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Complete Remission by Imatinib Mesylate (Glivec) in a Child Relapsing with Philadelphia Chromosome Positive Acute Lymphoblastic Leukemia (Ph (+) ALL) after Unrelated Donor Stem Cell Transplantation / 대한소아혈액종양학회지
Article en Ko | WPRIM | ID: wpr-115284
Biblioteca responsable: WPRO
ABSTRACT
The prognosis of patients with Philadelphia chromosome positive acute lymphoblastic leukemia (Ph ALL) who relapsed after allogeneic stem cell transplantation (allo-SCT) is poor. Imatinib mesylate (Glivec (R) ) is an inhibitor of the ABL tyrosine kinase with potent antileukemic activity in advanced Ph ALL. The clinical effects of imatinib on Ph ALL recurring after allo-SCT have not been established. We describe the clinical activity of imatinib in a 7 year-old boy with Ph ALL relapsing after unrelated donor stem cell transplantation. Imatinib as a single agent resulted in rapid elimination of leukemic cells with ensuing prolonged neutropenia and thrombocytopenia. Subsequent hematological recovery by donor-derived cells was associated with grade 3 graft-versus-host disease (GvHD), which responded to cyclosporine A and steroid. Imatinib successfully induced hematologic, cytogenetic and molecular remission of Ph ALL, and restored complete donor chimerism, along with controllable GvHD.
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Texto completo: 1 Índice: WPRIM Asunto principal: Pronóstico / Células Madre / Trombocitopenia / Donantes de Tejidos / Proteínas Tirosina Quinasas / Cromosoma Filadelfia / Ciclosporina / Mesilatos / Citogenética / Trasplante de Células Madre Tipo de estudio: Prognostic_studies Límite: Child / Humans / Male Idioma: Ko Revista: Korean Journal of Pediatric Hematology-Oncology Año: 2003 Tipo del documento: Article
Texto completo: 1 Índice: WPRIM Asunto principal: Pronóstico / Células Madre / Trombocitopenia / Donantes de Tejidos / Proteínas Tirosina Quinasas / Cromosoma Filadelfia / Ciclosporina / Mesilatos / Citogenética / Trasplante de Células Madre Tipo de estudio: Prognostic_studies Límite: Child / Humans / Male Idioma: Ko Revista: Korean Journal of Pediatric Hematology-Oncology Año: 2003 Tipo del documento: Article