Evidence map›Paper›PMID 31096911›Full record

ArticleBMC medical research methodology2019

Correcting for misclassification and selection effects in estimating net survival in clinical trials.

Juste Aristide Goungounga, Célia Touraine, Nathalie Grafféo, Roch Giorgi, CENSUR working survival group

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Article in BMC medical research methodology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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0cells of the map it votes in
3citing papers in PubMed
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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

3 citing papers in PubMed.

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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

5 authors.

Juste Aristide GoungoungaAix Marseille Univ, INSERM, IRD, SESSTIM Sciences Economiques & Sociales de la Santé & Traitement de l'Information Médicale, Marseille, France.
Célia TouraineAix Marseille Univ, INSERM, IRD, SESSTIM Sciences Economiques & Sociales de la Santé & Traitement de l'Information Médicale, Marseille, France.
Nathalie GrafféoINSERM U1153, Centre of Research in Epidemiology and Statistics Sorbonne Paris Cité (CRESS), ECSTRA Team, Hôpital Saint Louis, Paris, France.
Roch GiorgiAix Marseille Univ, APHM, INSERM, IRD, SESSTIM (Sciences Economiques & Sociales de la Santé & Traitement de l'Information Médicale), Hop Timone, BioSTIC (Biostatistique et Technologies de l'Information et de la Communication), Marseille, France. roch.giorgi@univ-amu.fr.ORCID 0000-0001-6135-3078
CENSUR working survival group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNet survival, a measure of the survival where the patients would only die from the cancer under study, may be compared between treatment groups using either "cause-specific methods", when the causes of death are known and accurate, or "population-based methods", when the causes are missing or inaccurate. The latter methods rely on the assumption that mortality due to other causes than cancer is the same as the expected mortality in the general population with same demographic characteristics derived from population life tables. This assumption may not hold in clinical trials where patients are likely to be quite different from the general population due to some criteria for patient selection.

methodsIn this work, we propose and assess the performance of a new flexible population-based model to estimate long-term net survival in clinical trials and that allows for cause-of-death misclassification and for effects of selection. Comparisons were made with cause-specific and other population-based methods in a simulation study and in an application to prostate cancer clinical trial data.

resultsIn estimating net survival, cause-specific methods seemed to introduce important biases associated with the degree of misclassification of cancer deaths. The usual population-based method provides also biased estimates, depending on the strength of the selection effect. Compared to these methods, the new model was able to provide more accurate estimates of net survival in long-term clinical trials.

conclusionFinally, the new model paves the way for new methodological developments in the field of net survival methods in multicenter clinical trials.

Indexed as

Data AccuracySurvival AnalysisAgedCause of DeathClinical Trials as TopicComputer SimulationDiethylstilbestrolHumansMaleProstatic NeoplasmsResearch DesignDiethylstilbestrolCancer clinical trialsCause of deathExcess hazard modelLife tablesNet survivalSelection bias

Identifiers

PMID31096911
PMCPMC6524224

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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.