Literature DB >> 23824468

Monitoring in clinical trials: benefit or bias?

Cecilia Nardini1.   

Abstract

Monitoring ongoing clinical trials for early signs of effectiveness is an option for improving cost-effectiveness of trials that is becoming increasingly common. Alongside the obvious advantages made possible by monitoring, however, there are some downsides. In particular, there is growing concern in the medical community that trials stopped early for benefit tend to overestimate treatment effect. In this paper, I examine this problem from the point of view of statistical methodology, starting from the observation that the overestimation is caused by the statistical method adopted. Consequently, I argue that some modifications can and should be made to the present statistical framework in order not to miss the advantages the possibility of monitoring can grant.

Mesh:

Year:  2013        PMID: 23824468     DOI: 10.1007/s11017-013-9264-2

Source DB:  PubMed          Journal:  Theor Med Bioeth        ISSN: 1386-7415


  27 in total

1.  Ethics and practice: alternative designs for phase III randomized clinical trials.

Authors:  C R Palmer; W F Rosenberger
Journal:  Control Clin Trials       Date:  1999-04

Review 2.  Stopping randomized trials early for benefit and estimation of treatment effects: systematic review and meta-regression analysis.

Authors:  Dirk Bassler; Matthias Briel; Victor M Montori; Melanie Lane; Paul Glasziou; Qi Zhou; Diane Heels-Ansdell; Stephen D Walter; Gordon H Guyatt; David N Flynn; Mohamed B Elamin; Mohammad Hassan Murad; Nisrin O Abu Elnour; Julianna F Lampropulos; Amit Sood; Rebecca J Mullan; Patricia J Erwin; Clare R Bankhead; Rafael Perera; Carolina Ruiz Culebro; John J You; Sohail M Mulla; Jagdeep Kaur; Kara A Nerenberg; Holger Schünemann; Deborah J Cook; Kristina Lutz; Christine M Ribic; Noah Vale; German Malaga; Elie A Akl; Ignacio Ferreira-Gonzalez; Pablo Alonso-Coello; Gerard Urrutia; Regina Kunz; Heiner C Bucher; Alain J Nordmann; Heike Raatz; Suzana Alves da Silva; Fabio Tuche; Brigitte Strahm; Benjamin Djulbegovic; Neill K J Adhikari; Edward J Mills; Femida Gwadry-Sridhar; Haresh Kirpalani; Heloisa P Soares; Paul J Karanicolas; Karen E A Burns; Per Olav Vandvik; Fernando Coto-Yglesias; Pedro Paulo M Chrispim; Tim Ramsay
Journal:  JAMA       Date:  2010-03-24       Impact factor: 56.272

3.  Bias and trials stopped early for benefit.

Authors:  Scott M Berry; Bradley P Carlin; Jason Connor
Journal:  JAMA       Date:  2010-07-14       Impact factor: 56.272

4.  Current controversies in data monitoring for clinical trials.

Authors:  Stuart J Pocock
Journal:  Clin Trials       Date:  2006       Impact factor: 2.486

5.  Are Bayes' days upon us? Statistical methods could change the conduct of clinical trials.

Authors:  Mary Beckman
Journal:  J Natl Cancer Inst       Date:  2006-11-01       Impact factor: 13.506

6.  Stopping at nothing? Some dilemmas of data monitoring in clinical trials.

Authors:  Steven N Goodman
Journal:  Ann Intern Med       Date:  2007-06-19       Impact factor: 25.391

Review 7.  Early stopping of randomized clinical trials for overt efficacy is problematic.

Authors:  Dirk Bassler; Victor M Montori; Matthias Briel; Paul Glasziou; Gordon Guyatt
Journal:  J Clin Epidemiol       Date:  2008-03       Impact factor: 6.437

8.  Does pravastatin promote cancer in elderly patients? A meta-analysis.

Authors:  Stefanos Bonovas; Nikolaos M Sitaras
Journal:  CMAJ       Date:  2007-02-27       Impact factor: 8.262

Review 9.  Justification for the Use of Statins in Primary Prevention: an Intervention Trial Evaluating Rosuvastatin (JUPITER)--can C-reactive protein be used to target statin therapy in primary prevention?

Authors:  Samia Mora; Paul M Ridker
Journal:  Am J Cardiol       Date:  2005-12-01       Impact factor: 2.778

10.  Stopping randomized trials early for benefit: a protocol of the Study Of Trial Policy Of Interim Truncation-2 (STOPIT-2).

Authors:  Matthias Briel; Melanie Lane; Victor M Montori; Dirk Bassler; Paul Glasziou; German Malaga; Elie A Akl; Ignacio Ferreira-Gonzalez; Pablo Alonso-Coello; Gerard Urrutia; Regina Kunz; Carolina Ruiz Culebro; Suzana Alves da Silva; David N Flynn; Mohamed B Elamin; Brigitte Strahm; M Hassan Murad; Benjamin Djulbegovic; Neill K J Adhikari; Edward J Mills; Femida Gwadry-Sridhar; Haresh Kirpalani; Heloisa P Soares; Nisrin O Abu Elnour; John J You; Paul J Karanicolas; Heiner C Bucher; Julianna F Lampropulos; Alain J Nordmann; Karen E A Burns; Sohail M Mulla; Heike Raatz; Amit Sood; Jagdeep Kaur; Clare R Bankhead; Rebecca J Mullan; Kara A Nerenberg; Per Olav Vandvik; Fernando Coto-Yglesias; Holger Schünemann; Fabio Tuche; Pedro Paulo M Chrispim; Deborah J Cook; Kristina Lutz; Christine M Ribic; Noah Vale; Patricia J Erwin; Rafael Perera; Qi Zhou; Diane Heels-Ansdell; Tim Ramsay; Stephen D Walter; Gordon H Guyatt
Journal:  Trials       Date:  2009-07-06       Impact factor: 2.279

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  1 in total

1.  Optimal designs for phase II/III drug development programs including methods for discounting of phase II results.

Authors:  Stella Erdmann; Marietta Kirchner; Heiko Götte; Meinhard Kieser
Journal:  BMC Med Res Methodol       Date:  2020-10-09       Impact factor: 4.615

  1 in total

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