021, 180 were included in the analysis. At apremilast initiation, median (25th–75th percentile) time since psoriasis diagnosis was 8.6 (3.2–22.2) years; median BSA, 10.0% (5.0–16.0); mean (standard seviation, SD) DLQI total score, 13.5 (8.0). Over half (54.9%) of patients with available data reported psoriasis had a very or extremely large effect on their quality of life (QoL); half reported itching (50.6%) and/or special areas involvement (50.0%). Most (73.9%) had comorbidities and were biologic-naïve (81.5%). The most common reasons for initiating apremilast were lack of efficacy of previous treatment (56.7%) and contraindications to other treatments (44.4%). At 6 (± 1) months, most patients were continuing apremilast and/or reported a Global PBI score ≥ 1 (minimum clinical benefit) (86.1% and 90.0%, respectively); approximately half achieved BSA ≤ 3% and/or DLQI total score ≤ 5 (47.1% and 48.5%); 18.8% achieved PGA = 0; mean (SD) TSQM-9 global treatment satisfaction score was 59.0 (24.8). Apremilast was well tolerated; no new safety signals were identified. Conclusions: Patients treated with apremilast for 6 months in Italian clinical practice reported improved QoL, clinically relevant improvements in symptoms, high treatment satisfaction, and high treatment persistence. Our data indicate apremilast is a valuable treatment option for moderate plaque psoriasis. Study Registration: ClinicalTrials.gov identifier, NCT04031027.
KW - Apremilast
KW - Dermatology Life Quality Index
KW - Italian real-world evidence
KW - Patient Benefit Index
KW - Patient perspective
KW - Patient-reported outcomes
KW - Plaque psoriasis
KW - Psoriasis comorbidities
KW - Quality of life
KW - Treatment satisfaction
KW - Apremilast
KW - Dermatology Life Quality Index
KW - Italian real-world evidence
KW - Patient Benefit Index
KW - Patient perspective
KW - Patient-reported outcomes
KW - Plaque psoriasis
KW - Psoriasis comorbidities
KW - Quality of life
KW - Treatment satisfaction
UR - https://publicatt.unicatt.it/handle/10807/249100
UR - https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85159558924&origin=inward
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85159558924&origin=inward
U2 - 10.1007/s12325-023-02516-y
DO - 10.1007/s12325-023-02516-y
M3 - Article
SN - 0741-238X
VL - 40
SP - 3021
EP - 3037
JO - Advances in Therapy
JF - Advances in Therapy
IS - 7
ER -