Resumen de Chronic myeloid leukaemia
Katharine Hanlon, Mhairi Copland
Chronic myeloid leukaemia (CML) is a clonal myeloproliferative disorder resulting from a reciprocal translocation between the long arms of chromosomes 9 and 22. This is termed the Philadelphia chromosome, and leads to production of the fusion onco-protein BCR-ABL, a 210 kDa constitutively active tyrosine kinase. CML has three distinct phases: the chronic, accelerated and blast phases. Most patients (85%) present in the chronic phase, which is associated with leucocytosis and splenomegaly. More advanced phases are associated with bone marrow failure and carry a poor prognosis. The introduction of tyrosine kinase inhibitors (TKIs; imatinib, dasatinib, nilotinib, bosutinib, ponatinib) has altered the clinical course of CML for most patients, turning it from a fatal leukaemia to a chronic disorder managed with oral medication. Patients with chronic-phase CML have excellent levels of response to TKIs, and individuals with an optimal response can expect a normal lifespan. However, resistance to TKIs is seen, particularly in the advanced phases of CML. In these patients, allogeneic stem cell transplantation may warrant consideration. With increasing experience in the use of TKIs, different adverse effect profiles are emerging and require consideration when choosing the most suitable TKI for an individual patient.
