Impact of dose intensity of ponatinib on selected adverse events: Multivariate analyses from a pooled population of clinical trial patients
David J Dorer, Ronalk K. Knickerbocker, Michele Baccarani, Jorge E. Cortes, Andreas Hochhaus, Moshe Talpaz, Frank G. Haluska
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Ponatinib dose intensity was shown to be associated with rates of adverse events.
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Pancreatitis, rash, and cardiac failure were most strongly associated with dose.
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Time-to-event analyses suggest a lag between changes in dose and event risk.