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Clofarabine with high dose cytarabine and granulocyte colony-stimulating factor (G-CSF) priming for relapsed and refractory acute myeloid leukaemia

  • Pamela S. Becker
  • , Hagop M. Kantarjian
  • , Frederick R. Appelbaum
  • , Stephen H. Petersdorf
  • , Barry Storer
  • , Sherry Pierce
  • , Jianqin Shan
  • , Paul C. Hendrie
  • , John M. Pagel
  • , Andrei R. Shustov
  • , Derek L. Stirewalt
  • , Stephan Faderl
  • , Elizabeth Harrington
  • , Elihu H. Estey

    Research output: Contribution to journalArticlepeer-review

    78 Scopus citations

    Abstract

    This phase I/II study was conducted to determine the maximum tolerated dose, toxicity, and efficacy of clofarabine in combination with high dose cytarabine and granulocyte colony-stimulating factor (G-CSF) priming (GCLAC), in the treatment of patients with relapsed or refractory acute myeloid leukaemia (AML). Dose escalation of clofarabine occurred without dose-limiting toxicity, so most patients were treated at the maximum dose, 25mg/m 2 per day with cytarabine 2g/m 2 per day, each for 5d, and G-CSF 5μg/kg, beginning the day before chemotherapy and continuing daily until neutrophil recovery. The complete remission (CR) rate among the 46 evaluable patients was 46% (95% confidence interval [CI] 31-61%) and the CR+CR but with a platelet count <100×10 9/l ratewas 61% (95% CI 45-75%). Multivariate analysis showed that responses to GCLAC were independent of age, cytogenetic risk category, and number of prior salvage regimens. GCLAC is highly active in relapsed and refractory AML and warrants prospective comparison to other regimens, as well as study in untreated patients.

    Original languageEnglish
    Pages (from-to)182-189
    Number of pages8
    JournalBritish Journal of Haematology
    Volume155
    Issue number2
    DOIs
    StatePublished - Oct 2011

    Keywords

    • Clinical trial phase 1
    • Clinical trial phase 2
    • Multivariate analysis
    • Remission induction
    • Salvage therapy

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