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. Author manuscript; available in PMC: 2015 Mar 17.
Published in final edited form as: Clin Trials. 2013 Oct 1;10(6):862–875. doi: 10.1177/1740774513503521

Table 5.

Compared proportions of MTD recommendation and accuracy measure for the optimal design and CRM-L after 10,000 simulated trials. The true MTD is indicated in bold type. The target toxicity rate is 20% and the fixed sample size for each trial is 30 patients. First stage cohort size is 1.

Dose 1 2 3 4 5 6 7 8 A(n)
Scenario 13 0.09 0.20 0.26 0.44 0.58 0.74 0.83 0.90

CRM-L (A) 0.19 0.49 0.28 0.04 0.00 0.00 0.00 0.00 0.858
CRM-L (B) 0.21 0.46 0.29 0.04 0.00 0.00 0.00 0.00 0.848
Optimal 0.14 0.48 0.35 0.03 0.00 0.00 0.00 0.00 0.868

Scenario 14 0.05 0.10 0.20 0.30 0.45 0.58 0.70 0.81

CRM-L (A) 0.02 0.23 0.49 0.24 0.02 0.00 0.00 0.00 0.788
CRM-L (B) 0.02 0.23 0.48 0.24 0.02 0.00 0.00 0.00 0.784
Optimal 0.01 0.15 0.55 0.28 0.01 0.00 0.00 0.00 0.818

Scenario 15 0.02 0.05 0.11 0.20 0.33 0.48 0.60 0.72

CRM-L (A) 0.00 0.03 0.25 0.51 0.20 0.01 0.00 0.00 0.744
CRM-L (B) 0.00 0.03 0.25 0.51 0.20 0.01 0.00 0.00 0.742
Optimal 0.00 0.01 0.19 0.58 0.22 0.01 0.00 0.00 0.778

Scenario 16 0.01 0.04 0.07 0.10 0.18 0.31 0.50 0.64

CRM-L (A) 0.00 0.00 0.04 0.20 0.49 0.26 0.02 0.00 0.627
CRM-L (B) 0.00 0.00 0.03 0.20 0.50 0.24 0.02 0.0 0.625
Optimal 0.00 0.00 0.02 0.11 0.55 0.31 0.01 0.00 0.664

Scenario 17 0.01 0.02 0.04 0.06 0.08 0.13 0.20 0.36

CRM-L (A) 0.00 0.00 0.01 0.03 0.09 0.26 0.46 0.15 0.546
CRM-L (B) 0.00 0.00 0.00 0.02 0.09 0.28 0.44 0.17 0.526
Optimal 0.00 0.00 0.00 0.01 0.04 0.22 0.58 0.17 0.635

Scenario 18 0.01 0.03 0.05 0.07 0.09 0.11 0.14 0.20

CRM-L (A) 0.00 0.00 0.01 0.04 0.08 0.13 0.25 0.48 0.619
CRM-L (B) 0.00 0.00 0.01 0.03 0.07 0.12 0.23 0.53 0.654
Optimal 0.00 0.00 0.00 0.01 0.03 0.08 0.21 0.66 0.769

Avg. A(n): CRM-L (A) = 0.697; CRM-L(B) = 0.696; Optimal = 0.755