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Table 5 Summary of ibrutinib dose discontinuation rates or modification in clinical trials vs “real-world practice” studies

From: Ibrutinib dose modifications in the management of CLL

 

Clinical trial

Real-world

Average discontinuation rate due to toxicity

36.3% (range 13–64.7%)

45.2% (range 9.7–63.1%)

Average discontinuation rate due to relapsed disease

34.2% (range 11.8–50.5%)

25.5% (range 12.8–53%)

Average dose reduction over 1 year

7.3% (range 6–9%)

20.5% (range 11–31.3%)