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Fig. 3 | BMC Medical Research Methodology

Fig. 3

From: A stratified adaptive two-stage design with co-primary endpoints for phase II clinical oncology trials

Fig. 3

Stratified 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 observed

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