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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1992-2-20
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pubmed:abstractText |
Essential thrombocythemia, a myeloproliferative disorder of clonal origin, is often associated with various clinical manifestations resulting from thromboembolic or hemorrhagic complications. The long-established successful method of treatment with cytotoxic agents or radioactive phosphorus has recently been superseded by interferon alpha. We treated 14 symptomatic patients with 5 x 10(6) IU recombinant interferon alpha-2b s.c. daily. 12/14 pts responded within 14-75 days. When platelet counts decreased to below 450 g/l the frequency of administration was reduced stepwise. 7 patients remained in CR during this reduction phase and treatment was stopped in 5 pts after 12-32 months. Until now, 3 of them are still in continuous good PR without any drug therapy and free of symptoms for 3+, 19+ and 36+ months. Continuous response during maintenance was associated with age, initial platelet count and time required to reduce platelet counts to less than 450 g/l.
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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 |
Jan
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pubmed:issn |
0902-4441
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
48
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
33-6
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:1730277-Adult,
pubmed-meshheading:1730277-Biopsy, Needle,
pubmed-meshheading:1730277-Blood Cell Count,
pubmed-meshheading:1730277-Bone Marrow,
pubmed-meshheading:1730277-Female,
pubmed-meshheading:1730277-Follow-Up Studies,
pubmed-meshheading:1730277-Humans,
pubmed-meshheading:1730277-Interferon-alpha,
pubmed-meshheading:1730277-Male,
pubmed-meshheading:1730277-Middle Aged,
pubmed-meshheading:1730277-Recombinant Proteins,
pubmed-meshheading:1730277-Thrombocythemia, Essential
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pubmed:year |
1992
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pubmed:articleTitle |
Remission may continue after termination of rIFN alpha-2b treatment for essential thrombocythemia.
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pubmed:affiliation |
3rd Med. Dept., Hanusch Hospital, Vienna, Austria.
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pubmed:publicationType |
Journal Article
|