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wanneer laboratoriumabnormaliteiten en bijwerkingen werden samengenomen voor de combinatie- en monotherapiebehandelingsfasen, werden graad 3 of graad 4 neutrofiele abnormaliteiten, waaronder neutropenie, waargenomen bij 8 % van de patiënten.
when laboratory abnormalities and adverse events were combined across concomitant and monotherapy treatment phases, grade 3 or grade 4 neutrophil abnormalities including neutropenic events were observed in 8 % of the patients.
Last Update: 2017-04-26
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