Cargando…
Allogeneic Hematopoietic Cell Transplantation in Patients with Myelodysplastic Syndrome and Concurrent Lymphoid Malignancy
Allogeneic hematopoietic cell transplantation (HCT) can be curative for both myelodysplastic syndromes (MDS) and lymphoid malignancies. Little is known about the efficacy of allogeneic HCT in patients in whom both myeloid and lymphoid disorders are present at the time of HCT. We analyzed outcomes in...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3237793/ https://www.ncbi.nlm.nih.gov/pubmed/21909142 http://dx.doi.org/10.1038/bmt.2011.180 |
_version_ | 1782218938681131008 |
---|---|
author | Zimmerman, Zachary Scott, Bart L. Gopal, Ajay K. Sandmaier, Brenda M. Maloney, David G. Deeg, H. Joachim |
author_facet | Zimmerman, Zachary Scott, Bart L. Gopal, Ajay K. Sandmaier, Brenda M. Maloney, David G. Deeg, H. Joachim |
author_sort | Zimmerman, Zachary |
collection | PubMed |
description | Allogeneic hematopoietic cell transplantation (HCT) can be curative for both myelodysplastic syndromes (MDS) and lymphoid malignancies. Little is known about the efficacy of allogeneic HCT in patients in whom both myeloid and lymphoid disorders are present at the time of HCT. We analyzed outcomes in 21 patients with MDS and concurrent lymphoid malignancy when undergoing allogeneic HCT. Seventeen patients had received extensive prior cytotoxic chemotherapy, including autologous HCT in seven, for non-Hodgkin lymphoma (NHL, n=7), Hodgkin lymphoma (HL, n=2), chronic lymphocytic leukemia (CLL, n=5), NHL plus HL (n=1), multiple myeloma (n=1), or T-cell acute lymphocytic leukemia (ALL) (n=1), and had, presumably, developed MDS as a consequence of therapy. Four previously untreated patients had CLL. Nineteen patients were conditioned with high-dose (n=14) or reduced-intensity regimens (n=5), and transplanted from HLA-matched or one antigen/allele mismatched related (n=10) or unrelated (n=9) donors; two patients received HLA-haploidentical related transplants following conditioning with a modified conditioning regimen. Currently, 2 of 4 previously untreated, and 2 of 17 previously treated patients are surviving in remission of both MDS and lymphoid malignancies. However, the high non-relapse mortality among previously treated patients, even with reduced-intensity conditioning regimens, indicates that new transplant strategies need to be developed. |
format | Online Article Text |
id | pubmed-3237793 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
record_format | MEDLINE/PubMed |
spelling | pubmed-32377932012-12-01 Allogeneic Hematopoietic Cell Transplantation in Patients with Myelodysplastic Syndrome and Concurrent Lymphoid Malignancy Zimmerman, Zachary Scott, Bart L. Gopal, Ajay K. Sandmaier, Brenda M. Maloney, David G. Deeg, H. Joachim Bone Marrow Transplant Article Allogeneic hematopoietic cell transplantation (HCT) can be curative for both myelodysplastic syndromes (MDS) and lymphoid malignancies. Little is known about the efficacy of allogeneic HCT in patients in whom both myeloid and lymphoid disorders are present at the time of HCT. We analyzed outcomes in 21 patients with MDS and concurrent lymphoid malignancy when undergoing allogeneic HCT. Seventeen patients had received extensive prior cytotoxic chemotherapy, including autologous HCT in seven, for non-Hodgkin lymphoma (NHL, n=7), Hodgkin lymphoma (HL, n=2), chronic lymphocytic leukemia (CLL, n=5), NHL plus HL (n=1), multiple myeloma (n=1), or T-cell acute lymphocytic leukemia (ALL) (n=1), and had, presumably, developed MDS as a consequence of therapy. Four previously untreated patients had CLL. Nineteen patients were conditioned with high-dose (n=14) or reduced-intensity regimens (n=5), and transplanted from HLA-matched or one antigen/allele mismatched related (n=10) or unrelated (n=9) donors; two patients received HLA-haploidentical related transplants following conditioning with a modified conditioning regimen. Currently, 2 of 4 previously untreated, and 2 of 17 previously treated patients are surviving in remission of both MDS and lymphoid malignancies. However, the high non-relapse mortality among previously treated patients, even with reduced-intensity conditioning regimens, indicates that new transplant strategies need to be developed. 2011-09-12 2012-06 /pmc/articles/PMC3237793/ /pubmed/21909142 http://dx.doi.org/10.1038/bmt.2011.180 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Zimmerman, Zachary Scott, Bart L. Gopal, Ajay K. Sandmaier, Brenda M. Maloney, David G. Deeg, H. Joachim Allogeneic Hematopoietic Cell Transplantation in Patients with Myelodysplastic Syndrome and Concurrent Lymphoid Malignancy |
title | Allogeneic Hematopoietic Cell Transplantation in Patients with Myelodysplastic Syndrome and Concurrent Lymphoid Malignancy |
title_full | Allogeneic Hematopoietic Cell Transplantation in Patients with Myelodysplastic Syndrome and Concurrent Lymphoid Malignancy |
title_fullStr | Allogeneic Hematopoietic Cell Transplantation in Patients with Myelodysplastic Syndrome and Concurrent Lymphoid Malignancy |
title_full_unstemmed | Allogeneic Hematopoietic Cell Transplantation in Patients with Myelodysplastic Syndrome and Concurrent Lymphoid Malignancy |
title_short | Allogeneic Hematopoietic Cell Transplantation in Patients with Myelodysplastic Syndrome and Concurrent Lymphoid Malignancy |
title_sort | allogeneic hematopoietic cell transplantation in patients with myelodysplastic syndrome and concurrent lymphoid malignancy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3237793/ https://www.ncbi.nlm.nih.gov/pubmed/21909142 http://dx.doi.org/10.1038/bmt.2011.180 |
work_keys_str_mv | AT zimmermanzachary allogeneichematopoieticcelltransplantationinpatientswithmyelodysplasticsyndromeandconcurrentlymphoidmalignancy AT scottbartl allogeneichematopoieticcelltransplantationinpatientswithmyelodysplasticsyndromeandconcurrentlymphoidmalignancy AT gopalajayk allogeneichematopoieticcelltransplantationinpatientswithmyelodysplasticsyndromeandconcurrentlymphoidmalignancy AT sandmaierbrendam allogeneichematopoieticcelltransplantationinpatientswithmyelodysplasticsyndromeandconcurrentlymphoidmalignancy AT maloneydavidg allogeneichematopoieticcelltransplantationinpatientswithmyelodysplasticsyndromeandconcurrentlymphoidmalignancy AT deeghjoachim allogeneichematopoieticcelltransplantationinpatientswithmyelodysplasticsyndromeandconcurrentlymphoidmalignancy |