Evidence map›Paper›PMID 36966273›Full record

ArticleBMC medical research methodology2023

A new cure model that corrects for increased risk of non-cancer death: analysis of reliability and robustness, and application to real-life data.

Laura Botta, Juste Goungounga, Riccardo Capocaccia, Gaelle Romain, Marc Colonna, Gemma Gatta, Olayidé Boussari, Valérie Jooste

Open access · goldFull text read
In one paragraph

Article in BMC medical research methodology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Fitting high-dimensional mixture cure models using the hdcuremodelsR package.Computer methods and programs in biomedicine · 2026
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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

8 authors at 6 institutions in 2 countries.

Laura Botta *Evaluative Epidemiology Unit, Department of Epidemiology and Data Science, Fondazione IRCCS "Istituto nazionale dei Tumori", Via Venezian 1, 20133, Milan, Italy. laura.botta@istitutotumori.mi.it.
Juste Goungounga *Registre Bourguignon des Cancers Digestifs, Dijon-Bourgogne University Hospital, F-21000, Dijon, France.
Riccardo CapocacciaEditorial Board, Epidemiologia e Prevenzione, Milan, Italy.
Gaelle RomainRegistre Bourguignon des Cancers Digestifs, Dijon-Bourgogne University Hospital, F-21000, Dijon, France.
Marc ColonnaIsere Cancer Registry, Centre Hospitalier Universitaire Grenoble-Alpes, 38043, Grenoble Cedex 9, France.
Gemma GattaEvaluative Epidemiology Unit, Department of Epidemiology and Data Science, Fondazione IRCCS "Istituto nazionale dei Tumori", Via Venezian 1, 20133, Milan, Italy.
Olayidé BoussariUMR 1231, EPICAD team, INSERM, Université Bourgogne-Franche-Comté, Dijon, France.
Valérie JoosteRegistre Bourguignon des Cancers Digestifs, Dijon-Bourgogne University Hospital, F-21000, Dijon, France.
Fondazione IRCCS Istituto Nazionale dei Tumori · ITInserm · FRCentre Hospitalier Universitaire de Grenoble · FRFondazione Progetto Ematologia · ITLaboratoire de Physique des 2 Infinis Irène Joliot-Curie · FRUniversité Bourgogne Franche-Comté · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNon-cancer mortality in cancer patients may be higher than overall mortality in the general population due to a combination of factors, such as long-term adverse effects of treatments, and genetic, environmental or lifestyle-related factors. If so, conventional indicators may underestimate net survival and cure fraction. Our aim was to propose and evaluate a mixture cure survival model that takes into account the increased risk of non-cancer death for cancer patients.

methodsWe assessed the performance of a corrected mixture cure survival model derived from a conventional mixture cure model to estimate the cure fraction, the survival of uncured patients, and the increased risk of non-cancer death in two settings of net survival estimation, grouped life-table data and individual patients' data. We measured the model's performance in terms of bias, standard deviation of the estimates and coverage rate, using an extensive simulation study. This study included reliability assessments through violation of some of the model's assumptions. We also applied the models to colon cancer data from the FRANCIM network.

resultsWhen the assumptions were satisfied, the corrected cure model provided unbiased estimates of parameters expressing the increased risk of non-cancer death, the cure fraction, and net survival in uncured patients. No major difference was found when the model was applied to individual or grouped data. The absolute bias was < 1% for all parameters, while coverage ranged from 89 to 97%. When some of the assumptions were violated, parameter estimates appeared more robust when obtained from grouped than from individual data. As expected, the uncorrected cure model performed poorly and underestimated net survival and cure fractions in the simulation study. When applied to colon cancer real-life data, cure fractions estimated using the proposed model were higher than those in the conventional model, e.g. 5% higher in males at age 60 (57% vs. 52%).

conclusionsThe present analysis supports the use of the corrected mixture cure model, with the inclusion of increased risk of non-cancer death for cancer patients to provide better estimates of indicators based on cancer survival. These are important to public health decision-making; they improve patients' awareness and facilitate their return to normal life.

Indexed as

Colonic NeoplasmsComputer SimulationHumansMaleMiddle AgedModels, StatisticalReproducibility of ResultsSurvival AnalysisSurvival RateCancerCure modelIncreased non-cancer mortalityLife tablesNet survivalPopulation-based dataReliabilityRobustness

Identifiers

PMID36966273
PMCPMC10040108
OpenAlexW4360946566

What OpenQuestion holds

Textfull text, public
LicenceCC BY
reference markers read1
measurements read734
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.