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dc.contributor.authorHaznedaroglu, Ibrahim C.
dc.date.accessioned2019-12-10T11:15:01Z
dc.date.available2019-12-10T11:15:01Z
dc.date.issued2014
dc.identifier.issn2035-3006
dc.identifier.urihttps://doi.org/10.4084/MJHID.2014.009
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3894837/
dc.identifier.urihttp://hdl.handle.net/11655/15191
dc.description.abstractThe aim of oral tyrosine kinase inhibitor (TKI) treatment in chronic myeloid leukemia (CML) is to get ideal hematological, cytogenetic, molecular responses at the critical time points. The depth of the response obtained with TKI and the time to achieve this response are both important in predicting the prognosis in patients with CML. The high efficacy of the TKI treatment of CML has prompted the need for accurate methods to monitor response at levels below the landmark of CCyR. Quantification of BCR-ABL transcripts has proven to be the most sensitive method available and has shown prognostic impact with regard to progression-free survival. European LeukemiaNet (ELN) molecular program harmonized the reporting of results according to the IS (International harmonization of Scale) in Europe. The aim of this review is to outline monitoring the response to optimal TKI treatment based on the ELN CML 2013 recommendations from the clinical point of view as a physician. Careful cytogenetic and molecular monitoring could help to select the most convenient TKI drug and to optimize TKI treatment. Excessive monitoring may have an economic cost, but failure to optimize TKI treatment may result in CML disease acceleration and death.
dc.relation.isversionof10.4084/MJHID.2014.009
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleMonitoring The Response To Tyrosine Kinase Inhibitor (Tki) Treatment In Chronic Myeloid Leukemia (Cml)
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalMediterranean Journal of Hematology and Infectious Diseases
dc.contributor.departmentİç Hastalıkları
dc.identifier.volume6
dc.identifier.issue1
dc.description.indexPubMed
dc.description.indexScopus


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