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
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 |