报告时间:2024年7月30日(星期二)10:00-11:30
报告地点:翡翠科教楼B座1710
报告人:Yong Zang Associate Professor
工作单位:Indiana University School of Medicine
举办单位:3522vip浦京集团
报告简介:
In the early phase development of molecularly targeted agents (MTAs), it is common to expect that an MTA will be more effective for a specific biomarker subgroup, such as marker-positive patients. However, there may not be sufficient evidence to prove that the MTA is ineffective for the other subgroup, namely, marker-negative patients. Once it is established that marker-positive patients benefit from the treatment, it becomes clinically important to determine whether this benefit also extends to marker-negative patients. To address this practical issue in phase II clinical trials, we propose a series of adaptive biomarker-guided designs. These designs can be implemented with or without the inclusion of a randomized control treatment. The proposed designs initially evaluate the treatment effect in marker-positive patients and subsequently assess marker-negative patients if necessary. Multiple interim analyses are incorporated to allow early termination of the trial if the MTA is found to be either futile or superior. Simulation studies indicate that the proposed adaptive designs perform well and are ethically more favorable compared to commonly used designs.
报告人简介:
Dr. Yong Zang is the Indiana University School of Medicine Showalter Scholar Associate Professor. He also serves as the Co-Director of Clinical Research for the Biostatistics and Data Management Core, IU Simon Comprehensive Cancer Center. He received his Ph.D. degree from The University of Hong Kong and finished his Postdoctoral training in The University of Texas, MD Anderson Cancer Center. His research interests are clinical trial design and statistical genetics. He has published over seventy papers in peer-reviewed statistical, genetics and medical journals such as Biometrics, Biostatistics, JRSSC, American Journal of Human Genetics, Genome Research, Cancer Research and Clinical Cancer Research. His research is supported by National Institute of Health, Showalter Trust and Indiana CTSI.