全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Frequency and Outcome of Graft versus Host Disease after Stem Cell Transplantation: A Six-Year Experience from a Tertiary Care Center in Pakistan

DOI: 10.1155/2013/232519

Full-Text   Cite this paper   Add to My Lib

Abstract:

Objective. The objective of this study was to evaluate the frequency and outcome of graft versus host disease after stem cell transplantation for various haematological disorders in Pakistan. Materials and Methods. Pretransplant workup of the patient and donor was performed. Mobilization was done with G-CSF 300?μg twice daily for five day. Standard GvHD prophylaxis was done with methotrexate 15?mg/m2 on day +1 followed by 10?mg/m2 on days +3 and +6 and cyclosporine. Grading was done according to the Glucksberg classification. Results. A total of 153 transplants were done from April 2004 to December 2011. Out of these were allogeneic transplants. There were females and males. The overall frequency of any degree of graft versus host disease was 34%. Acute GvHD was present in patients while had chronic GvHD. Grade II GvHD was present in patients while grade III and IV GvHD was seen in patients each. Acute myeloid leukemia and chronic myeloid leukemia were most commonly associated with GvHD. The mortality in acute and chronic GvHD was 8.8% and 12% respectively. Conclusion. The frequency of graft versus host disease in this study was 34% which is lower compared to international literature. The decreased incidence can be attributed to reduced diversity of histocompatibility antigens in our population. 1. Introduction Allogeneic haemopoietic stem cell transplant is an established treatment modality for many malignant and non-malignant conditions [1]. Its use over the last decade has extensively expanded which includes nonmyeloablative transplant, donor lymphocyte infusions, and umbilical cord blood transplant [2, 3]. As the numbers of procedures continue to increase with 25,000 transplants being performed annually, the survival benefit, however, is complicated by graft versus host disease (GvHD) leading to significant morbidity, mortality, and limitation of its usage [4]. Most of the laboratories in the world have adopted the high-resolution testing modality for human leukocyte antigen (HLA) typing. Every conditioning protocol incorporates the use of immunosuppression most commonly with cyclosporine and methotrexate. Despite these measures, GvHD remains an important cause of transplant-related mortality and morbidity leading to limitation of its usage [5]. Approximately 30 years ago, the prerequisites of acute GvHD were described by Billingham. These included immunologically competent cells in sufficient numbers to be present in the graft. The host to possess transplant isoantigens not present in the graft and its immune system should be incapable of mounting

References

[1]  F. R. Appelbaum, “Haematopoietic cell transplantation as immunotherapy,” Nature, vol. 411, no. 6835, pp. 385–389, 2001.
[2]  A. Urbano-Ispizua, “Risk assessment in haematopoietic stem cell transplantation: stem cell source,” Best Practice and Research Clinical Haematology, vol. 20, no. 2, pp. 265–280, 2007.
[3]  J. Aschan, “Risk assessment in haematopoietic stem cell transplantation: conditioning,” Best Practice and Research Clinical Haematology, vol. 20, no. 2, pp. 295–310, 2007.
[4]  J. L. M. Ferrara and P. Reddy, “Pathophysiology of graft-versus-host disease,” Seminars in Hematology, vol. 43, no. 1, pp. 3–10, 2006.
[5]  D. Couriel, H. Caldera, R. Champlin, and K. Komanduri, “Acute graft-versus-host disease: pathophysiology, clinical manifestations, and management,” Cancer, vol. 101, no. 9, pp. 1936–1946, 2004.
[6]  L. M. Ball and R. M. Egeler, “Acute GvHD: pathogenesis and classification,” Bone Marrow Transplantation, vol. 41, supplement 2, pp. S58–S64, 2008.
[7]  H. M. Shulman, K. M. Sullivan, and P. L. Weiden, “Chronic Graft-Versus-Host syndrome in man. A long-term clinicopathologic study of 20 Seattle patients,” The American Journal of Medicine, vol. 69, no. 2, pp. 204–217, 1980.
[8]  A. C. Vigorito, P. V. Campregher, B. E. Storer et al., “Evaluation of NIH consensus criteria for classification of late acute and chronic GVHD,” Blood, vol. 114, no. 3, pp. 702–708, 2009.
[9]  N. Flomenberg, L. A. Baxter-Lowe, D. Confer et al., “Impact of HLA class I and class II high-resolution matching on outcomes of unrelated donor bone marrow transplantation: HLA-C mismatching is associated with a strong adverse effect on transplantation outcome,” Blood, vol. 104, no. 7, pp. 1923–1930, 2004.
[10]  P. J. Martin, G. Schoch, L. Fisher et al., “A retrospective analysis of therapy for acute graft-verus-host disease: initial treatment,” Blood, vol. 76, no. 8, pp. 1464–1472, 1990.
[11]  J.-Y. Cahn, J. P. Klein, S. J. Lee et al., “Prospective evaluation of 2 acute graft-versus-host (GVHD) grading systems: a joint Société Fran?aise de Greffe de Mo?lle et Th?rapie Cellulaire (SFGM-TC), Dana Farber Cancer Institute (DFCI), and International Bone Marrow Transplant Registry (IBMTR) prospective study,” Blood, vol. 106, no. 4, pp. 1495–1500, 2005.
[12]  T. Teshima, T. A. Wynn, R. J. Soiffer, K.-I. Matsuoka, and P. J. Martin, “Chronic Graft-versus-Host Disease: how Can We Release Prometheus?” Biology of Blood and Marrow Transplantation, vol. 14, no. 1, pp. 142–150, 2008.
[13]  K. M. Sullivan, H. M. Shulman, and R. Storb, “Chronic graft-versus-host disease in 52 patients: adverse natural course and successful treatment with combination immunosuppression,” Blood, vol. 57, no. 2, pp. 267–276, 1981.
[14]  A. H. Filipovich, D. Weisdorf, S. Pavletic et al., “National Institutes of Health Consensus Development Project on criteria for clinical trials in chronic graft-versus-host disease: I. diagnosis and staging working group report,” Biology of Blood and Marrow Transplantation, vol. 11, no. 12, pp. 945–956, 2005.
[15]  J. M. Rowe, N. Ciobanu, J. Ascensao et al., “Recommended guidelines for the management of autologous and allogeneic bone marrow transplantation: a report from the Eastern Cooperative Oncology Group (ECOG),” Annals of Internal Medicine, vol. 120, no. 2, pp. 143–158, 1994.
[16]  P. Sodani, D. Gaziev, P. Polchi et al., “New approach for bone marrow transplantation in patients with class 3 thalassemia aged younger than 17 years,” Blood, vol. 104, no. 4, pp. 1201–1203, 2004.
[17]  D. Przepiorka, D. Weisdorf, P. Martin et al., “Consensus conference on acute GVHD grading,” Bone Marrow Transplantation, vol. 15, no. 6, pp. 825–828, 1995.
[18]  U. Platzbecker, G. Ehninger, and M. Bornh?user, “Allogeneic transplantation of CD34+ selected hematopoietic cells —clinical problems and current challenges,” Leukemia and Lymphoma, vol. 45, no. 3, pp. 447–453, 2004.
[19]  A. M. Marmont, M. M. Horowitz, R. P. Gale et al., “T-cell depletion of HLA-identical transplants in leukemia,” Blood, vol. 78, no. 8, pp. 2120–2130, 1991.
[20]  S. S. B. Randolph, T. A. Gooley, E. H. Warren, F. R. Appelbaum, and S. R. Riddell, “Female donors contribute to a selective graft-versus-leukemia effect in male recipients of HLA-matched, related hematopoietic stem cell transplants,” Blood, vol. 103, no. 1, pp. 347–352, 2004.
[21]  M. E. D. Flowers, Y. Inamoto, P. A. Carpenter et al., “Comparative analysis of risk factors for acute graft-versus-host disease and for chronic graft-versus-host disease according to National Institutes of Health consensus criteria,” Blood, vol. 117, no. 11, pp. 3214–3219, 2011.
[22]  M. Kondo, S. Kojima, K. Horibe, K. Kato, and T. Matsuyama, “Risk factors for chronic graft-versus-host disease after allogeneic stem cell transplantation in children,” Bone Marrow Transplantation, vol. 27, no. 7, pp. 727–730, 2001.
[23]  E. W. Petersdorf, G. M. Longton, C. Anasetti et al., “The significance of HLA-DRB1 matching on clinical outcome after HLA-A, B, DR identical unrelated donor marrow transplantation,” Blood, vol. 86, no. 4, pp. 1606–1613, 1995.
[24]  P. Loiseau, M. Busson, M.-L. Balere et al., “HLA association with hematopoietic stem cell transplantation outcome: the number of mismatches at HLA-A, -B, -C, -DRB1, or -DQB1 is strongly associated with overall survival,” Biology of Blood and Marrow Transplantation, vol. 13, no. 8, pp. 965–974, 2007.
[25]  K. Hashmi, B. Khan, P. Ahmed et al., “Graft versus host disease in allogeneic stem cell transplantation —3 1/2 Years experience,” Journal of the Pakistan Medical Association, vol. 55, no. 10, pp. 423–427, 2005.
[26]  A. Ghavamzadeh, K. Alimogaddam, M. Jahani et al., “Stem cell transplantation; Iranian experience,” Archives of Iranian Medicine, vol. 12, no. 1, pp. 69–72, 2009.
[27]  D.-H. Liu, X.-S. Zhao, Y.-J. Chang et al., “The impact of graft composition on clinical outcomes in pediatric patients undergoing unmanipulated HLA-mismatched/haploidentical hematopoietic stem cell transplantation,” Pediatric Blood and Cancer, vol. 57, no. 1, pp. 135–141, 2011.
[28]  P. J. Shaw, F. Kan, K. W. Ahn et al., “Outcomes of pediatric bone marrow transplantation for leukemia and myelodysplasia using matched sibling, mismatched related, or matched unrelated donors,” Blood, vol. 116, no. 19, pp. 4007–4015, 2010.
[29]  M. L. Sorror, B. M. Sandmaier, B. E. Storer et al., “Long-term outcomes among older patients following nonmyeloablative conditioning and allogeneic hematopoietic cell transplantation for advanced hematologic malignancies,” Journal of the American Medical Association, vol. 306, no. 17, pp. 1874–1883, 2011.
[30]  O. G. Cantu-Rodriguez, C. H. Gutierrez-Aguirre, J. C. Jaime-Perez, O. R. Trevino-Montemayor, S. A. Martinez-Cabriales, A. Gomez-Pena, et al., “Low incidence and severity of graft-versus-host disease after outpatient allogeneic peripheral blood stem cell transplantation employing a reduced-intensity conditioning,” European Journal of Haematology, vol. 87, no. 6, pp. 521–530, 2011.
[31]  Y.-J. Chang, C.-L. Weng, L.-X. Sun, and Y.-T. Zhao, “Allogeneic bone marrow transplantation compared to peripheral blood stem cell transplantation for the treatment of hematologic malignancies: a meta-analysis based on time-to-event data from randomized controlled trials,” Annals of Hematology, vol. 91, no. 3, pp. 427–437, 2012.
[32]  J. Auberger, J. Clausen, B. Kircher, G. Kropshofer, B. Lindner, and D. Nachbaur, “Allogeneic bone marrow vs. peripheral blood stem cell transplantation: a long-term retrospective single-center analysis in 329 patients,” The European Journal of Haematology, vol. 87, no. 6, pp. 531–538, 2011.
[33]  A. Gratwohl, R. Brand, F. Frassoni et al., “Cause of death after allogeneic haematopoietic stem cell transplantation (HSCT) in early leukaemias: an EBMT analysis of lethal infectious complications and changes over calendar time,” Bone Marrow Transplantation, vol. 36, no. 9, pp. 757–769, 2005.

Full-Text

Contact Us

[email protected]

QQ:3279437679

WhatsApp +8615387084133