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Deep sequencing of BCR-ABL1 kinase domain mutations in chronic myeloid leukemia patients with resistance to tyrosine kinase inhibitors    
Yazarlar
Yücel Erbilgin
Türkiye
Ahmet Emre Eskazan
Türkiye
Ng Özden Hatırnaz
Türkiye
Ayse Salihoglu
Türkiye
Tugrul Elverdi
Türkiye
Sinem Fırtına
İstinye Üniversitesi, Türkiye
Orcun Tasar
Türkiye
Dr. Öğr. Üyesi Sevcan MERCAN Dr. Öğr. Üyesi Sevcan MERCAN
Kafkas Üniversitesi, Türkiye
Sinem Sisko
Türkiye
Khusan Khodzhaev
Türkiye
Seniz Ongoren
Türkiye
Muhlis Cem Ar
İstanbul Üniversitesi-Cerrahpaşa, Türkiye
Zafer Baslar
Türkiye
Teoman Soysal
İstanbul Üniversitesi-Cerrahpaşa, Türkiye
Müge Sayitoğlu
İstanbul Üniversitesi, Türkiye
Uğur Özbek
Acıbadem Mehmet Ali Aydınlar Üniversitesi, Türkiye
Özet
Tyrosine kinase inhibitor (TKI) therapy is the current treatment of choice for patients with chronic phase chronic myeloid leukemia (CML) leading to rapid and durable hematological as well as molecular responses. However, emergence of resistance to TKIs has been the major obstacle to treatment success on long term. In this regard kinase domain mutations are the most common mechanism of therapy failure. In this study, we analyzed peripheral blood samples from 17 CML patients who had developed resistance to various TKIs by using next-generation sequencing parallel to Sanger sequencing. BCR-ABL1 kinase domain mutations have been found in 59% of the cohort. Our results demonstrate that next-generation sequencing results in a higher mutational detection rate than reported with conventional sequencing methodology. Furthermore, it showed the clonal diversity more accurately.
Anahtar Kelimeler
Chronic myeloid leukemia | drug resistance | next-generation sequencing | tyrosine kinase inhibitor
Makale Türü Özgün Makale
Makale Alt Türü SSCI, AHCI, SCI, SCI-Exp dergilerinde yayımlanan tam makale
Dergi Adı Leukemia Lymphoma
Dergi ISSN 1042-8194
Dergi Tarandığı Indeksler SCI-Expanded
Dergi Grubu Q2
Makale Dili İngilizce
Basım Tarihi 01-2019
Cilt No 60
Sayı 1
Sayfalar 200 / 207
Doi Numarası 10.1080/10428194.2018.1473573