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Cytogenetics and outcome of allogeneic transplantation in first remission of acute myeloid leukemia: the French pediatric experience.
Alloin, A-L; Leverger, G; Dalle, J-H; Galambrun, C; Bertrand, Y; Baruchel, A; Auvrignon, A; Gandemer, V; Ragu, C; Loundou, A; Bilhou-Nabera, C; Lafage-Pochitaloff, M; Dastugue, N; Nelken, B; Jubert, C; Rialland, F; Plat, G; Pochon, C; Vannier, J-P; Rohrlich, P-S; Kanold, J; Lutz, P; Sirvent, A; Oudin, C; Cuccuini, W; Michel, G.
Affiliation
  • Alloin AL; Department of Pediatric Hematology and Oncology, Timone Enfants Hospital and Aix-Marseille University, Marseille, France.
  • Leverger G; Department of Pediatric Hematology and Oncology, AP-HP, GH HUEP, Trousseau Hospital, Paris, France.
  • Dalle JH; UPMC University Paris 6, Paris, France.
  • Galambrun C; Department of Pediatric Hematology and Oncology, Robert Debré Hospital, Paris, France.
  • Bertrand Y; Department of Pediatric Hematology and Oncology, Timone Enfants Hospital and Aix-Marseille University, Marseille, France.
  • Baruchel A; Department of Pediatric Hematology and Oncology, University Hospital of Lyon, Lyon, France.
  • Auvrignon A; Department of Pediatric Hematology and Oncology, Robert Debré Hospital, Paris, France.
  • Gandemer V; Department of Pediatric Hematology and Oncology, AP-HP, GH HUEP, Trousseau Hospital, Paris, France.
  • Ragu C; Department of Pediatric Hematology and Oncology, University Hospital of Rennes, Rennes, France.
  • Loundou A; Department of Pediatric Hematology and Oncology, AP-HP, GH HUEP, Trousseau Hospital, Paris, France.
  • Bilhou-Nabera C; Research Unit EA3279 and Department of Public Health, Aix-Marseille University and Timone Hospital Marseille, Marseille, France.
  • Lafage-Pochitaloff M; Department of Genetics, St Antoine Hospital, Paris, France.
  • Dastugue N; Department of Genetics, Timone Enfants Hospital and Aix-Marseille University, Marseille, France.
  • Nelken B; Department of Genetics, University hospital of Toulouse, Toulouse, France.
  • Jubert C; CHU Lille, Department of Pediatric Hematology and Oncology, Lille, France.
  • Rialland F; Department of Pediatric Hematology and Oncology, University Hospital of Bordeaux, Bordeaux, France.
  • Plat G; Department of Pediatric Hematology and Oncology, University Hospital of Nantes, Nantes, France.
  • Pochon C; Department of Pediatric Hematology and Oncology, University Hospital of Toulouse, Toulouse, France.
  • Vannier JP; Department of Pediatric Hematology and Oncology, Hôpital d'Enfants de Brabois, Vandoeuvre Les Nancy, France.
  • Rohrlich PS; Department of Pediatric Hematology and Oncology, University Hospital of Rouen, Rouen, France.
  • Kanold J; Department of Pediatric Hematology and Oncology, University Hospital L'Archet, Nice, France.
  • Lutz P; Department of Pediatric Hematology and Oncology, CIC Inserm 501, University Hospital of Clermont-Ferrand, Clermont-Ferrand, France.
  • Sirvent A; Department of Pediatric Hematology and Oncology, Hospital University, Strasbourg, France.
  • Oudin C; Department of Pediatric Hematology and Oncology, University Hospital, Montpellier, France.
  • Cuccuini W; Department of Pediatric Hematology and Oncology, Timone Enfants Hospital and Aix-Marseille University, Marseille, France.
  • Michel G; Research Unit EA3279 and Department of Public Health, Aix-Marseille University and Timone Hospital Marseille, Marseille, France.
Bone Marrow Transplant ; 52(4): 516-521, 2017 Apr.
Article in En | MEDLINE | ID: mdl-27941778
ABSTRACT
We analyzed the impact of cytogenetics on 193 children enrolled in two successive French trials (LAME89/91 and ELAM02), who received hematopoietic stem cell transplantation during CR1. Detailed karyotype was available for 66/74 (89%) in LAME89/91 and 118/119 (99%) in ELAM02. Several karyotype and transplant characteristics differed according to therapeutic protocol unfavorable karyotypes were more frequent in ELAM02 (36% vs 18%), pretransplant chemotherapy included high-dose cytarabine in ELAM02 and not in LAME89/91, IV replaced oral busulfan in the conditioning regimen, methotrexate was removed from post-transplant immunosuppression, and matched unrelated donor and cord blood transplantation were introduced. Five-year overall survival (OS) was 78.2% in LAME89 and 81.4% in ELAM02. OS was significantly lower for the unfavorable cytogenetic risk group in LAME89/91 when compared with intermediate and favorable groups (50% vs 90.6 and 86.4%, P=0.001). This difference was no longer apparent in ELAM02 (80.9% vs 71.3% and 5/5, respectively). Survival improvement for children with unfavorable karyotype was statistically significant (P=0.026) and was due to decrease in relapse risk. Five-year transplantation-related mortality was 6.75% in LAME89/91. In ELAM02, it was 3.2% for patients with a sibling donor and 10.9% with an unrelated donor or cord blood. We conclude that the outcome of children with unfavorable karyotype transplanted in CR1 has improved.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Leukemia, Myeloid, Acute / Hematopoietic Stem Cell Transplantation / Cytogenetics Type of study: Guideline Limits: Child / Female / Humans / Male Country/Region as subject: Europa Language: En Journal: Bone Marrow Transplant Journal subject: TRANSPLANTE Year: 2017 Type: Article Affiliation country: France

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Leukemia, Myeloid, Acute / Hematopoietic Stem Cell Transplantation / Cytogenetics Type of study: Guideline Limits: Child / Female / Humans / Male Country/Region as subject: Europa Language: En Journal: Bone Marrow Transplant Journal subject: TRANSPLANTE Year: 2017 Type: Article Affiliation country: France