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. 2016 Aug 31;7:287. doi: 10.3389/fphar.2016.00287

Table 4.

Dose modification and/or interruption due to adverse events.

Dose reductions n, % 9 (23.7%)*
Treatment interruptions n, % 0

n, number of patients.

*

~45% of patients received a subsequent re-escalation of dose within 3 weeks.