Statistical Methods for Survival Trial Design: With Applications to Cancer Clinical Trials Using R: Chapman & Hall/CRC Biostatistics Series
Autor Jianrong Wuen Limba Engleză Paperback – 18 dec 2020
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.
Toate formatele și edițiile | Preț | Express |
---|---|---|
Paperback (1) | 310.65 lei 6-8 săpt. | |
CRC Press – 18 dec 2020 | 310.65 lei 6-8 săpt. | |
Hardback (1) | 623.05 lei 6-8 săpt. | |
CRC Press – 18 iun 2018 | 623.05 lei 6-8 săpt. |
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Specificații
ISBN-13: 9780367734329
ISBN-10: 036773432X
Pagini: 273
Dimensiuni: 156 x 234 mm
Greutate: 0.45 kg
Ediția:1
Editura: CRC Press
Colecția Chapman and Hall/CRC
Seria Chapman & Hall/CRC Biostatistics Series
ISBN-10: 036773432X
Pagini: 273
Dimensiuni: 156 x 234 mm
Greutate: 0.45 kg
Ediția:1
Editura: CRC Press
Colecția Chapman and Hall/CRC
Seria Chapman & Hall/CRC Biostatistics Series
Notă biografică
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.
Recenzii
". . . this book provides a comprehensive introduction to statistical methods in cancer of sample size calculations and survival clinical trial designs from the classical techniques to the newly proposed formulae such as the mixture cure model and a group sequential trial design. This book has a vast list of citations and is an excellent reference for statisticians performing oncology research in the pharmaceutical industry or in other settings, and for graduate students in biostatistics or in related fields." ~ Journal of Biopharmaceutical Statistics
"I would recommend this book for those that are starting to work with this kind of trial design and would like to have a good overview and source of knowledge
for some not so common methods for more complex cancer trial designs, including simple formulae to implement in R to calculate sample sizes."
~David Manteigas, ISCB Newsletter
"I would recommend this book for those that are starting to work with this kind of trial design and would like to have a good overview and source of knowledge
for some not so common methods for more complex cancer trial designs, including simple formulae to implement in R to calculate sample sizes."
~David Manteigas, ISCB Newsletter
Descriere
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.