Evidence map›Paper›PMID 25551580›Full record

ArticleHealth and quality of life outcomes2014

Comparison of three longitudinal analysis models for the health-related quality of life in oncology: a simulation study.

Amélie Anota, Antoine Barbieri, Marion Savina, Alhousseiny Pam, Sophie Gourgou-Bourgade, Franck Bonnetain, Caroline Bascoul-Mollevi

Abstract read
In one paragraph

Article in Health and quality of life outcomes, 2014. 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
–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

10 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Longitudinal analysis of health-related quality of life in cancer clinical trials: methods and interpretation of results.Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation · 2021
    Article
  8. Article
  9. Review
  10. 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

7 authors.

Amélie AnotaQuality of Life in Oncology National Platform, Besançon, France. aanota@chu-besancon.fr.
Antoine BarbieriBiostatistic unit, Institut régional du Cancer de Montpellier (ICM) - Val d'Aurelle, Montpellier, France. Antoine.Barbieri@icm.unicancer.fr.
Marion SavinaINSERM, Clinical and EpidemiologicalResearch Unit (CIC-EC 7) - CTD INCa, Institut Bergonié, Bordeaux, France. Marion.Savina@isped.u-bordeaux2.fr.
Alhousseiny PamMethodological and Quality of Life in Oncology Unit, EA 3181, University Hospital of Besançon, Besançon, France. apam@chu-besancon.fr.
Sophie Gourgou-BourgadeBiostatistic unit, Institut régional du Cancer de Montpellier (ICM) - Val d'Aurelle, Montpellier, France. Sophie.Gourgou@icm.unicancer.fr.
Franck BonnetainQuality of Life in Oncology National Platform, Besançon, France. franck.bonnetain@univ-fcomte.fr.
Caroline Bascoul-MolleviBiostatistic unit, Institut régional du Cancer de Montpellier (ICM) - Val d'Aurelle, Montpellier, France. Caroline.Mollevi@icm.unicancer.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHealth-Related Quality of Life (HRQoL) is an important endpoint in oncology clinical trials aiming to investigate the clinical benefit of new therapeutic strategies for the patient. However, the longitudinal analysis of HRQoL remains complex and unstandardized. There is clearly a need to propose accessible statistical methods and meaningful results for clinicians. The objective of this study was to compare three strategies for longitudinal analyses of HRQoL data in oncology clinical trials through a simulation study.

methodsThe methods proposed were: the score and mixed model (SM); a survival analysis approach based on the time to HRQoL score deterioration (TTD); and the longitudinal partial credit model (LPCM). Simulations compared the methods in terms of type I error and statistical power of the test of an interaction effect between treatment arm and time. Several simulation scenarios were explored based on the EORTC HRQoL questionnaires and varying the number of patients (100, 200 or 300), items (1, 2 or 4) and response categories per item (4 or 7). Five or 10 measurement times were considered, with correlations ranging from low to high between each measure. The impact of informative missing data on these methods was also studied to reflect the reality of most clinical trials.

resultsWith complete data, the type I error rate was close to the expected value (5%) for all methods, while the SM method was the most powerful method, followed by LPCM. The power of TTD is low for single-item dimensions, because only four possible values exist for the score. When the number of items increases, the power of the SM approach remained stable, those of the TTD method increases while the power of LPCM remained stable. With 10 measurement times, the LPCM was less efficient. With informative missing data, the statistical power of SM and TTD tended to decrease, while that of LPCM tended to increase.

conclusionsTo conclude, the SM model was the most powerful model, irrespective of the scenario considered, and the presence or not of missing data. The TTD method should be avoided for single-item dimensions of the EORTC questionnaire. While the LPCM model was more adapted to this kind of data, it was less efficient than the SM model. These results warrant validation through comparisons on real data.

Indexed as

Health Status IndicatorsModels, TheoreticalPatient Outcome AssessmentFemaleHealth StatusHumansLongitudinal StudiesMaleMedical OncologyNeoplasmsQuality of Life

Identifiers

PMID25551580
PMCPMC4326524

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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.