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1.
Yonsei Medical Journal ; : 91-96, 1994.
Artículo en Inglés | WPRIM | ID: wpr-171806

RESUMEN

We describe a case with acute myelogenous leukemia (AML; M2) who developed prolonged marrow hypoplasia with residual leukemic blasts and recurrent infections after induction chemotherapy. He was treated successfully with a sequential treatment of recombinant human granulocyte-macrophage colony-stimulating factor (rhGM-CSF) and low-dose cytosine arabinoside (LD AraC). To the best of our knowledge this is the first reported case of a successful treatment of a patient with AML, who showed prolonged markedly hypocellular bone marrow with significant residual leukemic cells after induction chemotherapy, with a sequential treatment of GM-CSF and LD AraC.


Asunto(s)
Humanos , Masculino , Enfermedades de la Médula Ósea/inducido químicamente , Citarabina/administración & dosificación , Factor Estimulante de Colonias de Granulocitos y Macrófagos/uso terapéutico , Leucemia Mieloide Aguda/tratamiento farmacológico , Persona de Mediana Edad
2.
Journal of the Korean Pediatric Society ; : 9-16, 1993.
Artículo en Coreano | WPRIM | ID: wpr-122996

RESUMEN

We analyzed the clinical and laboratory features of ten children with acute megakaryoblastic lukemia (M7)and compared the findings with those reported in the literature. The diagnosis was supprted by ultrastructural examination of platelet peroxidase or immunophenotyping for glycoprotein IIb/IIIa. Of the ten children, five were girls and five were boys. The median age at diagnosis was 13 months. Two patients had prominent myelofibrosis and one patient had Down syndrome. Nine patients were treatd with low-dose cytosine arabinoside (10mg/m2)administered intravenously, or subcutaneously, or intramuscularly, twice daily in 21 day courses. Seven patients achieved hematologic response and three patients are alive without evidence of disease. The 4 year event free survival rate was30.0%. It is our impression that the prevalence of acute megakaryoblastic leukemia has been under-estimated, and low-dose cytosine arabinoside treatment may be of value in its management. This approach may be particularily useful in hospitals with scarce well-equipped facilities, since this protocol does not induce profound marrow hypoplasia and intensive supportive measures are not required as they would be with the use of more aggressive drug combination.


Asunto(s)
Niño , Femenino , Humanos , Plaquetas , Médula Ósea , Citarabina , Diagnóstico , Supervivencia sin Enfermedad , Síndrome de Down , Glicoproteínas , Inmunofenotipificación , Leucemia Megacarioblástica Aguda , Células Progenitoras de Megacariocitos , Peroxidasa , Prevalencia , Mielofibrosis Primaria
3.
Journal of Kunming Medical University ; (12)1988.
Artículo en Chino | WPRIM | ID: wpr-673137

RESUMEN

In this paper, acute nonlyumphocytic leukemia that is not fit for strong chemotherapy treated with low dose cytosine arabinoside (Ara—c) in 11 cases is presented. One of the patients got a complete remission and another was partial remiss, the total remission rate being 18.2%. The therapeutic mechanism, side effect, and remission rate of low dose Ara-c have been discussed. The authors conclude that this treatment is still of choice to the patients who are not fit for strong chemotherapy.

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