Evidence map›Paper›PMID 26812695›Full record

ArticleBiometrics2016

Global rank tests for multiple, possibly censored, outcomes.

Ritesh Ramchandani, David A Schoenfeld, Dianne M Finkelstein

Open access · greenAbstract read
In one paragraph

Article in Biometrics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.3field-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

20 citing papers in PubMed, 48 citations in OpenAlex.

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  13. Semiparametric regression modeling of the global percentile outcome.Journal of statistical planning and inference · 2023
    Article
  14. Article
  15. Article
  16. Applying a Risk-benefit Analysis to Outcomes in Tuberculosis Clinical Trials.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2020
    Article
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  18. Review
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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 at 1 institution in 1 country.

Ritesh RamchandaniDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, 677 Huntington Ave Boston, Massachusetts 02115, U.S.A.. ritesh@mail.harvard.edu.
David A SchoenfeldDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, 677 Huntington Ave Boston, Massachusetts 02115, U.S.A.
Dianne M FinkelsteinDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, 677 Huntington Ave Boston, Massachusetts 02115, U.S.A.
Harvard University · US

Funding

Training Grant in Quantitative Sciences for Cancer ResearchT32CA009337 · NCI · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI QUACKENBUSH, JOHN, TRIPPA, LORENZO · 1986 to 2025
$12.3M
Training in Neurostatistics and NeuroepidemiologyT32NS048005 · NINDS · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI ONNELA, JUKKA-PEKKA · 2004 to 2018
$3.2M
NINDS NIH HHS T32 NS048005
6 · The paper itself

Abstract

Clinical trials often collect multiple outcomes on each patient, as the treatment may be expected to affect the patient on many dimensions. For example, a treatment for a neurological disease such as ALS is intended to impact several dimensions of neurological function as well as survival. The assessment of treatment on the basis of multiple outcomes is challenging, both in terms of selecting a test and interpreting the results. Several global tests have been proposed, and we provide a general approach to selecting and executing a global test. The tests require minimal parametric assumptions, are flexible about weighting of the various outcomes, and are appropriate even when some or all of the outcomes are censored. The test we propose is based on a simple scoring mechanism applied to each pair of subjects for each endpoint. The pairwise scores are then reduced to a summary score, and a rank-sum test is applied to the summary scores. This can be seen as a generalization of previously proposed nonparametric global tests (e.g., O'Brien, 1984). We discuss the choice of optimal weighting schemes based on power and relative importance of the outcomes. As the optimal weights are generally unknown in practice, we also propose an adaptive weighting scheme and evaluate its performance in simulations. We apply the methods to analyze the impact of a treatment on neurological function and death in an ALS trial.

Indexed as

Data Interpretation, StatisticalStatistics, NonparametricTreatment OutcomeAmyotrophic Lateral SclerosisClinical Trials as TopicComputer SimulationHumansNervous SystemSurvival AnalysisALSGlobal testMultiple endpointsNonparametricRank-sumU-statistic

Identifiers

PMID26812695
PMCPMC4960007
OpenAlexW2255997205

What OpenQuestion holds

Textmetadata
LicenceTDM
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.