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Maintenance Therapy With Interleukin-2 for Childhood AML: Results of ELAM02 Phase III Randomized Trial.
Petit, Arnaud; Ducassou, Stéphane; Leblanc, Thierry; Pasquet, Marlène; Rousseau, Alexandra; Ragu, Christine; Cachanado, Marine; Nelken, Brigitte; Bertrand, Yves; Michel, Gérard; Gandemer, Virginie; Cuccuini, Wendy; Fenneteau, Odile; Lapillonne, Hélène; Auvrignon, Anne; Baruchel, André; Leverger, Guy.
Afiliação
  • Petit A; Department of Pediatric Hematology and Oncology, Assistance Publique-Hôpitaux de Paris, GH HUEP, Armand Trousseau Hospital, Paris, France; Sorbonne Université, UMRS_938, Paris, France.
  • Ducassou S; Department of Pediatric Hematology and Oncology, Children's Hospital, Bordeaux University, Bordeaux, France.
  • Leblanc T; Department of Pediatric Hematology and Immunology, Robert Debré Hospital, AP-HP and University Paris Diderot, Paris, France.
  • Pasquet M; Department of Pediatric Hematology, Children's Hospital and CRCT-Oncopole, Toulouse, France.
  • Rousseau A; Department of Clinical Pharmacology and Unité de Recherche Clinique, AP-HP, Hôpital Saint Antoine, Paris, France; Sorbonne Université, Paris, France.
  • Ragu C; Department of Pediatric Hematology and Oncology, Assistance Publique-Hôpitaux de Paris, GH HUEP, Armand Trousseau Hospital, Paris, France; Sorbonne Université, UMRS_938, Paris, France.
  • Cachanado M; Department of Clinical Pharmacology and Unité de Recherche Clinique, AP-HP, Hôpital Saint Antoine, Paris, France; Sorbonne Université, Paris, France.
  • Nelken B; Department of Pediatric Hematology-Oncology, Jeanne de Flandre Hospital, CHRU and Lille 2 University, Lille, France.
  • Bertrand Y; Department of Immuno-Hemato-Pediatrics, Hospices Civils de Lyon, Claude Bernard University, Lyons, France.
  • Michel G; Department of Pediatric Hematology and Oncology and Research Unit EA 3279, Aix-Marseille University and Timone Hospital, Marseilles, France.
  • Gandemer V; Department of Pediatric Hematology and Oncology, University Hospital of Rennes, Rennes, France.
  • Cuccuini W; Department of Cytogenetics, Saint-Louis Hospital, AP-HP, Paris, France.
  • Fenneteau O; Laboratory of Hematology, Robert Debré Hospital, AP-HP, Paris, France; University Paris Diderot, Paris, France.
  • Lapillonne H; Laboratory of Hematology, Armand Trousseau Hospital, AP-HP and Sorbonne Université, UMRS_938, Paris, France.
  • Auvrignon A; Department of Pediatric Hematology and Oncology, Assistance Publique-Hôpitaux de Paris, GH HUEP, Armand Trousseau Hospital, Paris, France; Sorbonne Université, UMRS_938, Paris, France.
  • Baruchel A; Department of Pediatric Hematology and Immunology, Robert Debré Hospital, AP-HP and University Paris Diderot, Paris, France.
  • Leverger G; Department of Pediatric Hematology and Oncology, Assistance Publique-Hôpitaux de Paris, GH HUEP, Armand Trousseau Hospital, Paris, France; Sorbonne Université, UMRS_938, Paris, France.
Hemasphere ; 2(6): e159, 2018 Dec.
Article em En | MEDLINE | ID: mdl-31723797
ABSTRACT
Despite significant progress in the treatment of pediatric acute myeloblastic leukemia (AML), relapse remains the commonest cause of death. Randomized ELAM02 trial questioned if maintenance therapy with interleukin-2 (IL2), for 1 year, improves disease-free survival (DFS). Patients aged 0 to 18 years, with newly diagnosed AML (excluding patients with acute promyelocytic leukemia or down syndrome AML) were enrolled. They received 1 course of induction treatment (cytarabine and mitoxantrone) and 3 courses of consolidation treatment (high-dose cytarabine in courses 1 and 3). According to the cytogenetics risk, patients not undergoing hematopoietic stem cell transplantation, still in complete remission (CR) after the third course of consolidation treatment, were eligible for randomization to 1 year of maintenance therapy with monthly courses of IL2 or no maintenance treatment. There were 438 evaluable patients, 154 of whom were randomized to the IL2/no maintenance groups. Relapse occurred in 28 patients from the IL2+ group and 29 patients in the IL2- group. Survival was similar in the 2 groups, with a 4-year DFS of 62% without IL2 and 66% with IL2 (P = 0.75). In the CBF population, 4-year DFS was 55% without IL2 and 78% with IL2 (P = 0.07). No deaths from toxicity or excess of serious adverse events related to IL2 treatment were recorded. Prolonged IL2 for maintenance therapy after intensive chemotherapy is feasible and safe in pediatric AML patients in their first CR. Such treatment did not improve DFS in this study, but a positive trend was observed in favor of IL2 maintenance therapy among core binding factor acute myeloblastic leukemia.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials Idioma: En Revista: Hemasphere Ano de publicação: 2018 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials Idioma: En Revista: Hemasphere Ano de publicação: 2018 Tipo de documento: Article País de afiliação: França