Journal of Cancer Research and Clinical Oncology

, Volume 140, Issue 8, pp 1391–1397

Efficacy and feasibility of cyclophosphamide combined with intermediate- dose or high-dose cytarabine for relapsed and refractory acute myeloid leukemia (AML)

  • Ulf Schnetzke
  • Peter Fix
  • Baerbel Spies-Weisshart
  • Karin Schrenk
  • Anita Glaser
  • Hans-Joerg Fricke
  • Paul La Rosée
  • Andreas Hochhaus
  • Sebastian Scholl
Original Article – Clinical Oncology

DOI: 10.1007/s00432-014-1666-7

Cite this article as:
Schnetzke, U., Fix, P., Spies-Weisshart, B. et al. J Cancer Res Clin Oncol (2014) 140: 1391. doi:10.1007/s00432-014-1666-7

Abstract

Background

Approximately, 70 % of adult patients with de novo acute myeloid leukemia (AML) achieve a complete remission (CR) while 10–20 % of AML are refractory to induction chemotherapy. Furthermore, a significant proportion of AML patients in CR will relapse during or after consolidation treatment. There is no evidence for a standard salvage regimen and most centers use a combination of an anthracycline and cytarabine (AraC). The aim of this study was to investigate the impact of two age-adjusted regimens containing AraC and cyclophosphamide applied for the treatment of relapsed or refractory AML.

Patients and methods

We retrospectively analyzed 60 patients (24 male, 36 female; median age 56 years) with relapsed or refractory AML who were treated with a combination of AraC and cyclophosphamide monocentrically between October 2000 and January 2013. Two different protocols containing either high-dose (hAC) or intermediate-dose cytarabin (iAC) have been applied dependent on age and performance status.

Results

We demonstrate an overall response rate (CR + PR) induced by hAC and iAC of 56.7 %. Importantly, a complete remission rate (CR + CRp) of 52.2 % was found in patients who received the hAC regimen while only 8.8 % of patients achieved a CR following the iAC protocol (p < 0.001). The rate of refractory disease was 26.1 and 47.1 %, respectively. High-risk cytogenetics, i.e., a complex aberrant or monosomal karyotype had no effect on achievement of CR after hAC. In addition, there was no impact of activating FLT3 mutations on response to treatment according to the hAC regimen. In the cohort of patients treated with the iAC protocol, treatment-related mortality of 11.8 % within 60 days was observed but none of the patients who received the hAC regimen died within the first 2 months following chemotherapy. The toxicity profile was acceptable at both cytarabine dose levels. Importantly, 19 patients (82.6 %) of the hAC cohort underwent allogeneic hematopoietic stem cell transplantation (HSCT) as consecutive treatment.

Conclusion

The hAC regimen represents a promising therapeutic approach to induce a second CR in younger patients with relapsed or refractory AML prior to HSCT without using anthracyclines.

Keywords

AMLRelapseFLT3CyclophosphamideStem cell transplantation

Copyright information

© Springer-Verlag Berlin Heidelberg 2014

Authors and Affiliations

  • Ulf Schnetzke
    • 1
  • Peter Fix
    • 3
  • Baerbel Spies-Weisshart
    • 1
  • Karin Schrenk
    • 1
  • Anita Glaser
    • 2
  • Hans-Joerg Fricke
    • 1
  • Paul La Rosée
    • 1
  • Andreas Hochhaus
    • 1
  • Sebastian Scholl
    • 1
  1. 1.Abteilung Hämatologie und Internistische Onkologie, Klinik für Innere Medizin IIUniversitätsklinikum JenaJenaGermany
  2. 2.Institut für HumangenetikUniversitätsklinikum JenaJenaGermany
  3. 3.Abteilung Internistische Onkologie und HämatologieZentralklinik Bad BerkaBad BerkaGermany