pubmed-article:17876770 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:17876770 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
pubmed-article:17876770 | lifeskim:mentions | umls-concept:C0087111 | lld:lifeskim |
pubmed-article:17876770 | lifeskim:mentions | umls-concept:C0023473 | lld:lifeskim |
pubmed-article:17876770 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
pubmed-article:17876770 | lifeskim:mentions | umls-concept:C1522577 | lld:lifeskim |
pubmed-article:17876770 | lifeskim:mentions | umls-concept:C0814128 | lld:lifeskim |
pubmed-article:17876770 | lifeskim:mentions | umls-concept:C0935989 | lld:lifeskim |
pubmed-article:17876770 | lifeskim:mentions | umls-concept:C1977882 | lld:lifeskim |
pubmed-article:17876770 | lifeskim:mentions | umls-concept:C0683598 | lld:lifeskim |
pubmed-article:17876770 | lifeskim:mentions | umls-concept:C1521828 | lld:lifeskim |
pubmed-article:17876770 | lifeskim:mentions | umls-concept:C0205251 | lld:lifeskim |
pubmed-article:17876770 | lifeskim:mentions | umls-concept:C1522326 | lld:lifeskim |
pubmed-article:17876770 | lifeskim:mentions | umls-concept:C0205087 | lld:lifeskim |
pubmed-article:17876770 | lifeskim:mentions | umls-concept:C0457343 | lld:lifeskim |
pubmed-article:17876770 | pubmed:issue | 3 | lld:pubmed |
pubmed-article:17876770 | pubmed:dateCreated | 2008-2-4 | lld:pubmed |
pubmed-article:17876770 | 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. | lld:pubmed |
pubmed-article:17876770 | pubmed:language | eng | lld:pubmed |
pubmed-article:17876770 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17876770 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:17876770 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17876770 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17876770 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17876770 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17876770 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17876770 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:17876770 | pubmed:month | Mar | lld:pubmed |
pubmed-article:17876770 | pubmed:issn | 0361-8609 | lld:pubmed |
pubmed-article:17876770 | pubmed:author | pubmed-author:MeyerRalf GRG | lld:pubmed |
pubmed-article:17876770 | pubmed:author | pubmed-author:HuberChristop... | lld:pubmed |
pubmed-article:17876770 | pubmed:author | pubmed-author:HessGeorgG | lld:pubmed |
pubmed-article:17876770 | pubmed:author | pubmed-author:SchuchBrigitt... | lld:pubmed |
pubmed-article:17876770 | pubmed:author | pubmed-author:BechtholdKatj... | lld:pubmed |
pubmed-article:17876770 | pubmed:author | pubmed-author:El-KholyIlseI | lld:pubmed |
pubmed-article:17876770 | pubmed:copyrightInfo | (c) 2007 Wiley-Liss, Inc. | lld:pubmed |
pubmed-article:17876770 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:17876770 | pubmed:volume | 83 | lld:pubmed |
pubmed-article:17876770 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:17876770 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:17876770 | pubmed:pagination | 178-84 | lld:pubmed |
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pubmed-article:17876770 | pubmed:year | 2008 | lld:pubmed |
pubmed-article:17876770 | 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. | lld:pubmed |
pubmed-article:17876770 | pubmed:affiliation | Department of Haematology/Oncology, Johannes Gutenberg-University, Mainz, Germany. g.hess@3-med.klinik.uni-mainz.de | lld:pubmed |
pubmed-article:17876770 | pubmed:publicationType | Journal Article | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:17876770 | lld:pubmed |