Source:http://linkedlifedata.com/resource/pubmed/id/17876770
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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0023473,
umls-concept:C0026882,
umls-concept:C0030705,
umls-concept:C0087111,
umls-concept:C0205087,
umls-concept:C0205251,
umls-concept:C0457343,
umls-concept:C0683598,
umls-concept:C0814128,
umls-concept:C0935989,
umls-concept:C1521828,
umls-concept:C1522326,
umls-concept:C1522577,
umls-concept:C1977882
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pubmed:issue |
3
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pubmed:dateCreated |
2008-2-4
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pubmed:abstractText |
The introduction of Imatinib (IM) has significantly altered the treatment for CML, although only limited follow-up results are available. As failure of Interferon-alpha had been associated with poor prognosis and results of IM-treatment in this patient group may allow earlier estimation of long-term benefits for early chronic phase patients. Therefore we prospectively analyzed the quality and duration of remissions and the rate of BCR-ABL resistance mutations occurring in patients treated with IM, if they were intolerant or refractory to interferon. Fifty-nine patients were included and median follow up is 4.75 years. Haematologic remission rate was 92% and 62% of patients achieved at least major cytogenetic remission. There were no major differences between patients failing or being refractory to IFN. Major molecular response was observed in 67% of patients evaluable. For the entire group, median PFS was 4.3 years and OS was 82% at 4.75 years. Haematologic and complete cytogenetic remissions, but not molecular responses were correlated with improved PFS and OS. In patients with progression or inadequate response, BCR-ABL kinase domain mutations were detected in 3/28 patients. IM resulted in prolonged remission rates in a substantial proportion after IFN-failure/intolerance, with no differences in these patient groups. Quality of hematologic and cytogenetic, but not molecular response was associated with duration of remissions and survival. A low rate of resistance-mutations was detected, suggesting that alternative mechanism may play an important role in disease progression.
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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/Piperazines,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Kinase Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Pyrimidines,
http://linkedlifedata.com/resource/pubmed/chemical/imatinib
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0361-8609
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pubmed:author | |
pubmed:copyrightInfo |
(c) 2007 Wiley-Liss, Inc.
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pubmed:issnType |
Print
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pubmed:volume |
83
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
178-84
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pubmed:meshHeading |
pubmed-meshheading:17876770-Adolescent,
pubmed-meshheading:17876770-Adult,
pubmed-meshheading:17876770-Aged,
pubmed-meshheading:17876770-Antineoplastic Agents,
pubmed-meshheading:17876770-Disease-Free Survival,
pubmed-meshheading:17876770-Female,
pubmed-meshheading:17876770-Humans,
pubmed-meshheading:17876770-Leukemia, Myelogenous, Chronic, BCR-ABL Positive,
pubmed-meshheading:17876770-Male,
pubmed-meshheading:17876770-Middle Aged,
pubmed-meshheading:17876770-Piperazines,
pubmed-meshheading:17876770-Protein Kinase Inhibitors,
pubmed-meshheading:17876770-Pyrimidines,
pubmed-meshheading:17876770-Retrospective Studies,
pubmed-meshheading:17876770-Survival Analysis,
pubmed-meshheading:17876770-Time Factors
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pubmed:year |
2008
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pubmed:articleTitle |
Sustained remissions and low rate of BCR-ABL resistance mutations with imatinib treatment chronic myelogenous leukemia in patients treated in late chronic phase: a 5-year follow up.
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pubmed:affiliation |
Department of Haematology/Oncology, Johannes Gutenberg-University, Mainz, Germany. g.hess@3-med.klinik.uni-mainz.de
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pubmed:publicationType |
Journal Article
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