Evidence map›Paper›PMID 28612371›Full record

ArticleStatistics in medicine2017

Estimation in multi-arm two-stage trials with treatment selection and time-to-event endpoint.

Matthias Brückner, Andrew Titman, Thomas Jaki

Abstract read
In one paragraph

Article in Statistics in medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 1 synthesis or guideline pooled it.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Matthias BrücknerDepartment of Mathematics and Statistics, Lancaster University, Lancaster, LA1 4YF, U.K.ORCID http://orcid.org/0000-0002-6103-9895
Andrew TitmanDepartment of Mathematics and Statistics, Lancaster University, Lancaster, LA1 4YF, U.K.ORCID http://orcid.org/0000-0003-2084-0720
Thomas JakiDepartment of Mathematics and Statistics, Lancaster University, Lancaster, LA1 4YF, U.K.

Funding

Department of Health SRF-2015-08-001Medical Research Council MR/M005755/1
6 · The paper itself

Abstract

We consider estimation of treatment effects in two-stage adaptive multi-arm trials with a common control. The best treatment is selected at interim, and the primary endpoint is modeled via a Cox proportional hazards model. The maximum partial-likelihood estimator of the log hazard ratio of the selected treatment will overestimate the true treatment effect in this case. Several methods for reducing the selection bias have been proposed for normal endpoints, including an iterative method based on the estimated conditional selection biases and a shrinkage approach based on empirical Bayes theory. We adapt these methods to time-to-event data and compare the bias and mean squared error of all methods in an extensive simulation study and apply the proposed methods to reconstructed data from the FOCUS trial. We find that all methods tend to overcorrect the bias, and only the shrinkage methods can reduce the mean squared error. © 2017 The Authors. Statistics in Medicine Published by John Wiley & Sons Ltd.

Indexed as

Adaptive Clinical Trials as TopicBayes TheoremBiostatisticsClinical Trials as TopicColorectal NeoplasmsComputer SimulationConfidence IntervalsControlled Clinical Trials as TopicHumansKaplan-Meier EstimateLikelihood FunctionsSelection BiasTime Factorsadaptive designbiasempirical Bayesmulti-arm trialtime-to-event

Identifiers

PMID28612371
PMCPMC5575545

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.