Korean J Hematol.  2006 Mar;41(1):36-40. 10.5045/kjh.2006.41.1.36.

Pre-transplant Disease Status is Important for an Improved Outcome of the Second Stem Cell Transplantation in the Myeloma Patients Receiving the First Autologous Stem Cell Transplantation

Affiliations
  • 1Catholic Hemopoietic Stem Cell Transplantation Center, The Catholic University of Korea, Seoul, Korea. ckmin@catholic.ac.kr

Abstract

BACKGROUND: Double autologous stem cell transplantation (ASCT) seems to be superior to a single ASCT, at least in the patients who did not achieve a 90% response after the first transplant. An allogeneic SCT with a dose-reduced conditioning regimen after ASCT and as part of the initial therapy, might be a feasible and highly effective approach. The aim of this study was to determine the prognostic factors that are associated with the outcome of multiple myeloma (MM) patients who had received a second transplant.
METHODS
From April 1996 to December 2004, 38 MM patients, who had previously received high-dose melphalan (200 mg/m2) with autologous stem cell support, underwent a second transplant. Following the 1(st) ASCT, 24 patients received a second ASCT and 14 received a tandem reduced-intensity conditioning allogeneic stem cell transplantation (RIST) from their HLA-matched siblings.
RESULTS
The 3-year estimated PFS and overall survival (OS) from the time of the first ASCT were 25.2% and 77.6%, respectively. The median PFS and OS were 26 months (95% CI, 23~29) and 60 months (95% CI, 44~76), respectively. The disease status (a CR vs. PR or less) at the second transplant was be the most powerful factor for improving the PFS (P=0.001, hazard ratio 5.8, 95% CI 2.1~16.1).
CONCLUSION
Patients whose disease is sensitive to chemotherapy and who obtain a CR after a single transplantation might benefit the most from a second transplant.

Keyword

Multiple myeloma; Tandem stem cell transplantation; Reduced-intensity allogeneic transplantation; Autologous stem cell transplantation

MeSH Terms

Drug Therapy
Humans
Melphalan
Multiple Myeloma
Siblings
Stem Cell Transplantation*
Stem Cells*
Melphalan

Figure

  • Fig. 1 Progression-free survival of all patients (n=38) who received the first autologous stem cell transplant according to the disease status prior to the second transplant.

  • Fig. 2 Progression-free survival of patients (A; n=14) who received the reduced-intensity conditioning allogeneic stem cell transplantation and those (B; n=24) who underwent the autologous stem cell transplant according to the disease status before the second transplant.


Reference

1). Child JA., Morgan GJ., Davies FE, et al. Medical Research Council Adult Leukaemia Working Party. High-dose chemotherapy with hematopoietic stem-cell rescue for multiple myeloma. N Engl J Med. 2003. 348:1875–83.
2). Harousseau JL., Milpied N., Laporte JP, et al. Double-intensive therapy in high-risk multiple myeloma. Blood. 1992. 79:2827–33.
Article
3). Vesole DH., Barlogie B., Jagannath S, et al. High-dose therapy for refractory multiple myeloma: improved prognosis with better supportive care and double transplants. Blood. 1994. 84:950–6.
Article
4). Maloney DG., Molina AJ., Sahebi F, et al. Allografting with nonmyeloablative conditioning following cytoreductive autografts for the treatment of patients with multiple myeloma. Blood. 2003. 102:3447–54.
Article
5). Kroger N., Schwerdtfeger R., Kiehl M, et al. Autologous stem cell transplantation followed by a dose-reduced allograft induces high complete remission rate in multiple myeloma. Blood. 2002. 100:755–60.
6). Attal M., Harousseau JL., Facon T, et al. InterGroupe Francophone du Myelome. Single versus double autologous stem-cell transplantation for multiple myeloma. N Engl J Med. 2003. 349:2495–502.
Article
7). Neumann F., Graef T., Tapprich C, et al. Cyclosporine A and mycophenolate mofetil vs cyclosporine A and methotrexate for graft-versus-host disease prophylaxis after stem cell transplantation from HLA-identical siblings. Bone Marrow Transplant. 2005. 35:1089–93.
Article
8). Glucksberg H., Storb R., Fefer A, et al. Clinical manifestations of graft-versus-host disease in human recipients of marrow from HLA-matched sibling donors. Transplantation. 1974. 18:295–304.
Article
9). Shulman HM., Sullivan KM., Weiden PL, et al. Chronic graft-versus-host syndrome in man. A long-term clinicopathologic study of 20 Seattle patients. Am J Med. 1980. 69:204–17.
10). Alyea E., Weller E., Schlossman R, et al. Outcome after autologous and allogeneic stem cell transplantation for patients with multiple myeloma: impact of graft-versus-myeloma effect. Bone Marrow Transplant. 2003. 32:1145–51.
Article
11). Lahuerta JJ., Grande C., Martinez-Lopez J, et al. Grupo Espanol de Sindromes Linfoproliferativos/Trasplante Autologo de Medula Osea. Tandem transplants with different high-dose regimens improve the complete remission rates in multiple myeloma. Results of a Grupo Espanol de Sindromes Linfopro-liferativos/Trasplante Autologo de Medula Osea phase II trial. Br J Haematol. 2003. 120:296–303.
12). Alexanian R., Weber D., Giralt S, et al. Impact of complete remission with intensive therapy in patients with responsive multiple myeloma. Bone Marrow Transplant. 2001. 27:1037–43.
Article
13). Blade J., Esteve J., Rives S, et al. High-dose therapy autotransplantation/intensification vs continued standard chemotherapy in multiple myeloma in first remission. Results of a non-randomized study from a single institution. Bone Marrow Transplant. 2000. 26:845–9.
Article
14). Lokhorst HM., Schattenberg A., Cornelissen JJ, et al. Donor lymphocyte infusions for relapsed multiple myeloma after allogeneic stem-cell transplantation: predictive factors for response and long-term outcome. J Clin Oncol. 2000. 18:3031–37.
Article
15). Sarasquete ME., Garcia-Sanz R., Gonzalez D, et al. Minimal residual disease monitoring in multiple myeloma: a comparison between allelic-specific oligonucleotide real-time quantitative polymerase chain reaction and flow cytometry. Haematologica. 2005. 90:1365–72.
Full Text Links
  • KJH
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr