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. 2021 Jan 5;26(4):e622–e631. doi: 10.1002/onco.13632

Figure 1.

Figure 1

Onset of all‐cause AEs before and after dose reduction in the safety population. Worst‐grade period is presented for the onset of any AE, cognitive effects, edemas, nausea, fatigue, anemia, and diarrhea in patients who experienced dose reduction (n = 81).Abbreviation: AE, adverse event.