Table 2

Distribution of MPL mutations according to diagnosis in the Pavia and Florence merged cohorts

DiagnosisW515L*W515KW515AW515RW515SS505N
Essential thrombocythemia 22 (55%) 7 (17.5%) 6 (15%) 2 (5%) 2 (5%) 1 (2.5%) 
Primary myelofibrosis 13 (92.9%) 1 (7.1%) 
Post-essential thrombocythemia myelofibrosis 4 (50%) 3 (37.5%) 1 (12.5%) 
DiagnosisW515L*W515KW515AW515RW515SS505N
Essential thrombocythemia 22 (55%) 7 (17.5%) 6 (15%) 2 (5%) 2 (5%) 1 (2.5%) 
Primary myelofibrosis 13 (92.9%) 1 (7.1%) 
Post-essential thrombocythemia myelofibrosis 4 (50%) 3 (37.5%) 1 (12.5%) 
*

Two patients had another concomitant MPL mutation (S505C, V501A).

Two patients had another concomitant MPL mutation (V501A, Q516E).

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