Evidence map›Paper›PMID 29035083›Full record

ArticleClinical trials (London, England)2018

Multiplicity-adjusted semiparametric benefiting subgroup identification in clinical trials.

Patrick M Schnell, Peter Müller, Qi Tang, Bradley P Carlin

Open access · greenAbstract read
In one paragraph

Article in Clinical trials (London, England), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.7field-weighted citation impact, top 12% of its field
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

4 citing papers in PubMed, 15 citations in OpenAlex.

  1. [Subgroup identification based on accelerated failure time model combined with adaptive elastic net].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2021
    Article
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  4. Review
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

4 authors at 4 institutions in 1 country.

Patrick M Schnell1 Division of Biostatistics, College of Public Health, The Ohio State University, Columbus, OH, USA.
Peter Müller2 Department of Mathematics, The University of Texas at Austin, Austin, TX, USA.
Qi Tang3 Former employee of AbbVie, AbbVie, North Chicago, IL, USA.
Bradley P Carlin5 Division of Biostatistics, School of Public Health, University of Minnesota, Minneapolis, MN, USA.
Sanofi (United States) · USThe Ohio State University · USThe University of Texas at Austin · USUniversity of Minnesota · US

Funding

Statistical Methods and Software for More Efficient, Ethical, and Affordable ClinR01CA157458 · NCI · UNIVERSITY OF MINNESOTA · PI CARLIN, BRADLEY P · 2012 to 2014
$939k
NCI NIH HHS R01 CA157458
6 · The paper itself

Abstract

Background A recent focus in the health sciences has been the development of personalized medicine, which includes determining the population for which a given treatment is effective. Due to limited data, identifying the true benefiting population is a challenging task. To tackle this difficulty, the credible subgroups approach provides a pair of bounding subgroups for the true benefiting subgroup, constructed so that one is contained by the benefiting subgroup while the other contains the benefiting subgroup with high probability. However, the method has so far only been developed for parametric linear models. Methods In this article, we develop the details required to follow the credible subgroups approach in more realistic settings by considering nonlinear and semiparametric regression models, supported for regulatory science by conditional power simulations. We also present an improved multiple testing approach using a step-down procedure. We evaluate our approach via simulations and apply it to data from four trials of Alzheimer's disease treatments carried out by AbbVie. Results Semiparametric modeling yields credible subgroups that are more robust to violations of linear treatment effect assumptions, and careful choice of the population of interest as well as the step-down multiple testing procedure result in a higher rate of detection of benefiting types of patients. The approach allows us to identify types of patients that benefit from treatment in the Alzheimer's disease trials. Conclusion Attempts to identify benefiting subgroups of patients in clinical trials are often met with skepticism due to a lack of multiplicity control and unrealistically restrictive assumptions. Our proposed approach merges two techniques, credible subgroups, and semiparametric regression, which avoids these problems and makes benefiting subgroup identification practical and reliable.

Indexed as

Models, StatisticalAge FactorsAlgorithmsAlzheimer DiseaseClinical Trials as TopicComputer SimulationHumansMonte Carlo MethodPrecision MedicineRegression AnalysisResearch DesignSeverity of Illness IndexSex FactorsBayesian inferenceclinical trialsmultiple testingpersonalized medicinesemiparametric regressionsubgroup identification

Identifiers

PMID29035083
PMCPMC8796253
OpenAlexW2766099423

What OpenQuestion holds

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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.