Linked Life Data

11843822

Source:http://linkedlifedata.com/resource/pubmed/id/11843822

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
2002-2-14
pubmed:abstractText
Thirty patients with myelodysplastic syndromes (MDS) were treated with thalidomide at 100 mg/d p.o., increased as tolerated to 400 mg/d for 12 weeks. Levels of apoptosis, macrophage number, microvessel density (MVD), tumour necrosis factor alpha (TNF-alpha), transforming growth factor beta (TGF-beta), interleukin 6 (IL-6), vascular endothelial growth factor (VEGF) and basic fibroblast growth factor (bFGF) were determined in the serum, bone marrow (BM) plasma and BM biopsies before and after therapy. Pretherapy biological characteristics of MDS patients were compared with similar studies performed in 11 normal volunteers. Ten patients demonstrated haematological improvement in the erythroid series, six becoming transfusion independent. Responders had a higher pretherapy platelet count (P < 0.048) and lower BM blasts (P < 0.013). Median time to response was 10 weeks, and four remain in remission beyond a year. Pretherapy MDS BMs showed higher MVD (P < 0.001) and TGF-beta (P < 0.03) and higher serum TNF-alpha (P < 0.008) compared with normal control subjects. After therapy, only BM TGF-beta decreased significantly (P < 0.002). Pretherapy haemoglobin was directly related to serum VEGF (P < 0.001) in responders and inversely related in non-responders (P < 0.05), suggesting the possibility that angiogenesis may be a primary pathology in the former and a consequence of anaemia-induced hypoxia in the latter. We conclude that thalidomide has important clinical and biological effects in at least a subset of MDS patients, but the precise mechanism of its action remains unknown and requires further study including a larger number of patients.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0007-1048
pubmed:author
pubmed:issnType
Print
pubmed:volume
115
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
881-94
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:11843822-Aged, pubmed-meshheading:11843822-Case-Control Studies, pubmed-meshheading:11843822-Cytokines, pubmed-meshheading:11843822-Endothelial Growth Factors, pubmed-meshheading:11843822-Female, pubmed-meshheading:11843822-Hemoglobins, pubmed-meshheading:11843822-Humans, pubmed-meshheading:11843822-Immunosuppressive Agents, pubmed-meshheading:11843822-Lymphokines, pubmed-meshheading:11843822-Male, pubmed-meshheading:11843822-Myelodysplastic Syndromes, pubmed-meshheading:11843822-Platelet Count, pubmed-meshheading:11843822-Remission Induction, pubmed-meshheading:11843822-Thalidomide, pubmed-meshheading:11843822-Transforming Growth Factor alpha, pubmed-meshheading:11843822-Transforming Growth Factor beta, pubmed-meshheading:11843822-Vascular Endothelial Growth Factor A, pubmed-meshheading:11843822-Vascular Endothelial Growth Factors
pubmed:year
2001
pubmed:articleTitle
The clinical and biological effects of thalidomide in patients with myelodysplastic syndromes.
pubmed:affiliation
MDS Center, Section of Myeloid Diseases, Rush Presbyterian St Luke's Medical Center, 2242 West Harrison Street, Suite 108, Chicago, IL 60612, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't