YYÜ GCRIS Basic veritabanının içerik oluşturulması ve kurulumu Research Ecosystems (https://www.researchecosystems.com) tarafından devam etmektedir. Bu süreçte gördüğünüz verilerde eksikler olabilir.
 

Imatinib Mesylate in First-Line Treatment of Chronic Myeloid Leukemia

dc.contributor.author Ekinci, Ömer
dc.contributor.author Kızılkaya, İsmet
dc.date.accessioned 2025-05-10T17:52:21Z
dc.date.available 2025-05-10T17:52:21Z
dc.date.issued 2019
dc.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
dc.department-temp Firat Üni̇versi̇tesi̇,Van Yüzüncü Yil Üni̇versi̇tesi̇ en_US
dc.description.abstract Objective: Chronic myeloid leukemia (CML) is a myeloproliferative disease characterized by clonal proliferation of myeloid cells. Inthis study we aimed to present our experience in patients with CML who used imatinib mesylate, a tyrosine kinase inhibitor (TKI).Aim: Sixty nine patients who were diagnosed with CML and were treated with first-generation TKI ( in the form of imatinib mesylate)as initial treatment between 2006 and 2018 were included in this retrospective study. The demographic characteristics, responserates (hematologic, cytogenetic and molecular), adverse events and overall survival (OS) rates were retrospectively analyzed.Results: There were 28 male and 41 female patients with a median age of 49.3. Hematologic, cytogenetic and molecular responsesto TKI treatment were evaluated according to the 2013 guidelines of European Leukemia Net (ELN). The complete hematologicresponse (CHR) rate at three months was 97.1%, the complete cytogenetic response (CCR) rate at 12 months was 73.4%, and themajor molecular response (MMR) at 18 months was 77.8%. The most common adverse events were cytopenia (13%), edema (10.1%),nausea/vomiting (7.2%), and musculoskeletal pain (5.8%). The mean follow-up period was 40.4 months for all CML patients, with anoverall survival (OS) rate of 84.6% during follow-up.Conclusion: As a real life data in our population, our results were consistent with those reported in the literature. Drug-relatedadverse events were minimal and tolerable. Long-term survival and disease-free survival can be achieved with proper cytogeneticand molecular monitoring under imatinib treatment and, if necessary, a change in medication. en_US
dc.identifier.doi 10.5455/annalsmedres.2019.08.449
dc.identifier.endpage 1743 en_US
dc.identifier.issn 2636-7688
dc.identifier.issue 9 en_US
dc.identifier.scopusquality N/A
dc.identifier.startpage 1737 en_US
dc.identifier.trdizinid 318021
dc.identifier.uri https://doi.org/10.5455/annalsmedres.2019.08.449
dc.identifier.uri https://search.trdizin.gov.tr/en/yayin/detay/318021/imatinib-mesylate-in-first-line-treatment-of-chronic-myeloid-leukemia
dc.identifier.uri https://hdl.handle.net/20.500.14720/18306
dc.identifier.volume 26 en_US
dc.identifier.wosquality N/A
dc.language.iso en en_US
dc.relation.ispartof Annals of Medical Research en_US
dc.relation.publicationcategory Makale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanı en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Tıbbi Araştırmalar Deneysel en_US
dc.subject Genel Ve Dahili Tıp en_US
dc.subject Hematoloji en_US
dc.title Imatinib Mesylate in First-Line Treatment of Chronic Myeloid Leukemia en_US
dc.type Article en_US

Files