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. Author manuscript; available in PMC: 2024 Jun 1.
Published in final edited form as: Clin Trials. 2024 Apr 9;21(3):322–330. doi: 10.1177/17407745231221152

Table 2.

Simulations scenarios following the idelalisib example: cumulative incidence of DLT at the end of the observation window (Obs. window) by dose level (D1 to D5), and by length of window. Maximum tolerated dose is given in bold.

Cumulative incidence of DLT at the end of window

Obs. window Hazard D1 D2 D3 D4 D5

16 weeks Constant (100% of toxicity events in [0,16w]) 0.10 0.25 0.45 0.60 0.75
4 weeks Decreasing (78% of toxicity events in [0,4w]) 0.077 0.196 0.364 0.501 0.650
4 weeks Decreasing (59% of toxicity events in [0,4w]) 0.056 0.147 0.281 0.396 0.534
4 weeks Constant (25% of toxicity events in [0,4w]) 0.026 0.069 0.139 0.205 0.293