Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
10
pubmed:dateCreated
1996-12-17
pubmed:abstractText
We have developed a quantitative reverse transcriptase-polymerase chain reaction method for the quantitation of AML1-MTG8 transcripts in patients with AML-M2 and t(8;21) in different phases of the disease. Using this method, we have tested sequential samples from 13 patients to monitor minimal residual disease and were able to show a significant increase in AML1-MTG8 transcripts level in two patients 2 and 4 months before clinical relapse. In five patients tested at presentation and then sequentially at remission, we detected a marked decrease in the level of AML1-MTG8 transcripts as the treatment progressed. Patients in long-term remission of their disease had a level of up to 1 x 10(3) AML1-MTG8 molecules/microgram RNA. Two patients tested 2 and 4 months before hematologic relapse showed a level of 0.71 x 10(5) molecules/microgram RNA and this level increased further during relapse to 0.71 x 10(7) and 2.27 x 10(5) molecules/microgram RNA, respectively. Our results show that quantitation of AML1-MTG8 transcripts by competitive polymerase chain reaction is valuable in predicting early relapse in AML with t(8;21). Identification of at-risk patients may allow treatment to be modified to include additional or alternative therapy such as bone marrow transplantation.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0006-4971
pubmed:author
pubmed:issnType
Print
pubmed:day
15
pubmed:volume
88
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
3704-9
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:8916934-Adolescent, pubmed-meshheading:8916934-Adult, pubmed-meshheading:8916934-Bone Marrow Examination, pubmed-meshheading:8916934-Chromosomes, Human, Pair 21, pubmed-meshheading:8916934-Chromosomes, Human, Pair 8, pubmed-meshheading:8916934-Core Binding Factor Alpha 2 Subunit, pubmed-meshheading:8916934-DNA-Binding Proteins, pubmed-meshheading:8916934-Disease-Free Survival, pubmed-meshheading:8916934-Female, pubmed-meshheading:8916934-Gene Expression Regulation, Leukemic, pubmed-meshheading:8916934-Humans, pubmed-meshheading:8916934-Leukemia, Myeloid, Acute, pubmed-meshheading:8916934-Male, pubmed-meshheading:8916934-Middle Aged, pubmed-meshheading:8916934-Neoplasm, Residual, pubmed-meshheading:8916934-Oncogene Proteins, Fusion, pubmed-meshheading:8916934-Polymerase Chain Reaction, pubmed-meshheading:8916934-Prognosis, pubmed-meshheading:8916934-Proto-Oncogene Proteins, pubmed-meshheading:8916934-RNA, Messenger, pubmed-meshheading:8916934-RNA, Neoplasm, pubmed-meshheading:8916934-Risk, pubmed-meshheading:8916934-Sensitivity and Specificity, pubmed-meshheading:8916934-Transcription Factors, pubmed-meshheading:8916934-Translocation, Genetic
pubmed:year
1996
pubmed:articleTitle
Monitoring of minimal residual disease by quantitative reverse transcriptase-polymerase chain reaction for AML1-MTG8 transcripts in AML-M2 with t(8; 21).
pubmed:affiliation
University Department of Haematology, Manchester Royal Infirmary, UK.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't