Fig. 3From: A stratified adaptive two-stage design with co-primary endpoints for phase II clinical oncology trialsStratified Adaptive Bryant & Day (SABD) design. e: ‹‹enrichment››. + : ‹‹inclusion of additional››. N1− and N1+: number of patients to be included at the first stage. N2−, N2+ and N2e+: number of patients to be included at the second stage. N− = N1− + N2−, N+ = N1+ + N2+ and Ne+ = N1+ + N2e+: total number of patients to be included. kR1−, kT1−, kR1+ and kT1+: first stage stopping boundaries. kR−, kT−, kR+, kT+, kRe+ and kTe+: second stage stopping boundaries. XR1−, XT1−, XR1+ and XT1+: number of responses and non-toxicities observed during the first stage. XR2−, XT2− XR2+, XT2+, XR2e+ and XT2e+: number of responses and non-toxicities observed during the second stage. XR− = XR1− + XR2−, XT− = XT1− + XT2−, XR+ = XR1+ + XR2+, XT+ = XT1+ + XT2+, XRe+ = XR1+ + XR2e+ and XTe+ = XT1+ + XT2e+: total number of responses and non-toxicities observedBack to article page