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

Treatment and long-term results in children with acute myeloid leukaemia treated according to the AIEOP AML protocols / A. Pession; R. Rondelli; G. Basso; C. Rizzari; A. M. Testi; F. Fagioli; P. De Stefano; F. Locatelli; and and on behalf of the AML Strategy & Study Committee of the Associazione Italiana di Ematologia e Oncologia Pediatrica (AIEOP). - In: LEUKEMIA. - ISSN 0887-6924. - ELETTRONICO. - 19:12(2005), pp. 2043-2053. [10.1038/sj.leu.2403869]

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

PESSION, ANDREA;
2005

Abstract

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
2005
Treatment and long-term results in children with acute myeloid leukaemia treated according to the AIEOP AML protocols / A. Pession; R. Rondelli; G. Basso; C. Rizzari; A. M. Testi; F. Fagioli; P. De Stefano; F. Locatelli; and and on behalf of the AML Strategy & Study Committee of the Associazione Italiana di Ematologia e Oncologia Pediatrica (AIEOP). - In: LEUKEMIA. - ISSN 0887-6924. - ELETTRONICO. - 19:12(2005), pp. 2043-2053. [10.1038/sj.leu.2403869]
A. Pession; R. Rondelli; G. Basso; C. Rizzari; A. M. Testi; F. Fagioli; P. De Stefano; F. Locatelli; and and on behalf of the AML Strategy & Study Committee of the Associazione Italiana di Ematologia e Oncologia Pediatrica (AIEOP)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/21800
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