Mostrar el registro sencillo del ítem

dc.contributor.authorPenarrubia, M. J.
dc.contributor.authorOdriozola, J.
dc.contributor.authorGonzález, C.
dc.contributor.authorMassagué, I.
dc.contributor.authorMiguel, A.
dc.contributor.authorGonzález San Miguel, J. D.
dc.contributor.authorPérez Encinas, Manuel Mateo 
dc.contributor.authorLavilla Rubira, Esperanza 
dc.contributor.authorGiraldo, M. P.
dc.contributor.authorCasado, L. F.
dc.contributor.authorFerrer, S.
dc.contributor.authorSteegmann, J. L.
dc.date.accessioned2026-01-26T12:15:24Z
dc.date.available2026-01-26T12:15:24Z
dc.date.issued2003
dc.identifier.otherhttps://pubmed.ncbi.nlm.nih.gov/14517691/es
dc.identifier.urihttp://hdl.handle.net/20.500.11940/22522
dc.description.abstract[EN] Interferon-alpha (IFN-alpha) is a therapy of unquestionable efficacy in chronic myeloid leukemia (CML) patients. The best dose of IFN-alpha in the treatment of CML still remains controversial. Our primary objective was to compare cytogenetic responses in patients treated with intermediate versus high doses of IFN-alpha. A multicenter randomized controlled trial was conducted involving 109 patients with untreated CML in chronic phase from 26 Spanish hospitals. Patients were assigned to receive either an intermediate (2.5 MU/m(2) per day) or high (5 MU/m(2) per day) target dose of IFN-alpha. Hydroxyurea was allowed in both groups. In total, 108 patients were analyzed, 53 in the intermediate- and 55 in the high-dose group. Median follow-up was 47.5 months. The dose of IFN-alpha actually given was lower in the intermediate-dose group (3.83 MU/day) than in the high-dose group (6.6 MU/day) ( p<0.001). The rate of complete cytogenetic response was 24.5% in the intermediate- and 12.7% in the high-dose group (NS). A partial cytogenetic response was obtained in 7.5% and 10.9%, respectively. Cox analysis did not reveal any influence of the randomization arm on cytogenetic response rate. Ten patients in each group discontinued IFN-alpha because of toxicity. Albeit not our primary objective, no differences were found in terms of survival or transformation rate between both groups. Median survival was 73 months; 64% of patients remained free of transformation at 5 years. In terms of cytogenetic response, intermediate doses of IFN-alpha are as effective as high doses in the treatment of CML.es
dc.language.isoenges
dc.subject.meshDose-Response Relationship, Drug *
dc.subject.meshSpain *
dc.subject.meshFollow-Up Studies *
dc.subject.meshHumans *
dc.subject.meshLeukemia, Myelogenous, Chronic, BCR-ABL Positive *
dc.subject.meshInterferon-alpha *
dc.subject.meshCytogenetic Analysis *
dc.subject.meshSurvival Analysis *
dc.subject.meshClinical Trial *
dc.subject.meshAntineoplastic Agents *
dc.titleA randomized study of intermediate as compared with high doses of interferon-alpha for chronic myeloid leukemia: no differences in cytogenetic responseses
dc.typeArtigoes
dc.identifier.doi10.1007/s00277-003-0724-z
dc.identifier.essn1432-0584
dc.identifier.pmid14517691
dc.issue.number12es
dc.journal.titleAnnals of Hematologyes
dc.organizationServizo Galego de Saúde::Áreas Sanitarias (A.S.)::Área Sanitaria de Santiago de Compostela - Complexo Hospitalario Universitario de Santiago de Compostela::Hematoloxía clínicaes
dc.organizationServizo Galego de Saúde::Áreas Sanitarias (A.S.)::Área Sanitaria de Lugo, Cervo e Monforte de lemos - Complexo Hospitalario Universitario Lucus Augusti::Hematoloxía clínicaes
dc.page.initial750es
dc.page.final758es
dc.relation.publisherversionhttps://link.springer.com/article/10.1007/s00277-003-0724-zes
dc.rights.accessRightsembargoedAccesses
dc.subject.cie10Leucemia mieloide crónica es
dc.subject.decsleucemia mielogenosa crónica BCR-ABL positiva *
dc.subject.decsanálisis de supervivencia *
dc.subject.decsanálisis citogenético *
dc.subject.decshumanos *
dc.subject.decsantineoplásicos *
dc.subject.decsrelación dosis-respuesta de medicamentos *
dc.subject.decsinterferón alfa *
dc.subject.decsestudios de seguimiento *
dc.subject.decsensayo clínico *
dc.subject.keywordCHUSes
dc.subject.keywordCHULAes
dc.typefidesArtigo Científico (inclue Orixinal, Orixinal breve, Revisión Sistemática e Meta-análisis)es
dc.typesophosArtículo Originales
dc.volume.number82es


Ficheros en el ítem

Este ítem aparece en la(s) siguiente(s) colección(ones)

Mostrar el registro sencillo del ítem