After the identification of discrete relapse-risk categories in patients with acute promyelocytic leukemia (APL) receiving all-trans retinoic and idarubicin (AIDA)-like therapies, the Gruppo Italiano Malattie Ematologiche dell'Adulto (GIMEMA) designed a protocol for newly diagnosed APL (AIDA-2000) in which postremission treatment was risk-adapted. Patients with low/intermediate risk received remission at 3 anthracycline-based consolidation courses, whereas high-risk patients received the same schedule as in the previous, non-risk-adapted AIDA-0493 trial including cytarabine. In addition, all patients in the AIDA-2000 received all-trans retinoic acid (ATRA) for 15 days during each consolidation. After induction, 600 of 636 (94.3%) and 420 of 445 (94.4%) patients achieved complete remission in the AIDA-0493 and AIDA-2000, respectively. The 6-year overall survival and cumulative incidence of relapse (CIR) rates were 78.1% versus 87.4% (P = .001) and 27.7% versus 10.7% (P < .0001). Significantly lower CIR rates for patients in the AIDA-2000 were most evident in the high-risk group (49.7% vs 9.3%, respectively, P < .0001). Our data confirm that anthracycline-based consolidation is at least equally effective as cytarabine-containing regimens for low-/intermediate-risk patients and suggest that a risk-adapted strategy including ATRA for consolidation improves outcome in newly diagnosed APL. Furthermore, our results highlight the role of cytarabine coupled to anthracyclines and ATRA during consolidation in the high-risk group.

Front-line treatment of acute promyelocytic leukemia with AIDA induction followed by risk-adapted consolidation for adults younger than 61 years: results of the AIDA-2000 trial of the GIMEMA Group / Lo-Coco F.; Avvisati G.; Vignetti M.; Breccia M.; Gallo E.; Rambaldi A.; Paoloni F.; Fioritoni G.; Ferrara F.; Specchia G.; Cimino G.; Diverio D.; Borlenghi E.; Martinelli G.; Di Raimondo F.; Di Bona E.; Fazi P.; Peta A.; Bosi A.; Carella A.M.; Fabbiano F.; Pogliani E.M.; Petti M.C.; Amadori S.; Mandelli F.. - In: BLOOD. - ISSN 0006-4971. - STAMPA. - 116:17(2010), pp. 3171-3179. [10.1182/blood-2010-03-276196]

Front-line treatment of acute promyelocytic leukemia with AIDA induction followed by risk-adapted consolidation for adults younger than 61 years: results of the AIDA-2000 trial of the GIMEMA Group

MARTINELLI, GIOVANNI;
2010

Abstract

After the identification of discrete relapse-risk categories in patients with acute promyelocytic leukemia (APL) receiving all-trans retinoic and idarubicin (AIDA)-like therapies, the Gruppo Italiano Malattie Ematologiche dell'Adulto (GIMEMA) designed a protocol for newly diagnosed APL (AIDA-2000) in which postremission treatment was risk-adapted. Patients with low/intermediate risk received remission at 3 anthracycline-based consolidation courses, whereas high-risk patients received the same schedule as in the previous, non-risk-adapted AIDA-0493 trial including cytarabine. In addition, all patients in the AIDA-2000 received all-trans retinoic acid (ATRA) for 15 days during each consolidation. After induction, 600 of 636 (94.3%) and 420 of 445 (94.4%) patients achieved complete remission in the AIDA-0493 and AIDA-2000, respectively. The 6-year overall survival and cumulative incidence of relapse (CIR) rates were 78.1% versus 87.4% (P = .001) and 27.7% versus 10.7% (P < .0001). Significantly lower CIR rates for patients in the AIDA-2000 were most evident in the high-risk group (49.7% vs 9.3%, respectively, P < .0001). Our data confirm that anthracycline-based consolidation is at least equally effective as cytarabine-containing regimens for low-/intermediate-risk patients and suggest that a risk-adapted strategy including ATRA for consolidation improves outcome in newly diagnosed APL. Furthermore, our results highlight the role of cytarabine coupled to anthracyclines and ATRA during consolidation in the high-risk group.
2010
Front-line treatment of acute promyelocytic leukemia with AIDA induction followed by risk-adapted consolidation for adults younger than 61 years: results of the AIDA-2000 trial of the GIMEMA Group / Lo-Coco F.; Avvisati G.; Vignetti M.; Breccia M.; Gallo E.; Rambaldi A.; Paoloni F.; Fioritoni G.; Ferrara F.; Specchia G.; Cimino G.; Diverio D.; Borlenghi E.; Martinelli G.; Di Raimondo F.; Di Bona E.; Fazi P.; Peta A.; Bosi A.; Carella A.M.; Fabbiano F.; Pogliani E.M.; Petti M.C.; Amadori S.; Mandelli F.. - In: BLOOD. - ISSN 0006-4971. - STAMPA. - 116:17(2010), pp. 3171-3179. [10.1182/blood-2010-03-276196]
Lo-Coco F.; Avvisati G.; Vignetti M.; Breccia M.; Gallo E.; Rambaldi A.; Paoloni F.; Fioritoni G.; Ferrara F.; Specchia G.; Cimino G.; Diverio D.; Borlenghi E.; Martinelli G.; Di Raimondo F.; Di Bona E.; Fazi P.; Peta A.; Bosi A.; Carella A.M.; Fabbiano F.; Pogliani E.M.; Petti M.C.; Amadori S.; Mandelli F.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/96954
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