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Statistical Methods for Survival Trial Design - Jianrong Wu

Statistical Methods for Survival Trial Design

With Applications to Cancer Clinical Trials Using R

(Autor)

Buch | Softcover
257 Seiten
2020
Chapman & Hall/CRC (Verlag)
978-0-367-73432-9 (ISBN)
CHF 79,95 inkl. MwSt
This book focuses on clinical trial design and monitoring with time-to-event endpoints. Detail of subjects of the book are included in book contents. This book not only provides a comprehensive review of existing methods. The book also presents a general group sequential method for trial monitoring which has not been published in any book.
Statistical Methods for Survival Trial Design: With Applications to Cancer Clinical Trials Using R provides a thorough presentation of the principles of designing and monitoring cancer clinical trials in which time-to-event is the primary endpoint. Traditional cancer trial designs with time-to-event endpoints are often limited to the exponential model or proportional hazards model. In practice, however, those model assumptions may not be satisfied for long-term survival trials.



This book is the first to cover comprehensively the many newly developed methodologies for survival trial design, including trial design under the Weibull survival models; extensions of the sample size calculations under the proportional hazard models; and trial design under mixture cure models, complex survival models, Cox regression models, and competing-risk models. A general sequential procedure based on the sequential conditional probability ratio test is also implemented for survival trial monitoring. All methodologies are presented with sufficient detail for interested researchers or graduate students.

Jianrong (John) Wu is a professor in the Division of Cancer Biostatistics, Department of Biostatistics, Markey Cancer Center, University of Kentucky. He has more than 15 years’ experience of designing and conducting cancer clinical trials at St. Jude Children’s Research Hospital and has developed several novel statistical methods for designing phase II and phase III survival trials.

Preface List of Figures List of Tables 1. Introduction to Cancer Clinical Trials General Aspects of Cancer Clinical Trial Design Study Objectives Treatment Plan Eligibility Criteria Statistical Considerations Statistical Aspects of Cancer Survival Trial Design Randomization Stratification Blinding Sample Size Calculation 2. Survival Analysis Survival Distribution Exponential Distribution Weibull Distribution Gamma Distribution Gompertz Distribution Log-Normal Distribution Log-Logistic Distribution Survival Data Fitting the Parametric Survival Distribution Kaplan-Meier Estimates Median Survival Time Log-Rank Test Cox Regression Model 3. Counting Process and Martingale_ Basic Convergence Concepts Counting Process Definition Martingale Central Limit Theorem Counting Process Formulation of Censored Survival Data 4. Survival Trial Design Under the Parametric Model Introduction Weibull Model Test Statistic Distribution of the MLE test Sample Size Formula Sample Size Calculation Accrual Duration Calculation Example and R code 5. Survival Trial Design Under the Proportional Hazards Model Introduction Proportional Hazards Model Asymptotic Distribution of the Log-rank Test Schoenfeld Formula Rubinstein Formula Freedman Formula Comparison Sample Size Calculation Under Various Models Example Optimal Properties of the Log-Rank Test_ Optimal Sample Size Allocation Optimal Power Precise Formula

Erscheinungsdatum
Reihe/Serie Chapman & Hall/CRC Biostatistics Series
Sprache englisch
Maße 156 x 234 mm
Gewicht 453 g
Themenwelt Mathematik / Informatik Mathematik Statistik
Studium 2. Studienabschnitt (Klinik) Humangenetik
ISBN-10 0-367-73432-X / 036773432X
ISBN-13 978-0-367-73432-9 / 9780367734329
Zustand Neuware
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