Figure 1
Figure 1. Platelet aggregation induced by different agonists in patients with CML in chronic phase receiving therapy with different tyrosine kinase inhibitors. Dasatinib was more frequently associated with epinephrine-induced platelet aggregation defects compared with imatinib, nilotinib, and bosutinib (P < .001, one-way ANOVA) and with AA-induced platelet aggregation defects compared with nilotinib and bosutinib (P < .001, t test), but not with imatinib (P = .55, t test). Error bars represent SD.

Platelet aggregation induced by different agonists in patients with CML in chronic phase receiving therapy with different tyrosine kinase inhibitors. Dasatinib was more frequently associated with epinephrine-induced platelet aggregation defects compared with imatinib, nilotinib, and bosutinib (P < .001, one-way ANOVA) and with AA-induced platelet aggregation defects compared with nilotinib and bosutinib (P < .001, t test), but not with imatinib (P = .55, t test). Error bars represent SD.

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