Abstract
We analyzed the results of a three or more drug combination as treatment for moderate or severe cGVHD developing after transplantation for thalassemia, in 45 patients with median age of 11 (range 2–26) years. Eighteen patients received a three drug regimen with cyclosporine (CsA), methylprednisolone (MP) and azathioprine (AZ) as first line therapy, 16 patients received this regimen as salvage therapy and 11 patients were given a four or five drug regimen with CsA, MP, AZ, cyclophosphamide (CY) and/or methotrexate (MTX) mainly as salvage therapy. The overall complete response (CR) rate was 77.3%, with 94% of CR in patients receiving the three drug regimen as first line, 88% in patients receiving it as salvage therapy and 36.6% in patients given the four or five drug regimen. The probability of CR in patients given the three drug regimen as first or salvage therapy or the four/five drug regimen was 89%, 53% and 30%, while the probability of survival was 89%, 65% and 58%, respectively. The incidence of treatment failure was low in our patients. Patients treated with the three drug regimen as first line therapy had less treatment-related complications than patients receiving this regimen as salvage therapy or patients given the four or five drug regimen. The main causes of treatment-related mortality (20%) were infectious complications. This retrospective study showed that a three or more drug combination is safe and effective for treatment of moderate or severe cGVHD at least in younger patients. Bone Marrow Transplantation (2001) 27, 45–51.
This is a preview of subscription content, access via your institution
Access options
Subscribe to this journal
Receive 12 print issues and online access
$259.00 per year
only $21.58 per issue
Buy this article
- Purchase on Springer Link
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout
Similar content being viewed by others
References
Lucarelli G, Galimberti M, Polchi P et al. Bone marrow transplantation in patients with thalassemia New Engl J Med 1990 322: 417–421
Gaziev D, Polchi P, Galimberti M et al. Graft versus-host disease after bone marrow transplantation for thalassemia: an analysis of incidence and risk factors Transplantation 1977 6: 854–860
Shulman HM, Sullivan KM, Weiden PL et al. Chronic graft-versus-host syndrome in man: a clinicopathological study of 20 long-term Seattle patients Am J Med 1980 69: 204–217
Beatty PG, Hansen JA, Longton GM et al. Marrow transplantation from HLA-matched unrelated donors for treatment of hematologic malignancies Transplantation 1991 2: 443–447
Morton AJ, Anasetti C, Gooley T et al. Chronic graft-versus-host disease (GVHD) following unrelated donor transplantation Blood 1997 10: 590a
Storek J, Gooley T, Siadak M et al. Allogeneic peripheral blood stem cell transplantation may be associated with a high risk of chronic graft-versus-host disease Blood 1997 12: 4705–4709
Urbano-Ispizua A, Garcia- Conde J, Brunet S et al. High incidence of chronic graft versus host disease after allogeneic peripheral blood progenitor cell transplantation Haematologica 1997 82: 683–689
Wingard JR, Piantadosi S, Vogelsang GB et al. Predictors of death from chronic graft-versus-host disease after bone marrow transplantation Blood 1989 4: 1428–1435
Sullivan KM, Witherspoon RP, Storb P et al. Prednisone and azathioprine compared with prednisone and placebo for treatment of chronic graft-v-host disease: prognostic influence of prolonged thrombocytopenia after allogeneic marrow transplantation Blood 1988 2: 546–554
Sullivan KM, Gooley T, Nims J et al. Comparison of cyclosporine (CSP), prednisone (PRED) or alternating-day CSP/PRED in patients with standard and high risk chronic graft-versus-host disease (GVHD) Blood 1990 10: 215a
Gaziev D, Galimberti M, Lucarelli G, Polchi P . Chronic graft-versus-host disease: is there an alternative to the conventional treatment? Bone Marrow Transplant 2000 25: 689–696
Lucarelli G, Clift RA, Galimberti M et al. Marrow transplantation for patients with thalassemia. Results in class 3 patients Blood 1996 80: 2082–2088
Lucarelli G, Clift RA, Galimberti M et al. Bone marrow transplantation in adult thalassemic patients Blood 1999 4: 1164–1167
Kaplan EL, Meier P . Non parametric estimation from incomplete observations J Am Stat Assoc 1958 53: 457–481
Friedman Ph . GB-STAT. Tutorial Copyright by Dynamic Microsystems: Silver Spring, MD 1998
Sullivan KM, Flowers MED, Nims J et al. Results of four regimens of salvage treatment of refractory chronic graft-versus-host disease (GVHD) Blood 1996 10: 644a
Acknowledgements
We thank Ms Law Aileen, member of our nursing staff, for linguistic assistance and all the members of our BMT Team for their exemplary care of these patients. This work has been supported by the Berloni Foundation against Thalassemia, Pesaro.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Gaziev, D., Lucarelli, G., Polchi, P. et al. A three or more drug combination as effective therapy for moderate or severe chronic graft-versus-host disease. Bone Marrow Transplant 27, 45–51 (2001). https://doi.org/10.1038/sj.bmt.1702741
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1038/sj.bmt.1702741
Keywords
This article is cited by
-
Low-dose methotrexate for the treatment of graft-versus-host disease after allogeneic hematopoietic stem cell transplantation
Bone Marrow Transplantation (2005)
-
Chronic graft-versus-host disease: clinical manifestation and therapy
Bone Marrow Transplantation (2001)