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

BACKGROUND: Health-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...

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Autores principales: Anota, Amélie, Barbieri, Antoine, Savina, Marion, Pam, Alhousseiny, Gourgou-Bourgade, Sophie, Bonnetain, Franck, Bascoul-Mollevi, Caroline
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4326524/
https://www.ncbi.nlm.nih.gov/pubmed/25551580
http://dx.doi.org/10.1186/s12955-014-0192-2
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author Anota, Amélie
Barbieri, Antoine
Savina, Marion
Pam, Alhousseiny
Gourgou-Bourgade, Sophie
Bonnetain, Franck
Bascoul-Mollevi, Caroline
author_facet Anota, Amélie
Barbieri, Antoine
Savina, Marion
Pam, Alhousseiny
Gourgou-Bourgade, Sophie
Bonnetain, Franck
Bascoul-Mollevi, Caroline
author_sort Anota, Amélie
collection PubMed
description BACKGROUND: Health-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. METHODS: The 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. RESULTS: With 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. CONCLUSIONS: To 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. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12955-014-0192-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-43265242015-02-14 Comparison of three longitudinal analysis models for the health-related quality of life in oncology: a simulation study Anota, Amélie Barbieri, Antoine Savina, Marion Pam, Alhousseiny Gourgou-Bourgade, Sophie Bonnetain, Franck Bascoul-Mollevi, Caroline Health Qual Life Outcomes Research BACKGROUND: Health-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. METHODS: The 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. RESULTS: With 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. CONCLUSIONS: To 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. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12955-014-0192-2) contains supplementary material, which is available to authorized users. BioMed Central 2014-12-31 /pmc/articles/PMC4326524/ /pubmed/25551580 http://dx.doi.org/10.1186/s12955-014-0192-2 Text en © Anota et al.; licensee BioMed Central. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Anota, Amélie
Barbieri, Antoine
Savina, Marion
Pam, Alhousseiny
Gourgou-Bourgade, Sophie
Bonnetain, Franck
Bascoul-Mollevi, Caroline
Comparison of three longitudinal analysis models for the health-related quality of life in oncology: a simulation study
title Comparison of three longitudinal analysis models for the health-related quality of life in oncology: a simulation study
title_full Comparison of three longitudinal analysis models for the health-related quality of life in oncology: a simulation study
title_fullStr Comparison of three longitudinal analysis models for the health-related quality of life in oncology: a simulation study
title_full_unstemmed Comparison of three longitudinal analysis models for the health-related quality of life in oncology: a simulation study
title_short Comparison of three longitudinal analysis models for the health-related quality of life in oncology: a simulation study
title_sort comparison of three longitudinal analysis models for the health-related quality of life in oncology: a simulation study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4326524/
https://www.ncbi.nlm.nih.gov/pubmed/25551580
http://dx.doi.org/10.1186/s12955-014-0192-2
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