Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
1999-6-22
pubmed:abstractText
From March 1994 to September 1997, 30 patients with hematological malignancies (12 ANLL, 10 CML, four ALL and four multiple myeloma) received HLA-identical allogeneic bone marrow transplants with the marrow graft selectively depleted of CD4+ lymphocytes and the CD8+ cell content adjusted to 1x10(6)/kg. Total depletion of CD4+ and partial depletion of CD8+ lymphocytes was carried out by an immunomagnetical method. All patients were considered as having high risk for developing GVHD by at least one of the following criteria: patient age >35 years; donor age >35 years; donor multiparity or marrow from an unrelated donor. Twenty-four cases received marrow from an identical sibling and six from an unrelated donor. In order to assess the role of methotrexate (MTX) in addition to cyclosporin A (CsA) after transplant, patients were randomly assigned to received either CsA alone (n = 15) or CsA plus a short course of MTX (n = 15). No case of primary graft failure was observed, but two patients developed late graft failure. Six patients presented grade II acute GVHD and no case of severe III-IV GVHD was seen. The actuarial probability of developing grade II-IV acute GVHD was 25.9+/-9.6% for the entire population. Patients receiving post-transplant CsA + MTX had significantly less probability of acute GVHD than those receiving CsA exclusively (6.7+/-6.4% vs. 50.5+/-17.8%, P = 0.03) and the schedule of post-transplant immunosuppression was the only factor associated with the incidence of acute GVHD in a multivariate analysis. The actuarial incidence of chronic GVHD for the entire population was 31.8+/-12.5, and there was no significant difference between both groups with additional prophylaxis. Four patients with CML and three with ANLL relapsed: the actuarial probability of remaining in complete remission for all patients was 53.6+/-17.3%. For patients with acute leukemia, the probability of remaining in complete remission did not differ significantly between those transplanted in first complete remission and those receiving a transplant in more advanced phases of the disease (87.5+/-11.6% vs. 72.9+/-16.5%; P = 0.44). The incidence of mixed chimerism assessed by PCR was 34%. Nineteen patients are alive between 2 and 43 months post-transplant, the probability of overall survival being 57.8+/-10.4%. Our data indicate that this method of selective T cell depletion is very effective in preventing acute GVHD in high risk patients, particularly when used in combination with post-transplant CsA + MTX.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0268-3369
pubmed:author
pubmed:issnType
Print
pubmed:volume
23
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
443-50
pubmed:dateRevised
2006-4-24
pubmed:meshHeading
pubmed-meshheading:10100557-Adolescent, pubmed-meshheading:10100557-Adult, pubmed-meshheading:10100557-Antineoplastic Combined Chemotherapy Protocols, pubmed-meshheading:10100557-Bone Marrow Transplantation, pubmed-meshheading:10100557-CD4-Positive T-Lymphocytes, pubmed-meshheading:10100557-CD8-Positive T-Lymphocytes, pubmed-meshheading:10100557-Child, pubmed-meshheading:10100557-Combined Modality Therapy, pubmed-meshheading:10100557-Female, pubmed-meshheading:10100557-Graft vs Host Disease, pubmed-meshheading:10100557-Hematologic Neoplasms, pubmed-meshheading:10100557-Histocompatibility Testing, pubmed-meshheading:10100557-Humans, pubmed-meshheading:10100557-Immunomagnetic Separation, pubmed-meshheading:10100557-Immunosuppressive Agents, pubmed-meshheading:10100557-Lymphocyte Depletion, pubmed-meshheading:10100557-Male, pubmed-meshheading:10100557-Methotrexate, pubmed-meshheading:10100557-Middle Aged, pubmed-meshheading:10100557-Transplantation, Homologous, pubmed-meshheading:10100557-Treatment Outcome
pubmed:year
1999
pubmed:articleTitle
Prevention of graft-versus-host disease in high risk patients by depletion of CD4+ and reduction of CD8+ lymphocytes in the marrow graft.
pubmed:affiliation
Department of Hematology, Hospital Reina Sofia, Córdoba, Spain.
pubmed:publicationType
Journal Article, Clinical Trial, Randomized Controlled Trial