Monitoring response and resistance to treatment in chronic myeloid leukemia

  • S. Assouline McGill University
  • J. H. Lipton Princess Margaret Hospital


Chronic myeloid leukemia (CML) results from expression of the constitutive tyrosine kinase activity of the Bcr-Abl oncoprotein. Imatinib, a tyrosine kinase inhibitor (TKI), is highly effective in the treatment of CML. However, some patients treated with imatinib will fail to respond, will respond suboptimally, or will relapse because of primary or acquired resistance or intolerance. Research activities focusing on the mechanisms that underlie imatinib resistance have identified mutations in the BCR-ABL gene, clonal evolution, and amplification of the BCR-ABL gene as common causes. Cytogenetic and molecular techniques are currently used to monitor cml therapy for both response and relapse. With multiple and more potent therapeutic options now available, monitoring techniques can permit treatment to be tailored to the individual patient based on disease characteristics—for example, according to BCR-ABL mutation profile or to patient characteristics such as certain comorbid conditions. This approach should benefit patients by increasing the potential for better long-term outcomes.

Author Biographies

S. Assouline, McGill University

Department of Medicine and Oncology

McGill University

Jewish General Hospital

J. H. Lipton, Princess Margaret Hospital
Department of Medical Oncology and Hematology Princess Margaret Hospital University of Toronto
How to Cite
Assouline, S., & Lipton, J. H. (1). Monitoring response and resistance to treatment in chronic myeloid leukemia. Current Oncology, 18(2), e71-e83.