rdf:type |
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lifeskim:mentions |
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pubmed:issue |
7
|
pubmed:dateCreated |
2005-6-1
|
pubmed:abstractText |
We present our first experiences with determination of minimal residual disease (MRD) based on patient specific Flt3-ITD (internal tandem duplication) mutations. We analysed MRD status of 11 AML patients in a retrospective investigation and its potential impact on the follow up of these patients. In five out of six patients with a positive Flt3-ITD based MRD status a relapse of AML was observed in the follow up while one patient lacks a clinical relapse so far. In contrast, four out of five patients with a negative MRD status remain free of disease. One of these patients relapsed with a switch of FAB subtype including loss of Flt3-ITD mutation. Furthermore, in one patient we could identify a Flt3-ITT (internal tandem triplication mutation).
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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 |
Jul
|
pubmed:issn |
0145-2126
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
29
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
849-53
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:15921740-Adult,
pubmed-meshheading:15921740-Bone Marrow,
pubmed-meshheading:15921740-Female,
pubmed-meshheading:15921740-Gene Duplication,
pubmed-meshheading:15921740-Humans,
pubmed-meshheading:15921740-Karyotyping,
pubmed-meshheading:15921740-Leukemia, Myeloid, Acute,
pubmed-meshheading:15921740-Male,
pubmed-meshheading:15921740-Middle Aged,
pubmed-meshheading:15921740-Mutation,
pubmed-meshheading:15921740-Neoplasm, Residual,
pubmed-meshheading:15921740-Proto-Oncogene Proteins,
pubmed-meshheading:15921740-Receptor Protein-Tyrosine Kinases,
pubmed-meshheading:15921740-Recurrence,
pubmed-meshheading:15921740-Retrospective Studies,
pubmed-meshheading:15921740-Treatment Outcome,
pubmed-meshheading:15921740-fms-Like Tyrosine Kinase 3
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pubmed:year |
2005
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pubmed:articleTitle |
Minimal residual disease based on patient specific Flt3-ITD and -ITT mutations in acute myeloid leukemia.
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pubmed:affiliation |
Department of Internal Medicine II Oncology and Hematology, Friedrich Schiller University, Erlanger Allee 101, 07740 Jena, Germany. sebastian.scholl@med.uni-jena.de
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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