CML in blast phase can occur de novo or can evolve while on treatment with a tyrosine kinase inhibitor. The blasts can be of myeloid or lymphoid lineage. It carries a poor prognosis and the aim of treatment is to induce remission/chronic phase, followed by consolidation with allogeneic haematopoietic cell transplantation.

Peripheral blood film from a patient with chronic myeloid leukaemia in blast phase (CML-BP). The patient presented with leukocytosis, splenomegaly and was found to have 34% blasts in the bone marrow. Cytogenetics revealed a t(9;22) translocation with added cytogenetic abnormalities. Note the frequent myeloblasts (in contrast to their rarity in CML-CP), abundance of mature neutrophils and myelocytes (including eosinophilic myelocytes) in the background.

Diagnostic Criteria (WHO 2016)

  • ≥20% blasts in the blood or bone marrow or
  • Presence of an extramedullary proliferation of blasts
  • Presence of the t(9;22) translocation or BCR/ABL fusion gene
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Peripheral blood film of a patient with CML in blast phase. Note the marked granulocytosis. There is a significant myeloblast population.

Blood Film Features:

  • Marked leucocytosis involving various stages of granulocytic maturation
  • Blast ≥ 20% blasts: may be of myeloid or lymphoid lineage
    • Myeloid lineage blast: may include neutrophilic, monocytic, megakaryocytic, basophilic, eosinophilic, or erythroid blasts
    • Lymphoid blast
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Bone marrow aspirate of a patient with CML in blast phase.

Bone Marrow Features:

  • Bone marrow is markedly hypercellular
  • Blast ≥ 20% blasts: may be of myeloid or lymphoid lineage

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