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:

Autografting

Autologous transplantation for primary systemic AL amyloidosis is feasible outside a major amyloidosis referral centre: the Calgary BMT Program experience

Summary:

Recent reports from large amyloidosis referral centers suggest that primary systemic AL amyloidosis patients treated with high-dose melphalan (HDM) and autologous stem cell transplantation (ASCT) survive longer than historical controls treated with less intensive chemotherapy, despite high transplant-related mortality (TRM) rates of >10%. A retrospective review was conducted to determine if the outcome of ASCT for AL amyloidosis at our institution was similar to that reported at major amyloidosis referral centers. Over a 7 year period, we treated a total of 15 AL amyloidosis patients with ASCT, including four with poor prognosis cardiac or multisystem involvement. No TRM was observed. Overall, 10 patients (67%) achieved a complete hematological response and four patients (27%) achieved a complete organ response. The 4-year event-free and overall survival rates were 60% (95% CI 32–89%) and 75% (95% CI 50–100%), respectively. One patient, who presented with cardiac failure and multiorgan involvement with colonic bleeding currently remains in complete remission 62 months post-ASCT. In conclusion, ASCT for primary AL amyloidosis can safely be performed at experienced transplant centers that are not associated with major amyloidosis referral centers, and is feasible for patients who have multisystem involvement, particularly for motivated patients with good performance status.

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

Figure 1

Similar content being viewed by others

References

  1. Kyle RA, Bayrd ED . Amyloidosis: review of 236 cases. Medicine (Baltimore) 1975; 54: 271–299.

    Article  CAS  Google Scholar 

  2. Dubrey SW, Cha K, Anderson J et al. The clinical features of immunoglobulin light-chain (AL) amyloidosis with heart involvement. QJM 1998; 91: 141–157.

    Article  CAS  PubMed  Google Scholar 

  3. Kyle RA, Greipp PR, Garton JP et al. Primary systemic amyloidosis: comparison of melphalan/prednisone vs colchicine. Am J Med 1985; 79: 708–716.

    Article  CAS  PubMed  Google Scholar 

  4. Skinner M, Anderson J, Simms R et al. Treatment of 100 patients with primary amyloidosis: a randomized trial of melphalan, prednisone and colchicine vs colchicine only. Am J Med 1996; 100: 290–298.

    Article  CAS  PubMed  Google Scholar 

  5. Kyle RA, Gertz MA, Greipp PR et al. A trial of three regimens for primary amyloidosis: colchicine alone, melphalan and prednisone, and melphalan, prednisone and colchicine. N Engl J Med 1997; 336: 1202–1207.

    Article  CAS  PubMed  Google Scholar 

  6. Comenzo RL, Vosburgh E, Falk RH et al. Dose-intensive melphalan with blood stem-cell support for the treatment of AL (amyloid light chain) amyloidosis: survival and response in 25 patients. Blood 1998; 91: 3662–3670.

    CAS  PubMed  Google Scholar 

  7. Moreau P, Leblond V, Bourquelot P et al. Prognostic factors for survival and response after high-dose therapy and autologous stem cell transplantation in system AL amyloidosis: a report on 21 patients. Br J Hematol 1998; 101: 766–769.

    Article  CAS  Google Scholar 

  8. Gertz MA, Lacy MQ, Dispenzieri A . Treating AL amyloidosis (AL) with dose-intensive melphalan: outcomes in 102 patients. Blood 1998; 82: 324a.

    Google Scholar 

  9. Gertz MA, Lacy MQ, Dispenzieri A . Myeloablative chemotherapy with stem cell rescue for the treatment of primary systemic amyloidosis: a status report. Bone Marrow Transplant 2000; 25: 465–470.

    Article  CAS  PubMed  Google Scholar 

  10. Sanchorawala V, Wright DG, Seldin DC et al. An overview of the use of high-dose melphalan with autologous stem cell transplantation for the treatment of AL amyloidosis. Bone Marrow Transplant 2001; 28: 637–642.

    Article  CAS  PubMed  Google Scholar 

  11. Saba N, Sutton DM, Ross JH et al. High treatment-related mortality in cardiac amyloid patients undergoing autologous stem cell transplant. Bone Marrow Transplant 1999; 24: 853–855.

    Article  CAS  PubMed  Google Scholar 

  12. Dispenzieri A, Kyle RA, Lacy MQ et al. Superior survival in primary systemic amyloidosis patients undergoing peripheral blood stem cell transplantation: a case–control study. Blood 2004; 103: 3960–3963.

    Article  CAS  PubMed  Google Scholar 

  13. Disperzieri A, Lacy MQ, Kyle RA et al. Eligibility for hematopoietic stem cell transplantation for primary systemic amyloidosis is a favorable prognostic factor for survival. J Clin Oncol 19; 2001: 3350–3356.

    Google Scholar 

  14. Mollee P, Wechalekar AD, Peireira D . Autologous stem cell transplantation in primary systemic amyloidosis: the impact of selection criteria on outcome. Bone Marrow Transplant 2004; 33: 271–277.

    Article  CAS  PubMed  Google Scholar 

  15. Comenzo RL, Gertz MA . Autologous stem cell transplantation for primary systemic amyloidosis. Blood 2002; 99: 4276–4282.

    Article  CAS  PubMed  Google Scholar 

  16. Skinner M, Sanchorawala V, Seldin DC et al. High dose melphalan and autologous stem cell transplantation in patients with AL amyloidosis: an 8 year study. Ann Intern Med 2004; 140: 85–93.

    Article  CAS  PubMed  Google Scholar 

  17. Gertz MA, Blood E, Vesole DH et al. A multicenter phase 2 trial of stem cell transplantation for immunoglobulin light-chain amyloidosis (E4A97): an Eastern Cooperative Oncology Group Study. Bone Marrow Transplant 2004; 34: 149–154.

    Article  CAS  PubMed  Google Scholar 

  18. Lachmann HJ, Booth DR, Booth SE et al. Misdiagnosis of hereditary amyloidosis as AL (primary) amyloidosis. N Engl J Med 2002; 346: 1786–1791.

    Article  CAS  PubMed  Google Scholar 

  19. Dispenzieri A, Gertz MA, Klye RA et al. Prognostication of survival using cardiac troponins and N-terminal pro-brain natriuretic peptide in patients with primary systemic amyloidosis undergoing peripheral blood stem cell transplantation. Blood 2004; 104: 1881–1887.

    Article  CAS  PubMed  Google Scholar 

  20. Sanchorawala V, Wright DG, Seldin DC et al. High-dose intravenous melphalan and autologous stem cell transplantation as initial therapy or following two cycles of oral chemotherapy for the treatment of AL amyloidosis: results of a prospective randomized trial. Bone Marrow Transplant 2004; 33: 381–388.

    Article  CAS  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to D A Stewart.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Chow, L., Bahlis, N., Russell, J. et al. Autologous transplantation for primary systemic AL amyloidosis is feasible outside a major amyloidosis referral centre: the Calgary BMT Program experience. Bone Marrow Transplant 36, 591–596 (2005). https://doi.org/10.1038/sj.bmt.1705112

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/sj.bmt.1705112

Keywords

This article is cited by

Search

Quick links