Literature DB >> 20888929

Phase II cancer clinical trials with a one-sample log-rank test and its corrections based on the Edgeworth expansion.

Xiaoqun Sun1, Paul Peng, Dongsheng Tu.   

Abstract

The response rate has been frequently used as the primary endpoint of phase II cancer clinical trials. It may not be an appropriate endpoint when a new treatment is not expected to produce any tumour shrinkage. When a large database for a historical control is available, the direct comparison of survival curves between a new treatment and the historical control may be made in phase II cancer clinical trials. In this paper, a one-sample log-rank test is introduced for the design and analysis of phase II cancer clinical trials with time-to-event endpoints. Corrections to the one-sample log-rank test are also derived based on the Edgeworth expansion. Simulations showed that the original one-sample log-rank test may be preferred if strictly controlling for type I error is important or when the sample size of a phase II trial is as large as 50, and a corrected one-sample log-rank test is used if the sample size of a phase II trial is small. A data set from a clinical trial conducted by the NCIC Clinical Trials Group is used to illustrate the proposed procedures.
Copyright © 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20888929     DOI: 10.1016/j.cct.2010.09.009

Source DB:  PubMed          Journal:  Contemp Clin Trials        ISSN: 1551-7144            Impact factor:   2.226


  10 in total

1.  Single-arm Phase II cancer survival trial designs.

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Journal:  J Biopharm Stat       Date:  2015-06-22       Impact factor: 1.051

2.  Two-stage optimal designs based on exact variance for a single-arm trial with survival endpoints.

Authors:  Guogen Shan
Journal:  J Biopharm Stat       Date:  2020-03-04       Impact factor: 1.051

3.  Single-Arm Phase II Survival Trial Design Under the Proportional Hazards Model.

Authors:  Jianrong Wu
Journal:  Stat Biopharm Res       Date:  2017-03-02       Impact factor: 1.452

4.  Obinutuzumab and idelalisib in symptomatic patients with relapsed/refractory Waldenström macroglobulinemia.

Authors:  Cécile Tomowiak; Stéphanie Poulain; Charles Herbaux; Aurore Perrot; Béatrice Mahé; Pierre Morel; Thérèse Aurran; Olivier Tournilhac; Stéphane Leprêtre; Souad Assaad; Bruno Villemagne; Olivier Casasnovas; Delphine Nollet; Damien Roos-Weil; Sylvie Chevret; Véronique Leblond
Journal:  Blood Adv       Date:  2021-05-11

5.  Two-stage phase II survival trial design.

Authors:  Jianrong Wu; Li Chen; Jing Wei; Heidi Weiss; Aman Chauhan
Journal:  Pharm Stat       Date:  2019-11-21       Impact factor: 1.234

6.  Sample size calculation for small sample single-arm trials for time-to-event data: Logrank test with normal approximation or test statistic based on exact chi-square distribution?

Authors:  Milind A Phadnis
Journal:  Contemp Clin Trials Commun       Date:  2019-04-13

7.  Optimal two-stage design of single arm Phase II clinical trials based on median event time test.

Authors:  Yeonhee Park
Journal:  PLoS One       Date:  2021-02-08       Impact factor: 3.240

8.  Reference curve sampling variability in one-sample log-rank tests.

Authors:  Moritz Fabian Danzer; Jannik Feld; Andreas Faldum; Rene Schmidt
Journal:  PLoS One       Date:  2022-07-21       Impact factor: 3.752

9.  A two-stage design for phase II trials with time-to-event endpoint using restricted follow-up.

Authors:  Lisa Belin; Yann De Rycke; Philippe Broët
Journal:  Contemp Clin Trials Commun       Date:  2017-10-01

10.  Assessing accuracy of Weibull shape parameter estimate from historical studies for subsequent sample size calculation in clinical trials with time-to-event outcome.

Authors:  Milind A Phadnis; Palash Sharma; Nadeesha Thewarapperuma; Prabhakar Chalise
Journal:  Contemp Clin Trials Commun       Date:  2020-02-26
  10 in total

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