Chronic phase |
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High risk
Low risk
Blasts <10% in peripheral blood or bone marrow
Basophils <20% in peripheral blood or bone marrow
Clonal evolution present at diagnosis but does not progress during the course of therapy
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Accelerated phase |
Blasts 15%–29% in blood or bone marrow; blasts plus promyelocytes >30% in blood or bone marrow, with blasts <30%
Basophils ≥20% in blood
Persistent thrombocytopenia (<100 × 109/L) unrelated to therapy
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Blasts 10%–29% in peripheral blood or bone marrow
Blasts plus promyelocytes ≥30%
Basophils ≥20% in peripheral blood or bone marrow
Platelets <100 × 109/L unrelated to therapy
Persistent splenomegaly, white blood cell count > 10 × 109/L, or platelets > 1000 × 109/L unresponsive to sustained therapy
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Blasts 10%–19% of white blood cells in peripheral and/or nucleated bone marrow cells
Peripheral blood basophils ≥20%
Persistent thrombocytopenia (<100 × 109/L) unrelated to therapy or persistent thrombocytosis (≥1000 × 109/L) unresponsive to therapy
Increasing spleen size and increasing white blood cell count unresponsive to therapy
Cytogenetic evidence of clonal evolution
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Blast crisis |
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Blasts ≥20% of peripheral blood white cells or nucleated bone marrow cells
Extramedullary blast proliferation
Large foci or clusters of blasts in the bone marrow biopsy
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