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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
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pubmed:dateCreated |
1999-2-25
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pubmed:abstractText |
The objective of this study was to test the hypothesis that 13-cis-retinoic acid (CRA) and alpha-interferon (IFN-alpha) have antitumor activity in patients with early recurrence of prostate cancer measured by rising prostate-specific antigen (PSA) after local therapy, and that this activity is associated with the increase of plasma transforming growth factor beta1 (TGF-beta1). Thirty patients with a PSA > 7 ng/ml that increased >0.4 ng/ml/month after initial radiation therapy or a PSA > 2.0 ng/ml after prostatectomy were treated with 1 mg/kg/day of CRA and 3 million units of IFN-alpha administered three times per week. Patients were followed clinically with serum measurements of PSA and assessment of toxicity. Biological activity of CRA and IFN-alpha was assessed by the measurement of plasma TGF-beta1. Twenty-six percent of patients had a partial (50% decrease maintained for 1 month) or minimal (<50% decrease maintained for 1 month) biochemical response of PSA, with a median decrease of 23% (11-55%) at 3 months. Plasma TGF-beta1 levels increased with CRA and IFN-alpha therapy and correlated with a decrease in PSA; patients with a decrease in PSA had a 151% increase in TGF-beta1 compared to 27% in patients without a decrease in PSA (P = 0.04). CRA and IFN-alpha can produce transient reduction or stabilization of PSA. The measurement of plasma TGF-beta1 at 1 month of therapy correlates with changes in PSA and may represent a useful marker for the biological effect of these agents; further analysis in larger numbers of patients and methods to optimize these effects should be explored.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antineoplastic Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Interferon-alpha,
http://linkedlifedata.com/resource/pubmed/chemical/Isotretinoin,
http://linkedlifedata.com/resource/pubmed/chemical/Prostate-Specific Antigen,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Transforming Growth Factor beta,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Markers, Biological,
http://linkedlifedata.com/resource/pubmed/chemical/interferon alfa-2a
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
1078-0432
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pubmed:author |
pubmed-author:AisnerJJ,
pubmed-author:AnscherMM,
pubmed-author:CummingsK BKB,
pubmed-author:DiPaolaR SRS,
pubmed-author:GalliPP,
pubmed-author:GoodinSS,
pubmed-author:JirtleR LRL,
pubmed-author:KongF MFM,
pubmed-author:RasheedZZ,
pubmed-author:ThompsonSS,
pubmed-author:TsaiH KHK,
pubmed-author:WeissR ERE
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pubmed:issnType |
Print
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pubmed:volume |
3
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pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
1999-2004
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:9815590-Aged,
pubmed-meshheading:9815590-Aged, 80 and over,
pubmed-meshheading:9815590-Antineoplastic Agents,
pubmed-meshheading:9815590-Follow-Up Studies,
pubmed-meshheading:9815590-Humans,
pubmed-meshheading:9815590-Interferon-alpha,
pubmed-meshheading:9815590-Isotretinoin,
pubmed-meshheading:9815590-Male,
pubmed-meshheading:9815590-Middle Aged,
pubmed-meshheading:9815590-Prostate-Specific Antigen,
pubmed-meshheading:9815590-Prostatectomy,
pubmed-meshheading:9815590-Prostatic Neoplasms,
pubmed-meshheading:9815590-Recombinant Proteins,
pubmed-meshheading:9815590-Transforming Growth Factor beta,
pubmed-meshheading:9815590-Tumor Markers, Biological
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pubmed:year |
1997
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pubmed:articleTitle |
Effect of 13-cis-retinoic acid and alpha-interferon on transforming growth factor beta1 in patients with rising prostate-specific antigen.
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pubmed:affiliation |
Departments of Medicine and Surgery, Division of Urology, University of Medicine and Dentistry of New Jersey/Robert Wood Johnson Medical School, New Brunswick, New Jersey 08903-0019, USA.
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Research Support, Non-U.S. Gov't,
Multicenter Study
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