Methods and Applications of Sample Size Calculation and Recalculation in Clinical Trials
暫譯: 臨床試驗中樣本大小計算與重新計算的方法與應用

Kieser, Meinhard

  • 出版商: Springer
  • 出版日期: 2020-11-20
  • 售價: $4,000
  • 貴賓價: 9.5$3,800
  • 語言: 英文
  • 頁數: 396
  • 裝訂: Hardcover - also called cloth, retail trade, or trade
  • ISBN: 3030495272
  • ISBN-13: 9783030495275
  • 相關分類: Data Science機率統計學 Probability-and-statistics
  • 海外代購書籍(需單獨結帳)

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商品描述

This book provides an extensive overview of the principles and methods of sample size calculation and recalculation in clinical trials. Appropriate calculation of the required sample size is crucial for the success of clinical trials. At the same time, a sample size that is too small or too large is problematic due to ethical, scientific, and economic reasons. Therefore, state-of-the art methods are required when planning clinical trials.

Part I describes a general framework for deriving sample size calculation procedures. This enables an understanding of the common principles underlying the numerous methods presented in the following chapters. Part II addresses the fixed sample size design, where the required sample size is determined in the planning stage and is not changed afterwards. It covers sample size calculation methods for superiority, non-inferiority, and equivalence trials, as well as comparisons between two and more than two groups. A wide range of further topics is discussed, including sample size calculation for multiple comparisons, safety assessment, and multi-regional trials. There is often some uncertainty about the assumptions to be made when calculating the sample size upfront. Part III presents methods that allow to modify the initially specified sample size based on new information that becomes available during the ongoing trial. Blinded sample size recalculation procedures for internal pilot study designs are considered, as well as methods for sample size reassessment in adaptive designs that use unblinded data from interim analyses. The application is illustrated using numerous clinical trial examples, and software code implementing the methods is provided.

The book offers theoretical background and practical advice for biostatisticians and clinicians from the pharmaceutical industry and academia who are involved in clinical trials. Covering basic as well as more advanced and recently developed methods, it is suitable for beginners, experienced applied statisticians, and practitioners. To gain maximum benefit, readers should be familiar with introductory statistics. The content of this book has been successfully used for courses on the topic.


商品描述(中文翻譯)

本書提供了臨床試驗中樣本大小計算及重新計算原則和方法的廣泛概述。適當計算所需的樣本大小對臨床試驗的成功至關重要。同時,樣本大小過小或過大都會因為倫理、科學和經濟原因而成為問題。因此,在規劃臨床試驗時需要採用最先進的方法。

第一部分描述了一個通用框架,用於推導樣本大小計算程序。這使得讀者能夠理解後續章節中所呈現的眾多方法所基於的共同原則。第二部分針對固定樣本大小設計進行探討,在此設計中,所需的樣本大小在規劃階段確定,之後不再更改。它涵蓋了優越性、非劣性和等效性試驗的樣本大小計算方法,以及兩組和多於兩組之間的比較。還討論了多重比較的樣本大小計算、安全性評估和多區域試驗等廣泛主題。在提前計算樣本大小時,通常會對所需假設存在一些不確定性。第三部分介紹了根據在進行中的試驗中獲得的新信息來修改最初指定的樣本大小的方法。考慮了針對內部試點研究設計的盲法樣本大小重新計算程序,以及在使用來自中期分析的非盲數據的自適應設計中進行樣本大小重新評估的方法。應用部分通過眾多臨床試驗示例進行說明,並提供了實現這些方法的軟體代碼。

本書為參與臨床試驗的生物統計學家和來自製藥行業及學術界的臨床醫生提供了理論背景和實用建議。涵蓋了基本及更高級和最近開發的方法,適合初學者、經驗豐富的應用統計學家和實務工作者。為了獲得最大的收益,讀者應熟悉入門統計學。本書的內容已成功用於相關主題的課程。

作者簡介

Prof. Dr. Meinhard Kieser is a Professor of Medical Biometry and Director of the Institute of Medical Biometry and Informatics at the University of Heidelberg. He studied Mathematics and received his PhD in Medical Biometry in 1992. He then worked for more than 15 years as a biostatistician and Head of Biometrics in the pharmaceutical industry. Professor Kieser has comprehensive experience in the planning and analysis of clinical trials and has been a member of numerous independent data monitoring committees. He serves as an associate editor for Pharmaceutical Statistics and the Journal of Biopharmaceutical Statistics. His main research areas are biostatistical methods for clinical trials, including sample size calculation and recalculation, and methods for evidence synthesis.

作者簡介(中文翻譯)

梅因哈德·基澤教授(Prof. Dr. Meinhard Kieser)是海德堡大學醫學生物統計學教授及醫學生物統計與資訊學研究所所長。他主修數學,並於1992年獲得醫學生物統計學博士學位。隨後,他在製藥行業擔任生物統計師及生物統計部門負責人超過15年。基澤教授在臨床試驗的規劃和分析方面擁有豐富的經驗,並曾是多個獨立數據監測委員會的成員。他擔任《Pharmaceutical Statistics》和《Journal of Biopharmaceutical Statistics》的副編輯。他的主要研究領域包括臨床試驗的生物統計方法,涵蓋樣本大小計算及重新計算,以及證據綜合的方法。