Literature DB >> 22162583

Consistency in the analysis and reporting of primary end points in oncology randomized controlled trials from registration to publication: a systematic review.

Benoit You1, Hui K Gan, Gregory Pond, Eric X Chen.   

Abstract

PURPOSE: To improve the quality of reporting of randomized clinical trials (RCTs), international registries for RCTs and guidelines for primary end point (PEP) analysis were established. The objectives of this systematic review were to evaluate concordance of PEP between publication and the corresponding registry and to assess intrapublication consistency in PEP reporting.
METHODS: All adult oncology RCTs in solid tumors published in 10 journals between 2005 and 2009 were reviewed. Registration information was extracted from international trial registries.
RESULTS: A total 366 RCTs were identified. Trial registration was found for 215 trials, and the rate increased from 43% in 2005 to 82% in 2009 (P < .001). There were 134 RCTs with clearly defined PEPs in registry, with the rate increasing from 15% to 67% (P < .001). PEP differed between registration and final publication in 14% trials with clearly defined PEPs. Reporting issues in methodology were found in 15% of RCTs, mainly because of inadequate reporting of PEP or sample size calculation. Problems with the interpretation of trial results were found in 22% publications, mostly resulting from negative superiority studies being interpreted as showing equivalence.
CONCLUSION: The rates of trial registration and of trials with clearly defined PEPs have improved over time; however, 14% of these trials reported a different PEP in the final publication. Intrapublication inconsistencies in PEP reporting are frequent. Our findings highlight the need for investigators, peer reviewers, and readers to exercise increased awareness and scrutiny of reporting outcomes of oncology RCTs.

Entities:  

Mesh:

Year:  2011        PMID: 22162583     DOI: 10.1200/JCO.2011.37.0890

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


  34 in total

Review 1.  Randomized controlled trials and neuro-oncology: should alternative designs be considered?

Authors:  Alireza Mansouri; Samuel Shin; Benjamin Cooper; Archita Srivastava; Mohit Bhandari; Douglas Kondziolka
Journal:  J Neurooncol       Date:  2015-08-22       Impact factor: 4.130

2.  SPIRIT 2013 explanation and elaboration: guidance for protocols of clinical trials.

Authors:  An-Wen Chan; Jennifer M Tetzlaff; Peter C Gøtzsche; Douglas G Altman; Howard Mann; Jesse A Berlin; Kay Dickersin; Asbjørn Hróbjartsson; Kenneth F Schulz; Wendy R Parulekar; Karmela Krleza-Jeric; Andreas Laupacis; David Moher
Journal:  BMJ       Date:  2013-01-08

3.  Trends in endpoint selection in clinical trials of advanced breast cancer.

Authors:  Seung Yeon Song; Heenam Seo; Gyungjin Kim; Ah Rong Kim; Eun Young Kim
Journal:  J Cancer Res Clin Oncol       Date:  2016-09-01       Impact factor: 4.553

4.  Meta-Research on Oncology Trials: A Toolkit for Researchers with Limited Resources.

Authors:  Rachel P Riechelmann; Julien Péron; Bostjan Seruga; Everardo D Saad
Journal:  Oncologist       Date:  2018-05-16

5.  Comparison of protocols and registry entries to published reports for randomised controlled trials.

Authors:  Kerry Dwan; Douglas G Altman; Lynne Cresswell; Michaela Blundell; Carrol L Gamble; Paula R Williamson
Journal:  Cochrane Database Syst Rev       Date:  2011-01-19

6.  Comparisons between protocols and publications of case-control studies: analysis of potential causes of non-reproducibility and recommendations for enhancing the quality of personalization in healthcare.

Authors:  Haifeng Hou; Guoyong Ding; Xuan Zhao; Zixiu Meng; Jiangmin Xu; Zheng Guo; Yulu Zheng; Dong Li; Wei Wang
Journal:  EPMA J       Date:  2019-03-19       Impact factor: 6.543

7.  Using ClinicalTrials.gov to supplement information in ophthalmology conference abstracts about trial outcomes: a comparison study.

Authors:  Roberta W Scherer; Lynn Huynh; Ann-Margret Ervin; Kay Dickersin
Journal:  PLoS One       Date:  2015-06-24       Impact factor: 3.240

Review 8.  Inadequate use and regulation of interventions against publication bias decreases their effectiveness: a systematic review.

Authors:  Kylie Thaler; Christina Kien; Barbara Nussbaumer; Megan G Van Noord; Ursula Griebler; Irma Klerings; Gerald Gartlehner
Journal:  J Clin Epidemiol       Date:  2015-01-30       Impact factor: 6.437

9.  ClinicalTrials.gov registration can supplement information in abstracts for systematic reviews: a comparison study.

Authors:  Roberta W Scherer; Lynn Huynh; Ann-Margret Ervin; Jakeisha Taylor; Kay Dickersin
Journal:  BMC Med Res Methodol       Date:  2013-06-18       Impact factor: 4.615

10.  The quality of registration of clinical trials: still a problem.

Authors:  Roderik F Viergever; Ghassan Karam; Andreas Reis; Davina Ghersi
Journal:  PLoS One       Date:  2014-01-10       Impact factor: 3.240

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