JSM 2011 Online Program

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Activity Details

70 * Sun, 7/31/2011, 4:00 PM - 5:50 PM CC-D236
Topics in Oncology Studies — Contributed Papers
Biopharmaceutical Section
Organizer(s): Ying Lu, Palo Alto VA CSP Coordinating Center/Stanford
Chair(s): John Boscardin, San Francisco VA/University of California at San Francisco
4:05 PM Escalation with Overdose Control Using Normalized Equivalent Toxicity Score and Patient's Characteristics to Define Personalized Maximum Tolerated Dose in Phase I Clinical Trial Zhengjia Chen, Emory University ; Mourad Tighiouart, Emory University ; Yuan Liu, Emory University ; Zhibo Wang, Georgia State University ; Taofeek K. Owonikoko, Emory University ; Jeanne Kowalski, Emory University
4:20 PM A Comparison of Longitudinal and Time-to-Endpoint Approaches for Treatment Comparisons in Tumor Growth Studies Kingshuk Roy Choudhury, University College Cork ; Ian Kasman, Genentech Inc. ; Greg D. Plowman, Genentech Inc.
4:35 PM Exact Group Sequential Designs for Phase I Oncology Trials Karen Messer, Moores UCSD Cancer Center
4:50 PM Predicting Data Cutoff Dates for Event-Driven Randomized Survival Clinical Trials Before and During Study Conduct Ying Tian, Amgen Inc. ; Alan Rong, Amgen Inc. ; Alicia Zhang, Amgen Inc. ; Hua Yu, Amgen Inc.
5:05 PM Escalation with Overdose Control using Time to Toxicity Data for Cancer Phase I Clinical Trials Yuan Liu, Emory University ; Mourad Tighiouart, Emory University ; André Rogatko, Samuel Oschin Comprehensive Cancer Institute
5:20 PM Using Bayesian Proof-of-Concept (POC) Criteria to Design Randomized Phase II Oncology Trials Stratified by Biomarker Status — Kalyanee Appanna, Novartis Oncology ; Valentine Jehl, Novartis Oncology ; Yong Zhang, Novartis Oncology ; Yun Wang, Novartis Oncology ; Amy Racine, Novartis ; Beat Neuenschwander, Novartis Pharma AG ; Emmanuel Zuber, Novartis Oncology

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