Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2003-3-21
pubmed:abstractText
Real-time quantitative reverse transcription-polymerase chain reaction (Q-RT-PCR) is increasingly used to monitor responses in chronic myeloid leukaemia (CML). The peripheral blood BCR-ABL/ABL ratio, as assessed by Q-RT-PCR, has been shown to correlate with the contemporary cytogenetic response in patients receiving imatinib (Glivec, Gleevec). We have used Q-RT-PCR to monitor the early molecular response to 4 weeks and 3 months of imatinib therapy, in 47 patients with established CML. After 4 weeks of imatinib therapy, patients whose BCR-ABL/ABL ratio had fallen to less than 50% that of baseline had a significantly higher probability of achieving a major cytogenetic response after 6 months of therapy, when compared with those whose ratio did not fall by this amount (P < 0.001). Similarly, patients whose ratio at 3 months was less than 10% of that at baseline had a significantly higher probability of achieving a major cytogenetic remission at 6 months (P < 0.001). Patients who achieved these falls in their BCR-ABL/ABL ratio at either 4 weeks or 3 months had a superior progression-free survival at a median follow-up of 16.5 months (P = 0.01 and 0.003 respectively). These effects were independent of patient age and disease stage. The occurrence of peripheral blood cytopenias sufficiently severe to interrupt therapy was unrelated to progression-free survival. In conclusion, the data suggest that the early trend in the BCR-ABL/ABL ratio may be clinically useful for the early identification of patients destined to fare poorly on imatinib.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0007-1048
pubmed:author
pubmed:issnType
Print
pubmed:volume
120
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
990-9
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:12648069-Adult, pubmed-meshheading:12648069-Aged, pubmed-meshheading:12648069-Aged, 80 and over, pubmed-meshheading:12648069-Antineoplastic Agents, pubmed-meshheading:12648069-Disease-Free Survival, pubmed-meshheading:12648069-Female, pubmed-meshheading:12648069-Follow-Up Studies, pubmed-meshheading:12648069-Fusion Proteins, bcr-abl, pubmed-meshheading:12648069-Genetic Markers, pubmed-meshheading:12648069-Humans, pubmed-meshheading:12648069-Leukemia, Myelogenous, Chronic, BCR-ABL Positive, pubmed-meshheading:12648069-Male, pubmed-meshheading:12648069-Middle Aged, pubmed-meshheading:12648069-Piperazines, pubmed-meshheading:12648069-Proto-Oncogene Proteins c-abl, pubmed-meshheading:12648069-Pyrimidines, pubmed-meshheading:12648069-Reverse Transcriptase Polymerase Chain Reaction, pubmed-meshheading:12648069-Treatment Outcome
pubmed:year
2003
pubmed:articleTitle
The early molecular response to imatinib predicts cytogenetic and clinical outcome in chronic myeloid leukaemia.
pubmed:affiliation
Department of Haematology, Royal Liverpool University Hospital, UK.
pubmed:publicationType
Journal Article