Characterization and Outcomes in Patients Treated With Apremilast in Routine Clinical Practice in Spain: Results From the APPRECIATE Study.

dc.contributor.authorHerranz, P
dc.contributor.authorTrasobares, L
dc.contributor.authorMateu, A
dc.contributor.authorMartínez, E
dc.contributor.authorRuiz-Villaverde, R
dc.contributor.authorBaniandrés, O
dc.contributor.authorMataix Díaz, J
dc.contributor.authorJiménez-Gómez, N
dc.contributor.authorSerra, M
dc.contributor.authorRuiz Genao, D P
dc.contributor.authorRivera, N
dc.contributor.authorTercedor-Sánchez, J
dc.contributor.authorGarcia, C
dc.contributor.authorCordey, M
dc.contributor.authorHerrera-Acosta, E
dc.date.accessioned2025-01-07T14:08:50Z
dc.date.available2025-01-07T14:08:50Z
dc.date.issued2021-05-27
dc.description.abstractIt is necessary to expand the knowledge in the use of apremilast in clinical practice. The APPRECIATE study (NCT02740218) aims to describe the characteristics of patients with psoriasis treated with apremilast, to evaluate their perspectives and those of dermatologists, as well as the outcomes obtained in clinical practice in Spain. Observational, retrospective, cross-sectional, multicenter study of patients with chronic plaque psoriasis who could be contacted 6 (±1) months after apremilast initiation. The data were obtained from medical records and questionnaires from patients and physicians. A total of 80 patients were evaluated; at apremilast onset, they showed mean (standard deviation, SD) Psoriasis Area and Severity Index (PASI) = 8.3 (5.3), mean (SD) Dermatology Life Quality Index (DLQI) = 8.9 (6.6). At six months, 58.8% (n=47) of patients continued apremilast treatment (discontinuations due to lack of efficacy [16.3%], safety/tolerability [20.0%]). In patients continuing treatment, PASI75 was achieved by 36.7% of patients; mean (95% CI) DLQI score was 2.2 (0.7-3.6) and mean (SD) Patient Benefit Index score was 2.8 (0.8). Compliance with physicians' expectations was correlated with benefits reported by patients (r=0.636). Adverse events were reported by 56.3% of patients (the most common were diarrhoea and nausea). Patients receiving apremilast for 6 months in Spanish clinical practice, reported substantial improvements in their quality of life (mean DLQI reduced by more than 6 points) and disease severity (PASI75 achieved by over one-third of patients), despite less skin involvement than patients who enrolled in clinical trials.
dc.identifier.doi10.1016/j.ad.2021.05.010
dc.identifier.essn2173-5778
dc.identifier.pmid34052202
dc.identifier.unpaywallURLhttps://doi.org/10.1016/j.ad.2021.05.010
dc.identifier.urihttps://hdl.handle.net/10668/26179
dc.journal.titleActas dermo-sifiliograficas
dc.journal.titleabbreviationActas Dermosifiliogr (Engl Ed)
dc.language.isoen
dc.language.isoes
dc.organizationSAS - Hospital Universitario San Cecilio
dc.organizationSAS - Hospital Universitario Virgen de las Nieves
dc.organizationSAS - Hospital Universitario San Cecilio
dc.pubmedtypeJournal Article
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectApremilast
dc.subjectBeneficios terapéuticos
dc.subjectClinical practice
dc.subjectPráctica clínica
dc.subjectPsoriasis
dc.subjectTherapeutic benefits
dc.titleCharacterization and Outcomes in Patients Treated With Apremilast in Routine Clinical Practice in Spain: Results From the APPRECIATE Study.
dc.title.alternativeCaracterización y resultados de pacientes tratados con apremilast en la práctica clínica habitual española: resultados del estudio APPRECIATE.
dc.typeresearch article
dc.type.hasVersionVoR

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