Literature DB >> 3625262

Policies for study monitoring and interim reporting of results.

S J Green, T R Fleming, J R O'Fallon.   

Abstract

Interim analyses of comparative trials are necessary in order to monitor for extreme therapeutic results. However, closing studies and reporting results whenever "trends" appear increases the probability of a false conclusion to well over the desired .05 level. Guidelines for early stopping of comparative trials must be carefully defined to avoid this problem. In addition, to avoid inappropriate early closure of studies due to declining accrual (as investigators draw their own conclusions from early unreliable data), it is recommended that access to interim data be limited to a multidisciplinary monitoring committee responsible for (1) performing and reviewing interim analyses, and (2) deciding when early termination should be considered. Accrual and reporting of studies from two clinical trials groups, one with a policy of limited access to interim data and one without, are compared. The group without monitoring committees had a higher incidence of accrual and reporting problems than the group with monitoring committees.

Mesh:

Year:  1987        PMID: 3625262     DOI: 10.1200/JCO.1987.5.9.1477

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  6 in total

Review 1.  Trials and fast changing technologies: the case for tracker studies.

Authors:  R J Lilford; D A Braunholtz; R Greenhalgh; S J Edwards
Journal:  BMJ       Date:  2000-01-01

Review 2.  Monitoring clinical trials--interim data should be publicly available.

Authors:  R J Lilford; D Braunholtz; S Edwards; A Stevens
Journal:  BMJ       Date:  2001-08-25

3.  Data Monitoring Committees: Current issues.

Authors:  Thomas R Fleming; Susan S Ellenberg; David L DeMets
Journal:  Clin Trials       Date:  2018-04-09       Impact factor: 2.486

4.  Protecting the confidentiality of interim data: addressing current challenges.

Authors:  Thomas R Fleming
Journal:  Clin Trials       Date:  2014-12-04       Impact factor: 2.486

5.  Maintaining confidentiality of interim data to enhance trial integrity and credibility.

Authors:  Thomas R Fleming; Katrina Sharples; John McCall; Andrew Moore; Anthony Rodgers; Ralph Stewart
Journal:  Clin Trials       Date:  2008       Impact factor: 2.486

6.  The effects of releasing early results from ongoing clinical trials.

Authors:  Steffen Ventz; Sergio Bacallado; Rifaquat Rahman; Sara Tolaney; Jonathan D Schoenfeld; Brian M Alexander; Lorenzo Trippa
Journal:  Nat Commun       Date:  2021-02-05       Impact factor: 14.919

  6 in total

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