Literature DB >> 33042476

Interim Monitoring for Futility in Clinical Trials with Two Co-primary Endpoints Using Prediction.

Koko Asakura1,2, Scott R Evans3, Toshimitsu Hamasaki2,3.   

Abstract

We discuss using prediction as a flexible and practical approach for monitoring futility in clinical trials with two co-primary endpoints. This approach is appealing in that it provides quantitative evaluation of potential effect sizes and associated precision, and can be combined with flexible error-spending strategies. We extend prediction of effect size estimates and the construction of predicted intervals to the two co-primary endpoints case, and illustrate interim futility monitoring of treatment effects using prediction with an example. We also discuss alternative approaches based on the conditional and predictive powers, compare these methods and provide some guidance on the use of prediction for better decision in clinical trials with co-primary endpoints.

Entities:  

Keywords:  Conditional Power; Group-sequential designs; Interim analyses; Predicted intervals; Predictive Power; Type I error

Year:  2019        PMID: 33042476      PMCID: PMC7539647          DOI: 10.1080/19466315.2019.1677494

Source DB:  PubMed          Journal:  Stat Biopharm Res        ISSN: 1946-6315            Impact factor:   1.452


  24 in total

1.  Issues in designing flexible trials.

Authors:  Martin Posch; Peter Bauer; Werner Brannath
Journal:  Stat Med       Date:  2003-03-30       Impact factor: 2.373

2.  Does Treatment of Impaired Glucose Tolerance Improve Cardiovascular Outcomes in Patients with Previous Myocardial Infarction?

Authors:  Masanori Asakura; Jiyoong Kim; Hiroshi Asanuma; Toshimitsu Hamasaki; Kengo Tsukahara; Yorihiko Higashino; Tetsuya Ishikawa; Yasuharu Nakama; Shinji Koba; Yasuyuki Maruyama; Mitsuru Tsujimoto; Hideo Himeno; Takanori Ohkusa; Susumu Fujino; Makoto Shimizu; Tsutomu Endo; Shunichi Yoda; Takahiro Muroya; Toyoaki Murohara; Nobuyuki Ohte; Hiroshi Suzuki; Tohru Kohno; Kazuki Fukui; Takaaki Shiono; Hiroyuki Takase; Hiroyasu Uzui; Yoshiyuki Nagai; Yuji Hashimoto; Shuntaro Ikeda; Sumio Mizuno; Koichi Tamita; Masashi Fujita; Kazuo Satake; Yoshihiko Kinoshita; Tatsuya Nunohiro; Satoru Sakagami; Jitsuo Higaki; Isao Morii; Reimin Sawada; Yoshikazu Hiasa; Tomohiko Shigemasa; Makoto Nakahama; Masataka Sata; Osamu Doi; Tetsuro Ueda; Takahisa Yamada; Takayoshi Yamanouchi; Hajime Yamaguchi; Yukiko Morita; Hideki Hayashi; Masafumi Kitakaze
Journal:  Cardiovasc Drugs Ther       Date:  2017-08       Impact factor: 3.727

3.  Bayesian predictive approach to interim monitoring in clinical trials.

Authors:  Alexei Dmitrienko; Ming-Dauh Wang
Journal:  Stat Med       Date:  2006-07-15       Impact factor: 2.373

Review 4.  Design, data monitoring, and analysis of clinical trials with co-primary endpoints: A review.

Authors:  Toshimitsu Hamasaki; Scott R Evans; Koko Asakura
Journal:  J Biopharm Stat       Date:  2017-10-30       Impact factor: 1.051

5.  A logrank test-based method for sizing clinical trials with two co-primary time-to-event endpoints.

Authors:  Tomoyuki Sugimoto; Takashi Sozu; Toshimitsu Hamasaki; Scott R Evans
Journal:  Biostatistics       Date:  2013-01-10       Impact factor: 5.899

6.  Sample size determination in group-sequential clinical trials with two co-primary endpoints.

Authors:  Koko Asakura; Toshimitsu Hamasaki; Tomoyuki Sugimoto; Kenichi Hayashi; Scott R Evans; Takashi Sozu
Journal:  Stat Med       Date:  2014-03-27       Impact factor: 2.373

7.  Alternative views on setting clinical trial futility criteria.

Authors:  Paul Gallo; Lu Mao; Vivian H Shih
Journal:  J Biopharm Stat       Date:  2014       Impact factor: 1.051

8.  Predictive probability early termination plans for phase II clinical trials.

Authors:  J Herson
Journal:  Biometrics       Date:  1979-12       Impact factor: 2.571

9.  Group-sequential logrank methods for trial designs using bivariate non-competing event-time outcomes.

Authors:  Tomoyuki Sugimoto; Toshimitsu Hamasaki; Scott R Evans; Susan Halabi
Journal:  Lifetime Data Anal       Date:  2019-04-12       Impact factor: 1.588

10.  Sizing clinical trials when comparing bivariate time-to-event outcomes.

Authors:  Tomoyuki Sugimoto; Toshimitsu Hamasaki; Scott R Evans; Takashi Sozu
Journal:  Stat Med       Date:  2017-01-24       Impact factor: 2.373

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  1 in total

Review 1.  Essential statistical principles of clinical trials of pain treatments.

Authors:  Robert H Dworkin; Scott R Evans; Omar Mbowe; Michael P McDermott
Journal:  Pain Rep       Date:  2020-12-18
  1 in total

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