Literature DB >> 12689733

Elicitation of prior distributions for a phase III randomized controlled trial of adjuvant therapy with surgery for hepatocellular carcinoma.

Say-Beng Tan1, Y-F Alexander Chung, Bee-Choo Tai, Yin-Bun Cheung, David Machin.   

Abstract

A randomized, controlled clinical trial of radioactive iodine tagged with lipiodol in patients with resected hepatocellular carcinoma was criticized for its early stopping and resulting small sample size. To clarify its results, a new, larger multicenter trial was therefore proposed. This paper describes the elicitation of the pretrial opinions of the investigators involved in the new trial and the construction of appropriate clinical and skeptical prior distributions based on their responses. The prior distributions provide a useful tool in assessing the state of equipoise before the start of the trial. They can also be used in Bayesian analyses, both at the interim stage(s) as well as at the end of the trial. We illustrate these analyses, assuming that the data resulting from the new trial was the same as that obtained in the earlier trial when it was stopped.

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Year:  2003        PMID: 12689733     DOI: 10.1016/s0197-2456(02)00318-5

Source DB:  PubMed          Journal:  Control Clin Trials        ISSN: 0197-2456


  11 in total

1.  Gerontologic biostatistics: the statistical challenges of clinical research with older study participants.

Authors:  Peter H Van Ness; Peter A Charpentier; Edward H Ip; Xiaoyan Leng; Terrence E Murphy; Janet A Tooze; Heather G Allore
Journal:  J Am Geriatr Soc       Date:  2010-06-01       Impact factor: 5.562

Review 2.  Strategy for randomised clinical trials in rare cancers.

Authors:  Say-Beng Tan; Keith B G Dear; Paolo Bruzzi; David Machin
Journal:  BMJ       Date:  2003-07-05

3.  Interpreting trial results in light of conflicting evidence: a Bayesian analysis of adjuvant chemotherapy for non-small-cell lung cancer.

Authors:  Rebecca A Miksad; Mithat Gönen; Thomas J Lynch; Thomas G Roberts
Journal:  J Clin Oncol       Date:  2009-03-23       Impact factor: 44.544

4.  A Bayesian approach for population pharmacokinetic modelling of sirolimus.

Authors:  Chantaratsamon Dansirikul; Raymond G Morris; Susan E Tett; Stephen B Duffull
Journal:  Br J Clin Pharmacol       Date:  2006-10       Impact factor: 4.335

5.  Elicitation of expert prior opinion: application to the MYPAN trial in childhood polyarteritis nodosa.

Authors:  Lisa V Hampson; John Whitehead; Despina Eleftheriou; Catrin Tudur-Smith; Rachel Jones; David Jayne; Helen Hickey; Michael W Beresford; Claudia Bracaglia; Afonso Caldas; Rolando Cimaz; Joke Dehoorne; Pavla Dolezalova; Mark Friswell; Marija Jelusic; Stephen D Marks; Neil Martin; Anne-Marie McMahon; Joachim Peitz; Annet van Royen-Kerkhof; Oguz Soylemezoglu; Paul A Brogan
Journal:  PLoS One       Date:  2015-03-30       Impact factor: 3.240

6.  Bayesian methods for the design and interpretation of clinical trials in very rare diseases.

Authors:  Lisa V Hampson; John Whitehead; Despina Eleftheriou; Paul Brogan
Journal:  Stat Med       Date:  2014-06-23       Impact factor: 2.373

Review 7.  Clinical trial designs for rare diseases: studies developed and discussed by the International Rare Cancers Initiative.

Authors:  Jan Bogaerts; Matthew R Sydes; Nicola Keat; Andrea McConnell; Al Benson; Alan Ho; Arnaud Roth; Catherine Fortpied; Cathy Eng; Clare Peckitt; Corneel Coens; Curtis Pettaway; Dirk Arnold; Emma Hall; Ernie Marshall; Francesco Sclafani; Helen Hatcher; Helena Earl; Isabelle Ray-Coquard; James Paul; Jean-Yves Blay; Jeremy Whelan; Kathy Panageas; Keith Wheatley; Kevin Harrington; Lisa Licitra; Lucinda Billingham; Martee Hensley; Martin McCabe; Poulam M Patel; Richard Carvajal; Richard Wilson; Rob Glynne-Jones; Rob McWilliams; Serge Leyvraz; Sheela Rao; Steve Nicholson; Virginia Filiaci; Anastassia Negrouk; Denis Lacombe; Elisabeth Dupont; Iris Pauporté; John J Welch; Kate Law; Ted Trimble; Matthew Seymour
Journal:  Eur J Cancer       Date:  2014-12-24       Impact factor: 9.162

8.  Design and conduct of a provider survey to determine a clinically persuasive effect size in planning VA Cooperative Study #590 (Li+).

Authors:  Kelly M Harrington; Matthew H Liang; Keri Hannagan; Soe Soe Thwin; Ryan E Ferguson; Natalie Morgenstern; Erick Flores; Ira R Katz
Journal:  Contemp Clin Trials Commun       Date:  2016-08-31

9.  Bayesian treatment comparison using parametric mixture priors computed from elicited histograms.

Authors:  Peter F Thall; Moreno Ursino; Véronique Baudouin; Corinne Alberti; Sarah Zohar
Journal:  Stat Methods Med Res       Date:  2017-09-05       Impact factor: 3.021

10.  Assurance calculations for planning clinical trials with time-to-event outcomes.

Authors:  Shijie Ren; Jeremy E Oakley
Journal:  Stat Med       Date:  2013-07-16       Impact factor: 2.373

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