Dexamethasone in hyperleukocytic acute myeloid leukemia
Sarah Bertoli,
Muriel Picard,
Emilie Bérard,
Emmanuel Griessinger,
Clément Larrue,
Pierre Luc Mouchel,
François Vergez,
Suzanne Tavitian,
Edwige Yon,
Jean Ruiz,
Eric Delabesse,
Isabelle Luquet,
Laetitia Karine Linares,
Estelle Saland,
Martin Carroll,
Gwenn Danet-Desnoyers,
Audrey Sarry,
Françoise Huguet,
Jean Emmanuel Sarry,
Christian Récher
Affiliations
Sarah Bertoli
Service d’Hématologie, Centre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse Oncopole, France;Université Toulouse III Paul Sabatier, France;Cancer Research Center of Toulouse, UMR1037-INSERM, ERL5294 CNRS, France
Muriel Picard
Service de Réanimation Polyvalente, Centre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse Oncopole, France
Emilie Bérard
Service d’Epidémiologie, Centre Hospitalier Universitaire de Toulouse, France;UMR 1027, INSERM-Université de Toulouse III, France
Emmanuel Griessinger
Université Côte d’Azur, INSERM U1065, Centre Méditerranéen de Médecine Moléculaire, Nice, France
Clément Larrue
Cancer Research Center of Toulouse, UMR1037-INSERM, ERL5294 CNRS, France
Pierre Luc Mouchel
Service d’Hématologie, Centre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse Oncopole, France;Cancer Research Center of Toulouse, UMR1037-INSERM, ERL5294 CNRS, France
François Vergez
Université Toulouse III Paul Sabatier, France;Cancer Research Center of Toulouse, UMR1037-INSERM, ERL5294 CNRS, France;Laboratoire d’Hématologie, Centre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse Oncopole, France
Suzanne Tavitian
Service d’Hématologie, Centre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse Oncopole, France
Edwige Yon
Service d’Epidémiologie, Centre Hospitalier Universitaire de Toulouse, France
Jean Ruiz
Service de Réanimation Polyvalente, Centre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse Oncopole, France
Eric Delabesse
Université Toulouse III Paul Sabatier, France;Cancer Research Center of Toulouse, UMR1037-INSERM, ERL5294 CNRS, France;Laboratoire d’Hématologie, Centre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse Oncopole, France
Isabelle Luquet
Laboratoire d’Hématologie, Centre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse Oncopole, France
Laetitia Karine Linares
IRCM, Institut de Recherche en Cancérologie de Montpellier-INSERM, U1194, France;Université Montpellier, F-34298, France;Institut Régional du Cancer Montpellier, France
Estelle Saland
Cancer Research Center of Toulouse, UMR1037-INSERM, ERL5294 CNRS, France
Martin Carroll
Stem Cell and Xenograft Core, University of Pennsylvania, Perelman School of Medicine, Philadelphia, PA, USA
Gwenn Danet-Desnoyers
Stem Cell and Xenograft Core, University of Pennsylvania, Perelman School of Medicine, Philadelphia, PA, USA
Audrey Sarry
Service d’Hématologie, Centre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse Oncopole, France
Françoise Huguet
Service d’Hématologie, Centre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse Oncopole, France
Jean Emmanuel Sarry
Cancer Research Center of Toulouse, UMR1037-INSERM, ERL5294 CNRS, France
Christian Récher
Service d’Hématologie, Centre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse Oncopole, France;Université Toulouse III Paul Sabatier, France;Cancer Research Center of Toulouse, UMR1037-INSERM, ERL5294 CNRS, France
Patients with acute myeloid leukemia and a high white blood cell count are at increased risk of early death and relapse. Because mediators of inflammation contribute to leukostasis and chemoresistance, dexamethasone added to chemotherapy could improve outcomes. This retrospective study evaluated the impact of adding or not adding dexamethasone to chemotherapy in a cohort of 160 patients with at least 50×109 white blood cells. In silico studies, primary samples, leukemic cell lines, and xenograft mouse models were used to explore the antileukemic activity of dexamethasone. There was no difference with respect to induction death rate, response, and infections between the 60 patients in the dexamethasone group and the 100 patients in the no dexamethasone group. Multivariate analysis showed that dexamethasone was significantly associated with improved relapse incidence (adjusted sub-HR: 0.30; 95% CI: 0.14–0.62; P=0.001), disease-free survival (adjusted HR: 0.50; 95% CI: 0.29–0.84; P=0.010), event-free survival (adjusted HR: 0.35; 95% CI: 0.21–0.58; P