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dc.contributor.authorSteegmann, Juan Luís
dc.contributor.authorOdriozola, Jesús
dc.contributor.authorRodriguez Salvanés, Francisco
dc.contributor.authorGiraldo, Pilar
dc.contributor.authorGarcía Laraña, José
dc.contributor.authorFerro, María Teresa
dc.contributor.authorBenítez, Esmeralda
dc.contributor.authorPérez-Pons, Concepción
dc.contributor.authorGiralt, Manuel
dc.contributor.authorEscribano, Luís
dc.contributor.authorLavilla Rubira, Esperanza 
dc.contributor.authorMiguel, Amparo
dc.contributor.authorAreal Méndez, Carlos 
dc.contributor.authorPérez Encinas, Manuel Mateo 
dc.contributor.authorAbad, Ana
dc.contributor.authorMaldonado, Juan
dc.contributor.authorMassagué, Isabel
dc.contributor.authorFernández-Rañada, José María
dc.date.accessioned2026-01-27T10:38:42Z
dc.date.available2026-01-27T10:38:42Z
dc.date.issued1999
dc.identifier.issn0390-6078
dc.identifier.otherhttps://pubmed.ncbi.nlm.nih.gov/10553157/es
dc.identifier.urihttp://hdl.handle.net/20.500.11940/22541
dc.description.abstract[EN] BACKGROUND AND OBJECTIVE: Interferon-a (IFN) is increasingly being used as the drug of choice in chronic myeloid leukemia patients. The main objectives of the study were to study the influence of the classic prognostic variables and response to IFN, and to assess the influence of this response on the course of the disease and survival. DESIGN AND METHODS: Single arm, prospective, multicenter study, without a control group. Only Ph1-positive CML patients were included. The treatment scheme was biphasic: the patients first received standard chemotherapy and thereafter IFN-a2a was used as monotherapy, with a target dose of 9 MU/d/s.c. RESULTS: Twenty-one centers in Spain enrolled 132 patients (72 men, 60 women). The median dose of IFN given was 5.8 MU/d, and the median treatment duration was 431 days (range: 18-2,597). Seventy-two percent of patients obtained a hematologic response in the first six months of IFN treatment. Genetic response was obtained in 47% of the patients, and the response was major or complete in 27% and 19%, respectively. The median time to obtain this response was 7, 9, and 18 months for minimal, partial and complete genetic response, respectively. Multivariant analysis showed that only a higher percentage of basophils at diagnosis was associated with a worse hematologic response at six months (p=0.001) (OR: 1.23) and with a worse cytogenetic response in the first year of IFN therapy (p=0.018) (OR: 1.4). Over an observation period of 8 years, 35.6% of the patients died, and 85 (64.4%) remained alive. With a median follow-up of 42 months (3.7-98), the 6-year projected probabilities of survival and transformation-free survival were 0.61+/-0.07 vs. 0.54+/-0.07, respectively. Patients with Kantarjian's stage 3 disease or in a high-risk Sokal group had lower probabilities of survival, but these systems did not adequately discriminate in our series. Obtaining a complete hematologic response in the first six months of IFN therapy was favorable in terms of overall survival (p=0.05; HR=0.33). Cox's analysis demonstrated that obtaining a cytogenetic response in the first year was independently associated with better overall survival (p=0.04; HR=0.19) and better transformation-free survival (p=0.0035; HR=0.11). INTERPRETATION AND CONCLUSIONS: Nearly half of the patients obtained some degree of Philadelphia suppression, which was major in 27%, and complete in 19%. A higher percentage of basophils at diagnosis was the only variable associated with a lower probability of cytogenetic response. Obtaining a cytogenetic response during the first year of IFN treatment was a favorable and independent variable in terms of survival and transformation-free survival. Obtaining a major cytogenetic response during this period decreased the risk of transformation twenty times. Our results suggest that the effect of IFN on survival is independent of the classic prognostic variables.es
dc.language.isoenges
dc.rightsAttribution-NonCommercial 4.0 International (CC BY-NC 4.0)
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.subject.meshAged *
dc.subject.meshSpain *
dc.subject.meshInterferon alpha-2 *
dc.subject.meshCytogenetic Analysis *
dc.subject.meshPrognosis *
dc.subject.meshThrombocytopenia *
dc.subject.meshPhiladelphia Chromosome *
dc.subject.meshTime Factors *
dc.subject.meshBasophils *
dc.subject.meshTreatment Outcome *
dc.subject.meshLeukemia, Myelogenous, Chronic, BCR-ABL Positive *
dc.subject.meshInterferon-alpha *
dc.subject.meshSurvival Rate *
dc.subject.meshLeukemia, Myeloid, Chronic-Phase *
dc.titleStage, percentage of basophils at diagnosis, hematologic response within six months, cytogenetic response in the first year: the main prognostic variables affecting outcome in patients with chronic myeloid leukemia in chronic phase treated with interferon-alpha. Results of the CML89 trial of the Spanish Collaborative Group on interferon-alpha2a and CMLes
dc.typeArtigoes
dc.bbddEmbase*
dc.bbddWOK*
dc.identifier.pmid10553157
dc.issue.number11es
dc.journal.titleHaematologicaes
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.organizationServizo Galego de Saúde::Áreas Sanitarias (A.S.)::Área Sanitaria de Ferrol – Complexo Hospitalario Universitario de Ferrol::Hematoloxía clínicaes
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.page.initial978es
dc.page.final987es
dc.relation.publisherversionhttps://haematologica.org/article/view/1530es
dc.rights.accessRightsopenAccesses
dc.subject.cie10Leucemia mieloide crónica es
dc.subject.decsleucemia mielogenosa crónica BCR-ABL positiva *
dc.subject.decsleucemia mieloide de fase crónica *
dc.subject.decscromosoma Filadelfia *
dc.subject.decsfactores de tiempo *
dc.subject.decsanciano *
dc.subject.decstasa de supervivencia *
dc.subject.decspronóstico *
dc.subject.decsbasófilos *
dc.subject.decsresultado del tratamiento *
dc.subject.decsanálisis citogenético *
dc.subject.decsInterferón alfa-2 *
dc.subject.decsinterferón alfa *
dc.subject.decstrombocitopenia *
dc.subject.keywordCHULAes
dc.subject.keywordCHUFes
dc.subject.keywordCHUSes
dc.typefidesArtigo Científico (inclue Orixinal, Orixinal breve, Revisión Sistemática e Meta-análisis)es
dc.typesophosArtículo Originales
dc.volume.number84es


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