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A randomized study of intermediate as compared with high doses of interferon-alpha for chronic myeloid leukemia: no differences in cytogenetic responses

Penarrubia, M. J.; Odriozola, J.; González, C.; Massagué, I.; Miguel, A.; González San Miguel, J. D.; Pérez Encinas, Manuel Mateo; Lavilla Rubira, Esperanza; Giraldo, M. P.; Casado, L. F.; Ferrer, S.; Steegmann, J. L.
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URI: http://hdl.handle.net/20.500.11940/22522
PMID: 14517691
DOI: 10.1007/s00277-003-0724-z
ESSN: 1432-0584
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Ann Hematol. 2003 Dec;82(12):750-8 (193.8Kb)
VERSIÓN DEL EDITOR (62.77Kb)
Date issued
2003
Journal title
Annals of Hematology
Type of content
Artigo
DeCS
leucemia mielogenosa crónica BCR-ABL positiva | análisis de supervivencia | análisis citogenético | humanos | antineoplásicos | relación dosis-respuesta de medicamentos | interferón alfa | estudios de seguimiento | ensayo clínico
MeSH
Dose-Response Relationship, Drug | Spain | Follow-Up Studies | Humans | Leukemia, Myelogenous, Chronic, BCR-ABL Positive | Interferon-alpha | Cytogenetic Analysis | Survival Analysis | Clinical Trial | Antineoplastic Agents
CIE
Leucemia mieloide crónica
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.

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