Research Article

A retrospective evaluation of chronic myeloid leukemia patients treated with imatinib

Volume: 64 Number: 3 September 8, 2025
TR EN

A retrospective evaluation of chronic myeloid leukemia patients treated with imatinib

Abstract

Aim: The study aimed to evaluate the clinical outcomes of chronic myeloid leukemia (CML) patients treated with imatinib at Ege University Department of Hematology over an eight-year period. Material and Methods: This observational retrospective study included 72 chronic phase CML patients aged over 18 years, treated with imatinib. Patients in the blastic or accelerated phases were excluded. Clinical, socio-demographic, and laboratory data were collected from the patient files. Patients were divided as early chronic phase (treated with imatinib within 6 months of diagnosis) and late chronic phase (started imatinib therapy at least 6 months after diagnosis). Hematologic, molecular, and cytogenetic responses at 3, 6, 12, and 18 months of imatinib therapy were recorded. Data analysis was performed using SPSS version 16.0. Results: Hematologic response at 3 months with imatinib was 80.5%, increasing to 94.7% at following months. Complete cytogenetic remission (CCyR) was achieved in 80% of patients within the 12 months. Overall response rate was 83.3% with a median follow-up of 10 years. The incidence of adverse events was 30.5%, compromising mostly non-hematologic toxicities such as edema and skin changes. Despite the adverse events, imatinib demonstrated significant clinical benefits comparable to second-generation tyrosine kinase inhibitors (TKIs). Conclusion: Over a decade has passed since our study was designed, yet imatinib continues to be a cornerstone in the treatment of chronic myeloid leukemia (CML). Imatinib is still an effective frontline therapy for CML, with high response rates, cost-effectivity and manageable toxicities.

Keywords

References

  1. Rudolf Virchow (1821-1902). CA Cancer J Clin. 1975;25(2):91-92.
  2. Bartram CR, de Klein A, Hagemeijer A, et al. Translocation of c-ab1 oncogene correlates with the presence of a Philadelphia chromosome in chronic myelocytic leukaemia. Nature. 1983;306(5940):277-280.
  3. Heisterkamp N, Stephenson JR, Groffen J, et al. Localization of the c-ab1 oncogene adjacent to a translocation break point in chronic myelocytic leukaemia. Nature. 1983;306(5940):239-242.
  4. Khoury JD, Solary E, Abla O, et al. The 5th edition of the World Health Organization Classification of Haematolymphoid Tumours: Myeloid and Histiocytic/Dendritic Neoplasms. Leukemia. 2022;36(7):1703-1719.
  5. Hukku S, Baboo HA, Venkataratnam S, Vidyasagar MS, Patel NL. Splenic irradiation in chronic myeloid leukemia. Acta Radiol Oncol. 1983;22(1):9-12.
  6. Morstyn G, Sullivan J, Fairhead S, Cowling D, Hurley T. Effects of high dose busulphan on leukaemic progenitor cells in chronic myeloid leukaemia. Aust N Z J Med. 1981;11(6):609-614.
  7. Kennedy BJ. Hydroxyurea therapy in chronic myelogenous leukemia. Cancer. 1972;29(4):1052-1056.
  8. Talpaz M, McCredie K, Kantarjian H, Trujillo J, Keating M, Gutterman J. Chronic myelogenous leukaemia: haematological remissions with alpha interferon. Br J Haematol. 1986;64(1):87-95.

Details

Primary Language

English

Subjects

Haematological Tumours

Journal Section

Research Article

Publication Date

September 8, 2025

Submission Date

February 12, 2025

Acceptance Date

April 25, 2025

Published in Issue

Year 2025 Volume: 64 Number: 3

Vancouver
1.Ümit Çavdar, Fatma Keklik Karadağ, Fahri Şahin, Güray Saydam. A retrospective evaluation of chronic myeloid leukemia patients treated with imatinib. EJM. 2025 Sep. 1;64(3):438-43. doi:10.19161/etd.1636000

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