Grant: Discovery Grants Program - Individual
Memorial University of Newfoundland
$18,000.00
Statistical Modelling for Adaptive Design of Clinical Trials: Optimality and Efficiency
FY 2018-19
Summary
Response adaptive design (RAD) has ethical advantages over traditional methods for clinical trials, but it also introduces dependency into data. Most statistical literature on RAD focused on statistical methodologies for mean response models without considering population heterogeneity. Ignoring such heterogeneity could introduce bias into conclusions. In addition, patients exposed to different environmental factors may respond to treatments very differently. All these are the main reasons why the efficacious treatments recommended by randomized clinical trials do not always work in day-to-day health care.*This proposed research will develop new RAD to advocate the ethical advantages of RAD, propose statistical methods to account for the dependency introduced by RAD for various population heterogeneities, and establish efficient inferential methods for the proposed designs. This research will investigate the influence of adaptive randomization on statistical estimation, and employ that influence to improve the efficiency in learning on treatment effect. The population heterogeneities considered in this research include patients' and institutional characteristics and their interactions with treatments as well as patients' responses to a series of treatments.*This research will establish statistical methods for RAD with covariates and interaction, especially qualitative interaction, as well as for RAD for dynamic treatment region clinical trials. The results will add to the statistical literature on estimation for dependent data under adaptive randomization as well as optimal designs of clinical trials for heterogeneous populations. The use of RAD to adaptively learn on qualitative interaction may improve the efficiency of detecting subpopulations. Statistical methods developed for clustered responses will add efficient ethical designs for multi-center trials. The integration of adaptive randomization into clinical trials of dynamic treatment region (DTR) will enable adaptive learning on the optimal DTR thus improving the ethical benefit and statistical efficiency.*This proposed research addresses the methodological challenges in design and analysis of clinical trials when facing population heterogeneities. The developed methodologies incorporate population heterogeneities in RAD learning to advocate the ethical benefits and to improve statistical power. This research will add innovative designs of clinical trials and efficient statistical methods to statistical literature. The resulting toolbox can be generalized to other clinical settings where practitioners hope to efficiently identify optimal treatments for subpopulations.*
Program
Discovery Grants Program - Individual
Recipient
Location
Newfoundland and Labrador, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data
As published
Application id
RGPIN-2016-05221
Name nom
Yi, Yanqing
Department département
Medicine, Faculty of
Organization id
89
Institution établissement
Memorial University of Newfoundland
Province en
Newfoundland and Labrador
Province fr
Terre-Neuve-et-Labrador
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2018
Competition year année de concours
2016
Award amount
18000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
1508
Committee name en
Mathematics and Statistics
Committee name fr
Mathématiques et statistique
Area of application code
1211
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Medical and health sciences
Area of application fr
Sciences médicales et de la santé
Research subject code
3005
Research subject group en
Statistics and probability
Research subject group fr
Statistique et probabilité
Research subject en
Biostatistics
Research subject fr
Biostatistiques
Partie
3
Nb partie
5
Application title
Statistical Modelling for Adaptive Design of Clinical Trials: Optimality and Efficiency
Keyword
NSERC
Application summary
Response adaptive design (RAD) has ethical advantages over traditional methods for clinical trials, but it also introduces dependency into data. Most statistical literature on RAD focused on statistical methodologies for mean response models without considering population heterogeneity. Ignoring such heterogeneity could introduce bias into conclusions. In addition, patients exposed to different environmental factors may respond to treatments very differently. All these are the main reasons why the efficacious treatments recommended by randomized clinical trials do not always work in day-to-day health care.*This proposed research will develop new RAD to advocate the ethical advantages of RAD, propose statistical methods to account for the dependency introduced by RAD for various population heterogeneities, and establish efficient inferential methods for the proposed designs. This research will investigate the influence of adaptive randomization on statistical estimation, and employ that influence to improve the efficiency in learning on treatment effect. The population heterogeneities considered in this research include patients' and institutional characteristics and their interactions with treatments as well as patients' responses to a series of treatments.*This research will establish statistical methods for RAD with covariates and interaction, especially qualitative interaction, as well as for RAD for dynamic treatment region clinical trials. The results will add to the statistical literature on estimation for dependent data under adaptive randomization as well as optimal designs of clinical trials for heterogeneous populations. The use of RAD to adaptively learn on qualitative interaction may improve the efficiency of detecting subpopulations. Statistical methods developed for clustered responses will add efficient ethical designs for multi-center trials. The integration of adaptive randomization into clinical trials of dynamic treatment region (DTR) will enable adaptive learning on the optimal DTR thus improving the ethical benefit and statistical efficiency.*This proposed research addresses the methodological challenges in design and analysis of clinical trials when facing population heterogeneities. The developed methodologies incorporate population heterogeneities in RAD learning to advocate the ethical benefits and to improve statistical power. This research will add innovative designs of clinical trials and efficient statistical methods to statistical literature. The resulting toolbox can be generalized to other clinical settings where practitioners hope to efficiently identify optimal treatments for subpopulations.*