Identificador persistente para citar o vincular este elemento: https://accedacris.ulpgc.es/handle/10553/136255
Campo DC Valoridioma
dc.contributor.authorAbad, Maria Reyes-
dc.contributor.authorAlerany, Carmen-
dc.contributor.authorGonzalez, Luis Ignacio-
dc.contributor.authorNeth, Olaf-
dc.contributor.authorPayares-Herrera, Concepcion-
dc.contributor.authorRodríguez-Gallego, Carlos-
dc.contributor.authorTrillo, Jose Luis-
dc.contributor.authorHerrmann, Kirsten H.-
dc.contributor.authorFigueiredo, Raquel-
dc.contributor.authorGil, Alicia-
dc.date.accessioned2025-02-17T12:54:18Z-
dc.date.available2025-02-17T12:54:18Z-
dc.date.issued2025-
dc.identifier.issn2284-2403-
dc.identifier.otherWoS-
dc.identifier.urihttps://accedacris.ulpgc.es/handle/10553/136255-
dc.description.abstractBackground: Activated phosphoinositide 3-kinase (PI3K) delta Syndrome (APDS) is an ultra-rare, potentially life- threatening disease that lacks approved treatments in Spain. This study aimed to apply Multi-Criteria Decision Analysis (MCDA) to assess the value of the first pharmacological treatment for APDS in Spain. Methods: A multidisciplinary group of 8 experts evaluated the selective PI3K delta inhibitor leniolisib against Standard of Care (SoC). An MCDA framework tailored for Orphan Drugs (ODs), consisting of 5 comparative and 2 quantitative non-comparative criteria, was used. Re-scoring followed a group discussion. Results: Leniolisib scored higher than SoC in all criteria, including efficacy and safety. It was deemed highly valuable as the first disease-modifying treatment, with a positive therapeutic impact and potential to improve patients' quality of life. Additionally, leniolisib may lead to cost savings. The supporting data was considered of high quality. Conclusion: Based on MCDA methodology and stakeholder experience in APDS management, leniolisib is seen as a value-added treatment option compared to SoC in Spain.-
dc.languagespa-
dc.relation.ispartofGlobal and Regional Health Technology Assessment-
dc.sourceGlobal & Regional Health Technology Assessment [ISSN 2284-2403], v. 12, p. 9-15, (Enero 2025)-
dc.subject320505 Enfermedades infecciosas-
dc.subject320990 Farmacología experimental-
dc.subject.otherHuman Immunodeficiency-
dc.subject.otherCriteria-
dc.subject.otherPi3K-
dc.subject.otherFramework-
dc.subject.otherTherapy-
dc.subject.otherActivated Phosphoinositide 3-Kinase (Pi3K) Delta Syndrome (Apds)-
dc.subject.otherDecision-Making-
dc.subject.otherMulti-Criteria Deci Sion Analysis (Mcda)-
dc.subject.otherUltra-Rare Disease-
dc.subject.otherLeniolisib-
dc.titleValue contribution of leniolisib in the Treatment of Activated PI3Kδ syndrome (APDS) in Spain using Multi-Criteria Decision Analysis (MCDA)-
dc.typeinfo:eu-repo/semantics/Article-
dc.typeArticle-
dc.identifier.doi10.33393/grhta.2025.3199-
dc.identifier.scopus85216871952-
dc.identifier.isi001412560800001-
dc.contributor.orcid0000-0001-5527-9668-
dc.contributor.orcidNO DATA-
dc.contributor.orcid0000-0001-6917-8980-
dc.contributor.orcidNO DATA-
dc.contributor.orcid0009-0001-7041-1564-
dc.contributor.orcidNO DATA-
dc.contributor.orcidNO DATA-
dc.contributor.orcid0000-0002-9701-2854-
dc.contributor.orcid0009-0009-3029-6600-
dc.contributor.orcid0000-0003-3006-7858-
dc.contributor.authorscopusid55412223700-
dc.contributor.authorscopusid6603480107-
dc.contributor.authorscopusid59540742600-
dc.contributor.authorscopusid6506737455-
dc.contributor.authorscopusid57200648111-
dc.contributor.authorscopusid6602114379-
dc.contributor.authorscopusid36697104100-
dc.contributor.authorscopusid57194337919-
dc.contributor.authorscopusid59154088500-
dc.contributor.authorscopusid57205020346-
dc.identifier.eissn2283-5733-
dc.description.lastpage15-
dc.identifier.issue1-
dc.description.firstpage9-
dc.relation.volume12-
dc.investigacionCiencias de la Salud-
dc.type2Artículo-
dc.contributor.daisngidNo ID-
dc.contributor.daisngidNo ID-
dc.contributor.daisngidNo ID-
dc.contributor.daisngidNo ID-
dc.contributor.daisngidNo ID-
dc.contributor.daisngidNo ID-
dc.contributor.daisngidNo ID-
dc.contributor.daisngidNo ID-
dc.contributor.daisngidNo ID-
dc.contributor.daisngidNo ID-
dc.description.numberofpages7-
dc.utils.revisionNo-
dc.contributor.wosstandardWOS:Abad, MR-
dc.contributor.wosstandardWOS:Alerany, C-
dc.contributor.wosstandardWOS:González, LI-
dc.contributor.wosstandardWOS:Neth, O-
dc.contributor.wosstandardWOS:Payares-Herrera, C-
dc.contributor.wosstandardWOS:Rodríguez-Gallego, C-
dc.contributor.wosstandardWOS:Trillo, JL-
dc.contributor.wosstandardWOS:Herrmann, KH-
dc.contributor.wosstandardWOS:Figueiredo, R-
dc.contributor.wosstandardWOS:Gil, A-
dc.date.coverdateEnero 2025-
dc.identifier.ulpgc-
dc.contributor.buulpgcBU-MED-
dc.description.esciESCI-
item.fulltextCon texto completo-
item.grantfulltextopen-
crisitem.author.deptGIR IUIBS: Patología y Tecnología médica-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Ciencias Médicas y Quirúrgicas-
crisitem.author.orcid0000-0002-4344-8644-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameRodríguez Gallego, José Carlos-
Colección:Artículos
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