Source:http://linkedlifedata.com/resource/pubmed/id/18275431
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rdf:type | |
lifeskim:mentions |
umls-concept:C0017262,
umls-concept:C0023434,
umls-concept:C0030705,
umls-concept:C0035647,
umls-concept:C0038952,
umls-concept:C0085862,
umls-concept:C0185117,
umls-concept:C0220901,
umls-concept:C0302350,
umls-concept:C0549193,
umls-concept:C1299583,
umls-concept:C1416487,
umls-concept:C1549571,
umls-concept:C1608386,
umls-concept:C2698872,
umls-concept:C2911684
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pubmed:issue |
5
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pubmed:dateCreated |
2008-2-15
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pubmed:abstractText |
In vitro studies have demonstrated that surface expression of CD49d on chronic lymphocytic leukaemia (CLL) B cells facilitates leukaemic cell-stromal interactions by binding to fibronectin. This interaction reduces both spontaneous and drug-induced apoptosis. The present study measured CD49d expression by flow cytometry in a cohort of untreated CLL patients previously accrued to a prospective observational study and evaluated the relationship with overall survival (OS). Among the 158 CLL patients tested, the percentage of leukaemic B cells expressing CD49d ranged from 0 to 100%. When all risk factors were treated as continuous variables, CD49d expression showed moderate correlation with expression of ZAP-70 (r = 0.54; P < 0.0001) and CD38 (r = 0.58; P < 0.0001) but not %IGHV mutation. As a continuous variable, CD49d expression strongly correlated with OS (P < 0.0001). Recursive partitioning analysis suggested the 45% threshold of CD49d expression best predicted OS. Multivariate analysis, controlling for disease stage, ZAP-70, IGHV status and fluorescent in situ hybridization defects identified CD49d as an independent predictor of OS and was a better predictor of clinical outcome than ZAP-70, IGHV, or cytogenetics. This observational cohort study suggests that CLL B-cell expression of CD49d is an easily measurable and independent predictor of OS and CD49d expression in CLL. Importantly, anti-CD49d antibodies are already approved for treatment of other human diseases. Clinical testing of anti-CD49d therapy in CLL appears warranted.
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pubmed:grant |
http://linkedlifedata.com/resource/pubmed/grant/CA 113408,
http://linkedlifedata.com/resource/pubmed/grant/CA 94919,
http://linkedlifedata.com/resource/pubmed/grant/CA97274,
http://linkedlifedata.com/resource/pubmed/grant/K23 CA113408-01A1,
http://linkedlifedata.com/resource/pubmed/grant/K23 CA113408-02
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pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
1365-2141
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pubmed:author |
pubmed-author:BoneNancy DND,
pubmed-author:CallTim GTG,
pubmed-author:DewaldGordon WGW,
pubmed-author:GeyerSusan MSM,
pubmed-author:JelinekDiane FDF,
pubmed-author:KayNeil ENE,
pubmed-author:LaplantBetsyB,
pubmed-author:NowakowskiGreg SGS,
pubmed-author:ShanafeltTait DTD,
pubmed-author:TschumperRenee CRC,
pubmed-author:WitzigTom ETE,
pubmed-author:ZentClive SCS
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pubmed:issnType |
Electronic
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pubmed:volume |
140
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
537-46
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pubmed:dateRevised |
2008-7-25
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pubmed:meshHeading |
pubmed-meshheading:18275431-Adult,
pubmed-meshheading:18275431-Aged,
pubmed-meshheading:18275431-Aged, 80 and over,
pubmed-meshheading:18275431-Antigens, Neoplasm,
pubmed-meshheading:18275431-Female,
pubmed-meshheading:18275431-Humans,
pubmed-meshheading:18275431-In Situ Hybridization, Fluorescence,
pubmed-meshheading:18275431-Integrin alpha4,
pubmed-meshheading:18275431-Leukemia, Lymphocytic, Chronic, B-Cell,
pubmed-meshheading:18275431-Male,
pubmed-meshheading:18275431-Middle Aged,
pubmed-meshheading:18275431-Neoplasm Staging,
pubmed-meshheading:18275431-Prognosis,
pubmed-meshheading:18275431-Prospective Studies,
pubmed-meshheading:18275431-Survival Analysis,
pubmed-meshheading:18275431-Tumor Markers, Biological
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pubmed:year |
2008
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pubmed:articleTitle |
CD49d expression is an independent predictor of overall survival in patients with chronic lymphocytic leukaemia: a prognostic parameter with therapeutic potential.
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pubmed:affiliation |
Division of Hematology, Department of Internal Medicine, Mayo Clinic College of Medicine, Rochester, MN 55905, USA. shanafelt.tait@mayo.edu
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pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Extramural
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