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Treatment and long-term results in children with acute myeloid leukaemia treated according to the AIEOP AML protocols
Treatment and long-term results in children with acute myeloid leukaemia treated according to the AIEOP AML protocols
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Treatment and long-term results in children with acute myeloid leukaemia treated according to the AIEOP AML protocols
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Treatment and long-term results in children with acute myeloid leukaemia treated according to the AIEOP AML protocols
Treatment and long-term results in children with acute myeloid leukaemia treated according to the AIEOP AML protocols

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Treatment and long-term results in children with acute myeloid leukaemia treated according to the AIEOP AML protocols
Treatment and long-term results in children with acute myeloid leukaemia treated according to the AIEOP AML protocols
Journal Article

Treatment and long-term results in children with acute myeloid leukaemia treated according to the AIEOP AML protocols

2005
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Overview
Since 1982, four consecutive studies on childhood acute myeloid leukaemia (AML) (namely LAM-82, -87, -87M and -92) have been conducted in Italy by the Associazione Italiana di Ematologia e Oncologia Pediatrica (AIEOP) group. The induction therapy of the first three studies consisted of daunorubicin and cytarabine structured in a 3+7 backbone. In the most recent protocol (LAM92), patients received two induction courses including idarubicin, cytarabine and etoposide. Patients with acute promyelocytic leukaemia (20% of diagnoses) were included in LAM-87 and 87M studies. Postremissional therapy significantly changed over time, with an ever-increasing role given to stem cell transplantation (SCT). The long-term outcome of patients enrolled in the LAM-82, 87 and 87M studies was comparable, whereas that of children treated according to LAM-92 study was significantly better ( P <0.005). Either allogeneic or autologous SCT was employed as consolidation therapy in more than 75% of cases enrolled in this latter study. Patients enrolled in the LAM-92 study were stratified in standard and high-risk groups with different outcome (67 vs 47%, respectively, P =0.04). Altogether, the results obtained in these four studies have permitted a progressive refinement of treatment, contributing to the structure of the ongoing LAM-2002 protocol that stratifies patients according to the presence of definite genetic anomalies and response to induction therapy.