French “real life-experience of clofarabine in children with refractory or relapsed acute lymphoblastic leukaemia
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  • 作者:Pascale Trioche (1)
    Brigitte Nelken (2)
    Gérard Michel (3)
    Isabelle Pellier (4)
    Arnaud Petit (5)
    Yves Bertrand (6)
    Pierre Rohrlich (7)
    Claudine Schmitt (8)
    Nicolas Sirvent (9)
    Patrick Boutard (10)
    Geneviève Margueritte (11)
    Brigitte Pautard (12)
    Stéphane Ducassou (13)
    Dominique Plantaz (14)
    Alain Robert (15)
    Caroline Thomas (16)
    Kristell Desseaux (17)
    Sylvie Chevret (17)
    André Baruchel (18)
  • 关键词:Acute lymphoblastic leukaemia ; Childhood leukaemia ; Refractory ; Relapsed ; Leukaemia ; Clofarabine
  • 刊名:Experimental Hematology & Oncology
  • 出版年:2012
  • 出版时间:December 2012
  • 年:2012
  • 卷:1
  • 期:1
  • 全文大小:292KB
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  • 作者单位:Pascale Trioche (1)
    Brigitte Nelken (2)
    Gérard Michel (3)
    Isabelle Pellier (4)
    Arnaud Petit (5)
    Yves Bertrand (6)
    Pierre Rohrlich (7)
    Claudine Schmitt (8)
    Nicolas Sirvent (9)
    Patrick Boutard (10)
    Geneviève Margueritte (11)
    Brigitte Pautard (12)
    Stéphane Ducassou (13)
    Dominique Plantaz (14)
    Alain Robert (15)
    Caroline Thomas (16)
    Kristell Desseaux (17)
    Sylvie Chevret (17)
    André Baruchel (18)

    1. Department of Pediatric, APHP, H?pital Antoine Béclère, Service de Pédiatrie, 157 rue de la porte de Trivaux, 92141, Clamart Cedex, France
    2. CHU, Lille, France
    3. H?pital La Timone, APHM, Marseille, France
    4. CHU, Angers, France
    5. APHP, H?pital Armand Trousseau, Paris, France
    6. CHU, Lyon, France
    7. CHU, Besan?on, France
    8. CHU, Nancy, France
    9. CHU, Nice, France
    10. CHU, Caen, France
    11. CHU, Montpellier, France
    12. CHU, Amiens, France
    13. CHU, Bordeaux, France
    14. CHU, Grenoble, France
    15. CHU, Toulouse, France
    16. CHU, Nantes, France
    17. APHP, H?pital Saint-Louis, Département de Biostatistique et Informatique Médicale, Paris et Université Paris Diderot, Paris, France
    18. APHP, H?pital Robert Debré, Hématologie et Immunologie Pédiatrique, Paris, et Université Paris Diderot, Paris, France
  • ISSN:2162-3619
文摘
Background Clofarabine alone or in combination with cyclophosphamide and etoposide has shown a good efficacy and a tolerable toxicity profile in previous studies of children with relapsed or refractory leukaemia. This report describes a retrospective study of 38 French patients who received clofarabine as a monotherapy or in combination for relapsed or refractory acute lymphoblastic leukaemia (ALL) outside of clinical trials after marketing authorization. Methods We retrospectively analysed data for 38 patients, up to 21 years old, attending 17 French centres. Thirty patients received clofarabine alone or in combination for a bone marrow relapse of acute lymphoblastic leukaemia (ALL) or refractory disease and eight patients for a high level of minimal residual disease (MRD). Survival and response durations were estimated by the Kaplan-Meier method. Results For the 30 patients who received clofarabine for a bone marrow relapse of ALL (number of relapse, 1-3; median, 1), the overall remission rate (ORR) was 37%: eight complete remission (CR) and three complete remission without platelet recovery (CRp). Ten of the 11 responding patients subsequently underwent haematopoietic stem cell transplantation (HSCT). Only four of the eight patients who received clofarabine while in remission for a high level of MRD, showed a moderate improvement of MRD. Seven of these eight patients received HSCT and six of them were alive at the end of the study. One other patient was alive without receiving HSCT. However, clofarabine treatment was associated with a high risk of infection and hepatotoxicity. Febrile neutropenia grade ?3 was reported in 79% of patients and documented infections grade ?3 occurred in nine patients (24%). Hepatotoxicity grade 3 was reported in nine patients (24%). We observed four deaths related to treatment. Conclusion In our experience, the efficacy of clofarabine is poorer than previously reported. Its toxicity is high and can be life threatening. Prospective studies on clofarabine used during earlier phases of the disease may help to define how best this new drug can be exploited for childhood and adolescent ALL.

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