Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Original Article
  • Published:

Progenitor Cell Mobilisation

More efficient mobilisation of peripheral blood stem cells with HiDAC+AMSA+G-CSF than with mini-ICE+G-CSF in patients with AML

Summary:

We have compared the efficacy of two PBSC mobilisation regimens, mini-ICE+filgrastim (second consolidation) and HiDAC+AMSA+filgrastim (third consolidation), in two consecutive cohorts of patients with AML CR1 receiving treatment according to a joint protocol. Group A: 18 patients, aged 41 (21–65) years, were mobilised with mini-ICE (idarubicin 8 mg/m2+cytarabine 800 mg/m2+etoposide 150 mg/m2 days 1–3) followed by filgrastim 300–480 μg once daily s.c. from day 11 after start of chemotherapy. Only four patients reached >5 CD34+ cells/μl blood (B-CD34+) and were able to undergo leukaphereses. Two out of 18 (11%) reached the defined target of 2.0 × 106 CD34+ cells/kg after 1–3 leukaphereses. Group B: 20 patients, aged 50 (29–67) years, received HiDAC+AMSA (cytarabine 3 g/m2 b.i.d. days 1, 3, 5+amsacrine 150 mg/m2 q.d. days 2, 4) followed by filgrastim at a similar dose starting on day 7. A total of 18 patients reached B-CD34+ >5/μl and underwent PBSC harvesting, starting on day 23 (14–29) and yielding 4.0 (0.9–21) × 106 CD34+ cells/kg. Of 20 patients, 17 (85%) reached the defined target of 2.0 × 106 CD34+ cells/kg after 1–3 leukaphereses. We conclude that HiDAC+AMSA+G-CSF – in contrast to mini-ICE+G-CSF – is an efficient regimen for mobilising PBSC in patients with AML CR1.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Similar content being viewed by others

References

  1. Gorin NC . Autologous stem cell transplantation in acute myelocytic leukemia. Blood 1998; 92: 1073–1090.

    CAS  Google Scholar 

  2. Kimby E, Nygren P, Glimelius B . A systematic overview of chemotherapy effects in acute myeloid leukaemia. Acta Oncol 2001; 40: 231–252.

    Article  CAS  Google Scholar 

  3. Burnett A . Randomised comparison of addition of autologous bone-marrow transplantation to intensive chemotherapy for acute myeloid leukaemia in first remission: results of MRC AML 10 trial. Lancet 1998; 351: 700–708.

    Article  CAS  Google Scholar 

  4. Zittoun RA, Mandelli F, Willemze R et al. Autologous or allogeneic bone marrow transplantation compared with intensive chemotherapy in acute myelogenous leukemia. European Organization for Research and Treatment of Cancer (EORTC) and the Gruppo Italiano Malattie Ematologiche Maligne dell'Adulto (GIMEMA) Leukemia Cooperative Groups. N Engl J Med 1995; 332: 217–223.

    Article  CAS  Google Scholar 

  5. Reiffers J, Labopin M, Sanz M et al. Autologous blood cell vs marrow transplantation for acute myeloid leukemia in complete remission: an EBMT retrospective analysis. Bone Marrow Transplant 2000; 25: 1115–1119.

    Article  CAS  Google Scholar 

  6. Schmitz N, Linch D, Dreger P et al. Randomised trial of filgrastim-mobilised peripheral blood progenitor cell transplantation versus autologous bone-marrow tranplantation in lymphoma patients. Lancet 1996; 347: 353–357.

    Article  CAS  Google Scholar 

  7. Lowenberg B, van Putten WL, Ferrant A et al. Peripheral blood progenitor cell transplantation as an alternative to autologous marrow transplantation in the treatment of acute myeloid leukemia. Stem Cells 1997; 15 (Suppl 1): 177–180, discussion 81.

    Article  Google Scholar 

  8. Schlenk RF, Dohner H, Pforsich M et al. Successful collection of peripheral blood progenitor cells in patients with acute myeloid leukaemia following early consolidation therapy with granulocyte colony-stimulating factor-supported high-dose cytarabine and mitoxantrone. Br J Haematol 1997; 99: 386–393.

    Article  CAS  Google Scholar 

  9. Visani G, Lemoli R, Tosi P et al. Use of peripheral blood stem cells for autologous transplantation in acute myeloid leukemia patients allows faster engraftment and equivalent disease-free survival compared with bone marrow cells. Bone Marrow Transplant 1999; 24: 467–472.

    Article  CAS  Google Scholar 

  10. Stewart DA, Guo D, Morris D et al. Superior autologous blood stem cell mobilization from dose-intensive cyclophosphamide, etoposide, cisplatin plus G-CSF than from less intensive chemotherapy regimens. Bone Marrow Transplant 1999; 23: 111–117.

    Article  CAS  Google Scholar 

  11. Visani G, Lemoli RM, Tosi P et al. Fludarabine-containing regimens severely impair peripheral blood stem cells mobilization and collection in acute myeloid leukaemia patients. Br J Haematol 1999; 105: 775–779.

    Article  CAS  Google Scholar 

  12. Demirer T, Bensinger WI, Buckner CD . Peripheral blood stem cell mobilization for high-dose chemotherapy. J Hematother 1999; 8: 103–113.

    Article  CAS  Google Scholar 

  13. Castagnola C, Alessandrino EP, Lunghi M et al. Consolidation treatment with autologous peripheral blood progenitor cell transplantation in acute myeloid leukemia: a single center experience. Ann Hematol 2001; 80: 267–271.

    Article  CAS  Google Scholar 

  14. Carella AM, Dejana A, Lerma E et al. In vivo mobilization of karyotypically normal peripheral blood progenitor cells in high-risk MDS, secondary or therapy-related acute myelogenous leukaemia. Br J Haematol 1996; 95: 127–130.

    Article  CAS  Google Scholar 

  15. Carella AM, Lerma E, Celesti L et al. Effective mobilization of Philadelphia-chromosome-negative cells in chronic myelogenous leukaemia patients using a less intensive regimen. Br J Haematol 1998; 100: 445–448.

    Article  CAS  Google Scholar 

  16. Grimwade D, Walker H, Oliver F et al. The importance of diagnostic cytogenetics on outcome in AML: analysis of 1,612 patients entered into the MRC AML 10 trial. The Medical Research Council Adult and Children's Leukaemia Working Parties. Blood 1998; 92: 2322–2333.

    CAS  Google Scholar 

  17. Johnsen HE . Report from a Nordic workshop on CD34+ cell analysis: technical recommendations for progenitor estimation in leukapheresis from multiple myeloma patients (for the laboratories associated to the Nordic myeloma study group). J Hematother 1995; 4: 21–28.

    Article  CAS  Google Scholar 

  18. Weaver CH, Hazelton B, Birch R et al. An analysis of engraftment kinetics as a function of the CD34 content of peripheral blood progenitor cell collections in 692 patients after the administration of myeloablative chemotherapy. Blood 1995; 86: 3961–3969.

    CAS  Google Scholar 

  19. Tricot G, Jagannath S, Vesole D et al. Peripheral blood stem cell transplants for multiple myeloma: identification of favorable variables for rapid engraftment in 225 patients. Blood 1995; 85: 588–596.

    CAS  Google Scholar 

  20. Shimazaki C, Yamagata N, Tatsumi T et al. Mobilization of peripheral blood progenitor cells by high-dose Ara C, VP-16 and recombinant human granulocyte colony-stimulating factor: factors affecting progenitor cell yields. Bone Marrow Transplant 1995; 15: 763–767.

    CAS  PubMed  Google Scholar 

  21. Russell NH, McQuaker G, Stainer C et al. Stem cell mobilisation in lymphoproliferative diseases. Bone Marrow Transplant 1998; 22: 935–940.

    Article  CAS  Google Scholar 

  22. Reiffers J . Peripheral blood stem cell transplantation in acute myeloid leukemia: the experience of the Bordeaux Group. Stem Cells 1995; 13 (Suppl 3): 19–22.

    Article  Google Scholar 

  23. Ketterer N, Salles G, Moullet I et al. Factors associated with successful mobilization of peripheral blood progenitor cells in 200 patients with lymphoid malignancies. Br J Haematol 1998; 103: 235–242.

    Article  CAS  Google Scholar 

  24. Carral A, de la Rubia J, Martin G et al. Factors influencing the collection of peripheral blood stem cells in patients with acute myeloblastic leukemia and non-myeloid malignancies. Leuk Res 2003; 27: 5–12.

    Article  CAS  Google Scholar 

  25. Roberts AW, DeLuca E, Begley CG et al. Broad inter-individual variations in circulating progenitor cell numbers induced by granulocyte colony-stimulating factor therapy. Stem Cells 1995; 13: 512–516.

    Article  CAS  Google Scholar 

  26. Linker CA, Ries CA, Damon LE et al. Autologous stem cell transplantation for acute myeloid leukemia in first remission. Biol Blood Marrow Transplant 2000; 6: 50–57.

    Article  CAS  Google Scholar 

  27. Schiller G, Wong S, Lowe T et al. Transplantation of IL-2-mobilized autologous peripheral blood progenitor cells for adults with acute myelogenous leukemia in first remission. Leukemia 2001; 15: 757–763.

    Article  CAS  Google Scholar 

  28. Balduzzi A, Perseghin P, Dassi M et al. Peripheral blood stem cell collection in children with acute leukemia: effectiveness of the ‘DIAVE’ mobilizing regimen. Bone Marrow Transplant 2002; 30: 413–416.

    Article  CAS  Google Scholar 

  29. Haynes A, Hunter A, McQuaker G et al. Engraftment characteristics of peripheral blood stem cells mobilised with cyclophosphamide and the delayed addition of G-CSF. Bone Marrow Transplant 1995; 16: 359–363.

    CAS  Google Scholar 

  30. Benet I, Prosper BF, Marugan I et al. Mobilization of peripheral blood progenitor cells (PBPC) in patients undergoing chemotherapy followed by autologous peripheral blood stem cell transplant (SCT) for high risk breast cancer (HRBC). Bone Marrow Transplant 1999; 23: 1101–1107.

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to M Höglund.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Höglund, M., Brune, M., Sallerfors, B. et al. More efficient mobilisation of peripheral blood stem cells with HiDAC+AMSA+G-CSF than with mini-ICE+G-CSF in patients with AML. Bone Marrow Transplant 32, 1119–1124 (2003). https://doi.org/10.1038/sj.bmt.1704294

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/sj.bmt.1704294

Keywords

Search

Quick links