between crizotinib and chemotherapy among responders, owing to the higher objective response rate in the crizotinib arm, it would undermine the treatment benefit with respect to DOR. A caveat for our proposal is that mean DOR depends on a specific time window that can be preselected based on clinical consideration. Empirically one may choose the largest possible time window beyond which a small proportion of patients (eg, 2%) remain at risk for P/D. Like other procedures such as hazard ratio estimation, this time window constraint may not be avoidable without a parametric model for extrapolation. Lastly, it can be quite informative to exam-
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Childers et al. (2018) studied this question.
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