TY - JOUR
T1 - Urn models for response-adaptive randomized designs: a simulation study based on a non-adaptive randomized trial
AU - Ghiglietti, Andrea
AU - Scarale, M. G.
AU - Miceli, R.
AU - Ieva, F.
AU - Mariani, L.
AU - Gavazzi, C.
AU - Paganoni, A. M.
AU - Edefonti, V.
PY - 2018
Y1 - 2018
N2 - Recently, response-adaptive designs have been proposed in randomized clinical trials to achieve ethical and/or cost advantages by using sequential accrual information collected during the trial to dynamically update the probabilities of treatment assignments. In this context, urn models—where the probability to assign patients to treatments is interpreted as the proportion of balls of different colors available in a virtual urn—have been used as response-adaptive randomization rules.\r\nWe propose the use of Randomly Reinforced Urn (RRU) models in a simulation study based on a published randomized clinical trial on the efficacy of home enteral nutrition in cancer patients after major gastrointestinal surgery. We compare results with the RRU design with those previously published with the non-adaptive approach. We also provide a code written with the R software to implement the RRU design in practice.\r\n\r\nIn detail, we simulate 10,000 trials based on the RRU model in three set-ups of different total sample sizes. We report information on the number of patients allocated to the inferior treatment and on the empirical power of the t-test for the treatment coefficient in the ANOVA model. We carry out a sensitivity analysis to assess the effect of different urn compositions.\r\nFor each sample size, in approximately 75% of the simulation runs, the number of patients allocated to the inferior treatment by the RRU design is lower, as compared to the non-adaptive design. The empirical power of the t-test for the treatment effect is similar in the two designs.
AB - Recently, response-adaptive designs have been proposed in randomized clinical trials to achieve ethical and/or cost advantages by using sequential accrual information collected during the trial to dynamically update the probabilities of treatment assignments. In this context, urn models—where the probability to assign patients to treatments is interpreted as the proportion of balls of different colors available in a virtual urn—have been used as response-adaptive randomization rules.\r\nWe propose the use of Randomly Reinforced Urn (RRU) models in a simulation study based on a published randomized clinical trial on the efficacy of home enteral nutrition in cancer patients after major gastrointestinal surgery. We compare results with the RRU design with those previously published with the non-adaptive approach. We also provide a code written with the R software to implement the RRU design in practice.\r\n\r\nIn detail, we simulate 10,000 trials based on the RRU model in three set-ups of different total sample sizes. We report information on the number of patients allocated to the inferior treatment and on the empirical power of the t-test for the treatment coefficient in the ANOVA model. We carry out a sensitivity analysis to assess the effect of different urn compositions.\r\nFor each sample size, in approximately 75% of the simulation runs, the number of patients allocated to the inferior treatment by the RRU design is lower, as compared to the non-adaptive design. The empirical power of the t-test for the treatment effect is similar in the two designs.
KW - Non-adaptive trial design
KW - randomized trials
KW - randomly reinforced urn model
KW - response-adaptive randomization
KW - simulation study
KW - Non-adaptive trial design
KW - randomized trials
KW - randomly reinforced urn model
KW - response-adaptive randomization
KW - simulation study
UR - https://publicatt.unicatt.it/handle/10807/117575
UR - https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85044276889&origin=inward
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85044276889&origin=inward
U2 - 10.1080/10543406.2018.1452024
DO - 10.1080/10543406.2018.1452024
M3 - Article
SN - 1054-3406
SP - 1
EP - 14
JO - Journal of Biopharmaceutical Statistics
JF - Journal of Biopharmaceutical Statistics
IS - N/A
ER -