Evidence map›Paper›PMID 28853158›Full record

ArticleBiometrics2018

A pairwise likelihood augmented Cox estimator for left-truncated data.

Fan Wu, Sehee Kim, Jing Qin, Rajiv Saran, Yi Li

Abstract read
In one paragraph

Article in Biometrics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–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

2 citing papers in PubMed.

  1. Article
  2. Article
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

5 authors.

Fan WuDepartment of Biostatistics, University of Michigan, Ann Arbor, Michigan 48109, U.S.A.ORCID 0000-0002-1354-0546
Sehee KimDepartment of Biostatistics, University of Michigan, Ann Arbor, Michigan 48109, U.S.A.ORCID 0000-0002-1815-6957
Jing QinBiostatistics Research Branch, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892, U.S.A.
Rajiv SaranKidney Epidemiology and Cost Center, University of Michigan, Ann Arbor, Michigan 48109, U.S.A.
Yi LiDepartment of Biostatistics, University of Michigan, Ann Arbor, Michigan 48109, U.S.A.

Funding

The Boston Lung Cancer Survival CohortU01CA209414 · NCI · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI David C Christiani · 2017 to 2026
$12.2M
Cutting Edge Survival Methods for Epidemiological DataR01AG056764 · NIA · UNIVERSITY OF CALIFORNIA-IRVINE · PI NAN, BIN · 2018 to 2021
$1.3M
Functional Regression and Subgroup Analysis for Asynchronous Longitudinal Data.R21AG058198 · NIA · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI LI, YEHUA, LI, YI · 2018 to 2019
$422k
NCI NIH HHS U01 CA209414NIA NIH HHS R01 AG056764NIA NIH HHS R21 AG058198
6 · The paper itself

Abstract

Survival data collected from a prevalent cohort are subject to left truncation and the analysis is challenging. Conditional approaches for left-truncated data could be inefficient as they ignore the information in the marginal likelihood of the truncation times. Length-biased sampling methods may improve the estimation efficiency but only when the underlying truncation time is uniform; otherwise, they may generate biased estimates. We propose a semiparametric method for left-truncated data under the Cox model with no parametric distributional assumption about the truncation times. Our approach is to make inference based on the conditional likelihood augmented with a pairwise likelihood, which eliminates the truncation distribution, yet retains the information about the regression coefficients and the baseline hazard function in the marginal likelihood. An iterative algorithm is provided to solve for the regression coefficients and the baseline hazard function simultaneously. By empirical process and U-process theories, it has been shown that the proposed estimator is consistent and asymptotically normal with a closed-form consistent variance estimator. Simulation studies show substantial efficiency gain of our estimator in both the regression coefficients and the cumulative baseline hazard function over the conditional approach estimator. When the uniform truncation assumption holds, our estimator enjoys smaller biases and efficiency comparable to that of the full maximum likelihood estimator. An application to the analysis of a chronic kidney disease cohort study illustrates the utility of the method.

Indexed as

Data Interpretation, StatisticalProportional Hazards ModelsSurvival AnalysisAlgorithmsBiasComputer SimulationHumansLikelihood FunctionsModels, StatisticalRenal Insufficiency, ChronicChronic kidney diseaseComposite likelihoodEmpirical processSelf-consistencyU-process

Identifiers

PMID28853158
PMCPMC6402872

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Registered trials

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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.