Figure 1
Figure 1. Cumulative incidence of anemia, thrombocytopenia, and marked leukocytosis in PMF patients stratified according to their driver mutation. The thresholds for hemoglobin level and WBC count are those of the IPSS,3 whereas that for PLT count is the lower limit of normal range. Cumulative incidences were estimated with a competing risk approach, considering death for any cause as a competing event. Vertical tick marks indicate right-censored patients. (A) Cumulative incidence of anemia (hemoglobin <10 g/dL). CALR-mutant patients had a lower incidence of anemia compared with the remaining patients (maximum P value equal to .004). (B) Cumulative incidence of thrombocytopenia (PLT count <100 × 109/L). The cumulative incidence of thrombocytopenia was significantly lower in CALR-mutant patients compared with the remaining ones (P < .001 in all comparisons). (C) Cumulative incidence of marked leukocytosis (WBC count >25 × 109/L). The cumulative incidence of marked leukocytosis was significantly lower in CALR-mutant patients compared with JAK2-mutant (P = .004) or triple-negative patients (P < .001).

Cumulative incidence of anemia, thrombocytopenia, and marked leukocytosis in PMF patients stratified according to their driver mutation. The thresholds for hemoglobin level and WBC count are those of the IPSS, whereas that for PLT count is the lower limit of normal range. Cumulative incidences were estimated with a competing risk approach, considering death for any cause as a competing event. Vertical tick marks indicate right-censored patients. (A) Cumulative incidence of anemia (hemoglobin <10 g/dL). CALR-mutant patients had a lower incidence of anemia compared with the remaining patients (maximum P value equal to .004). (B) Cumulative incidence of thrombocytopenia (PLT count <100 × 109/L). The cumulative incidence of thrombocytopenia was significantly lower in CALR-mutant patients compared with the remaining ones (P < .001 in all comparisons). (C) Cumulative incidence of marked leukocytosis (WBC count >25 × 109/L). The cumulative incidence of marked leukocytosis was significantly lower in CALR-mutant patients compared with JAK2-mutant (P = .004) or triple-negative patients (P < .001).

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