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dc.contributor.authorMartínez-Cuadrón, David
dc.contributor.authorMontesinos, Pau
dc.contributor.authorVellenga, Edo
dc.contributor.authorBernal, Teresa
dc.contributor.authorSalamero, Olga
dc.contributor.authorHolowiecka, Aleksandra
dc.contributor.authorBrunet, Salut
dc.contributor.authorGil, Cristina
dc.contributor.authorBenavente, Celina
dc.contributor.authorRibera, Josep Maria
dc.contributor.authorPérez Encinas, Manuel Mateo 
dc.contributor.authorde la Serna, Javier
dc.contributor.authorEsteve, Jordi
dc.contributor.authorRubio, Vicente
dc.contributor.authorGonzález-Campos, José
dc.contributor.authorEscoda, Lourdes
dc.contributor.authorAmutio, María Elena
dc.contributor.authorArnan, M.
dc.contributor.authorArias Sampedro, Jesús
dc.contributor.authorNegri, S.
dc.contributor.authorLowenberg, Bob
dc.contributor.authorSanz, Miguel A.
dc.date.accessioned2026-01-23T11:13:29Z
dc.date.available2026-01-23T11:13:29Z
dc.date.issued2018
dc.identifier.otherhttps://pubmed.ncbi.nlm.nih.gov/28584252/es
dc.identifier.urihttp://hdl.handle.net/20.500.11940/22461
dc.description.abstract[EN] Treatment outcome in older patients with acute promyelocytic leukemia (APL) is lower compared with younger patients, mainly because of a higher induction death rate and postremission non-relapse mortality (NRM). This prompted us to design a risk- and age-adapted protocol (Programa Español de Tratamientos en Hematología (PETHEMA)/HOVON LPA2005), with dose reduction of consolidation chemotherapy. Patients aged ⩾60 years reported to the PETHEMA registry and were treated with all-trans retinoic acid (ATRA) plus anthracycline-based regimens according to three consecutive PETHEMA trials that were included. We compared the long-term outcomes of the LPA2005 trial with the preceding PETHEMA trials using non-age-adapted schedules (LPA96&LPA99). From 1996 to 2012, 389 older patients were registered, of whom 268 patients (69%) were eligible. Causes of ineligibility were secondary APL (19%), and unfit for chemotherapy (11%). Median age was 67 years, without relevant differences between LPA2005 and LPA96&LPA99 cohorts. Overall, 216 patients (81%) achieved complete remission with no differences between trials. The 5-year NRM, cumulative incidence of relapse, disease-free survival and overall survival in the LPA2005 vs the LPA96&99 were 5 vs 18% (P=0.15), 7 vs 12% (P=0.23), 87 vs 69% (P=0.04) and 74 vs 60% (P=0.06). A less intensive front-line regimen with ATRA and anthracycline monochemotherapy resulted in improved outcomes in older APL patients.es
dc.language.isoenges
dc.subject.meshDisease-Free Survival *
dc.subject.meshRecurrence *
dc.subject.meshAged *
dc.subject.meshRisk Factors *
dc.subject.meshAnthracyclines *
dc.subject.meshTreatment Outcome *
dc.subject.meshRemission Induction *
dc.subject.meshLeukemia, Promyelocytic, Acute *
dc.subject.meshAntineoplastic Combined Chemotherapy Protocols *
dc.subject.meshTretinoin *
dc.titleLong-term outcome of older patients with newly diagnosed de novo acute promyelocytic leukemia treated with ATRA plus anthracycline-based therapyes
dc.typeArtigoes
dc.identifier.doi10.1038/leu.2017.178
dc.identifier.essn1476-5551
dc.identifier.pmid28584252
dc.issue.number1es
dc.journal.titleLeukemiaes
dc.organizationServizo Galego de Saúde::Áreas Sanitarias (A.S.)::Área Sanitaria de Santiago de Compostela - Complexo Hospitalario Universitario de Santiago de Compostelaes
dc.organizationServizo Galego de Saúde::Áreas Sanitarias (A.S.)::Área Sanitaria de Lugo, Cervo e Monforte de lemos - Complexo Hospitalario Universitario Lucus Augusties
dc.page.initial21es
dc.page.final29es
dc.relation.publisherversionhttps://www.nature.com/articles/leu2017178es
dc.rights.accessRightsembargoedAccesses
dc.subject.cie10Leucemia promielocítica aguda es
dc.subject.decsleucemia promielocítica aguda *
dc.subject.decsantraciclinas *
dc.subject.decsresultado del tratamiento *
dc.subject.decsprotocolos de quimioterapia antineoplásica combinada *
dc.subject.decsrecurrencia *
dc.subject.decstretinoina *
dc.subject.decsinducción de remisión *
dc.subject.decsanciano *
dc.subject.decssupervivencia sin enfermedad *
dc.subject.decsfactores de riesgo *
dc.subject.keywordATRAes
dc.subject.keywordCHUSes
dc.subject.keywordCHULAes
dc.typefidesArtigo Científico (inclue Orixinal, Orixinal breve, Revisión Sistemática e Meta-análisis)es
dc.typesophosArtículo Originales
dc.volume.number32es


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