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Prepublished online as a Blood First Edition Paper on March 20, 2003; DOI 10.1182/blood-2002-11-3527.

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2002-11-3527v1
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Submitted November 20, 2002
Accepted March 8, 2003

Prognosis of inv(16)/t(16;16) acute myeloid leukemia (AML): a survey of 110 cases from the French AML intergroup

Jacques Delaunay, Norbert Vey, Thierry Leblanc, Pierre Fenaux, Francoise Rigal-Huguet, Francis Witz, Thierry Lamy, Anne Auvrignon, Didier Blaise, Arnaud Pigneux, Francine Mugneret, Christian Bastard, Nicole Dastugue, Jacqueline Van den Akker, Denis Fiere, Josy Reiffers, Sylvie Castaigne, Guy Leverger, Jean-Luc Harousseau, and Herve Dombret*

Department of Hematology, Hopital Saint-Louis, Paris, France
Department of Hematology, Institut Paoli-Calmettes, Marseille, France
Department of Hematology, Hopital Claude Huriez, Lille, France
Department of Hematology, Hopital Purpan, Toulouse, France
Department of Hematology, Hopital Brabois, Nancy, France
Department of Hematology, Centre Hospitalier Pontchaillou, Rennes, France
Department of Hematology, Hopital Trousseau, Paris, France
Department of Hematology, Hopital du Haut-Leveque, Pessac, France
Department of Hematology, Hopital du Bocage, Dijon, France
Department of Hematology, Centre Henri Becquerel, Rouen, France
Department of Hematology, Hopital Saint-Antoine, Paris, France
Department of Hematology, Hopital Edouard Herriot, Lyon, France
Department of Hematology, Hopital Andre Mignot, Versailles, France
Department of Hematology, Hotel-Dieu, Nantes, France

* Corresponding author; email: herve.dombret{at}sls.ap-hop-paris.fr.

Acute myeloid leukemias carrying inv(16)/t(16;16) chromosomal abnormalities are associated with a good prognosis. However, studies of this AML subtype have been hampered by the few number of patients reported, frequently collectively considered with those with AML carrying the t(8;21) translocation. We performed a retrospective study in 110 patients with inv(16)/t(16;16) AML (median age, 34 years) prospectively enrolled in six trials conducted in France between 1987 and 1998, with the aim to investigate prognostic factors for CR achievement and outcome of CR patients in this AML subtype. CR rate was 93%. Bad-prognosis factors for CR achievement were higher WBC and lower platelet count (optimal cutpoints at 120 and 30 G/L, respectively). At 3 years, estimated overall survival, DFS, and cumulative incidence of relapse were 58%, 48%, and 42%, respectively. In multivariate analysis: 1) advanced age (optimal cutpoint, 35 years) was the only factor for shorter DFS; 2) advanced age and low platelet count were the two factors for shorter survival of CR patients. Outcome of CR patients: 1) was not influenced by WBC and cytogenetic findings; 2) was similar among patients allocated to receive allogeneic transplantation, high-dose, or intermediate-dose cytarabine. Interestingly, advanced age was associated with a trend for more frequent additional chromosome abnormalities and predictive of higher cumulative incidence of relapse rather than death in CR1. These results markedly contrast with those reported in patients with t(8;21) AML in whom WBC, and not age, was the main high-risk factor for relapse, DFS, and survival.


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