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Published in: BMC Medical Research Methodology 1/2020

Open Access 01-12-2020 | Esophageal Cancer | Research article

Handling informative dropout in longitudinal analysis of health-related quality of life: application of three approaches to data from the esophageal cancer clinical trial PRODIGE 5/ACCORD 17

Authors: B. Cuer, C. Mollevi, A. Anota, E. Charton, B. Juzyna, T. Conroy, C. Touraine

Published in: BMC Medical Research Methodology | Issue 1/2020

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Abstract

Background

Health-related quality of life (HRQoL) has become a major endpoint to assess the clinical benefit of new therapeutic strategies in oncology clinical trials. Typically, HRQoL outcomes are analyzed using linear mixed models (LMMs). However, longitudinal analysis of HRQoL in the presence of missing data remains complex and unstandardized. Our objective was to compare the modeling alternatives that account for informative dropout.

Methods

We investigated three alternative methods—the selection model (SM), pattern-mixture model (PMM), and shared-parameters model (SPM)—in relation to the LMM. We first compared them on the basis of methodological arguments highlighting their advantages and drawbacks. Then, we applied them to data from a randomized clinical trial that included 267 patients with advanced esophageal cancer for the analysis of four HRQoL dimensions evaluated using the European Organisation for Research and Treatment of Cancer (EORTC) QLQ-C30 questionnaire.

Results

We highlighted differences in terms of outputs, interpretation, and underlying modeling assumptions; this methodological comparison could guide the choice of method according to the context. In the application, none of the four models detected a significant difference between the two treatment arms. The estimated effect of time on HRQoL varied according to the method: for all analyzed dimensions, the PMM estimated an effect that contrasted with those estimated by the SM and SPM; the LMM estimated effects were confirmed by the SM (on two of four HRQoL dimensions) and SPM (on three of four HRQoL dimensions).

Conclusions

The PMM, SM, or SPM should be used to confirm or invalidate the results of LMM analysis when informative dropout is suspected. Of these three alternative methods, the SPM appears to be the most interesting from both theoretical and practical viewpoints.

Trial registration

This study is registered with ClinicalTrials.​gov, number NCT00861094.
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Literature
1.
go back to reference Osoba D. Health-related quality of life and cancer clinical trials. Ther Adv Med Oncol. 2011;3:57–71.CrossRef Osoba D. Health-related quality of life and cancer clinical trials. Ther Adv Med Oncol. 2011;3:57–71.CrossRef
2.
3.
go back to reference Little RJA, Rubin DB. Statistical analysis with missing data. New York: Wiley; 1986. Little RJA, Rubin DB. Statistical analysis with missing data. New York: Wiley; 1986.
4.
go back to reference Fielding S, Ogbuagu A, Sivasubramaniam S, MacLennan G, Ramsay CR. Reporting and dealing with missing quality of life data in RCTs: has the picture changed in the last decade? Qual Life Res. 2016;25:2977–83.CrossRef Fielding S, Ogbuagu A, Sivasubramaniam S, MacLennan G, Ramsay CR. Reporting and dealing with missing quality of life data in RCTs: has the picture changed in the last decade? Qual Life Res. 2016;25:2977–83.CrossRef
5.
go back to reference Fairclough DL. Design and analysis of quality of life studies in clinical trials. Chapman and Hall/CRC. 2010.CrossRef Fairclough DL. Design and analysis of quality of life studies in clinical trials. Chapman and Hall/CRC. 2010.CrossRef
6.
go back to reference Cnaan A, Laird NM, Slasor P. Using the general linear mixed model to analyse unbalanced repeated measures and longitudinal data. Stat Med. 1997;16:2349–80.CrossRef Cnaan A, Laird NM, Slasor P. Using the general linear mixed model to analyse unbalanced repeated measures and longitudinal data. Stat Med. 1997;16:2349–80.CrossRef
7.
go back to reference Fielding S, Fayers PM, Loge JH, Jordhøy MS, Kaasa S. Methods for handling missing data in palliative care research. Palliat Med. 2006;20:791–8.CrossRef Fielding S, Fayers PM, Loge JH, Jordhøy MS, Kaasa S. Methods for handling missing data in palliative care research. Palliat Med. 2006;20:791–8.CrossRef
8.
go back to reference Hussain JA, White IR, Langan D, Johnson MJ, Currow DC, Torgerson DJ, et al. Missing data in randomized controlled trials testing palliative interventions pose a significant risk of bias and loss of power: a systematic review and meta-analyses. J Clin Epidemiol. 2016;74:57–65.CrossRef Hussain JA, White IR, Langan D, Johnson MJ, Currow DC, Torgerson DJ, et al. Missing data in randomized controlled trials testing palliative interventions pose a significant risk of bias and loss of power: a systematic review and meta-analyses. J Clin Epidemiol. 2016;74:57–65.CrossRef
9.
go back to reference Fairclough DL, Peterson HF, Chang V. Why are missing quality of life data a problem in clinical trials of cancer therapy? Stat Med. 1998;17:667–77.CrossRef Fairclough DL, Peterson HF, Chang V. Why are missing quality of life data a problem in clinical trials of cancer therapy? Stat Med. 1998;17:667–77.CrossRef
10.
go back to reference DeSouza CM, Legedza ATR, Sankoh AJ. An overview of practical approaches for handling missing data in clinical trials. J Biopharm Stat. 2009;19:1055–73.CrossRef DeSouza CM, Legedza ATR, Sankoh AJ. An overview of practical approaches for handling missing data in clinical trials. J Biopharm Stat. 2009;19:1055–73.CrossRef
11.
go back to reference Ibrahim JG, Molenberghs G. Missing data methods in longitudinal studies: a review. Test Madr Spain. 2009;18:1–43. Ibrahim JG, Molenberghs G. Missing data methods in longitudinal studies: a review. Test Madr Spain. 2009;18:1–43.
12.
go back to reference Hogan JW, Laird NM. Model-based approaches to analysing incomplete longitudinal and failure time data. Stat Med. 1997;16:259–72.CrossRef Hogan JW, Laird NM. Model-based approaches to analysing incomplete longitudinal and failure time data. Stat Med. 1997;16:259–72.CrossRef
13.
go back to reference Little RJA. Modeling the drop-out mechanism in repeated-measures studies. J Am Stat Assoc. 1995;90:1112–21.CrossRef Little RJA. Modeling the drop-out mechanism in repeated-measures studies. J Am Stat Assoc. 1995;90:1112–21.CrossRef
14.
go back to reference Tsiatis AA, Davidian M. Joint modeling of longitudinal and time-to-event data: an overview. Stat Sin. 2004:809–34. Tsiatis AA, Davidian M. Joint modeling of longitudinal and time-to-event data: an overview. Stat Sin. 2004:809–34.
15.
go back to reference Vonesh EF, Greene T, Schluchter MD. Shared parameter models for the joint analysis of longitudinal data and event times. Stat Med. 2006;25:143–63.CrossRef Vonesh EF, Greene T, Schluchter MD. Shared parameter models for the joint analysis of longitudinal data and event times. Stat Med. 2006;25:143–63.CrossRef
16.
17.
go back to reference Michiels B, Molenberghs G, Bijnens L, Vangeneugden T, Thijs H. Selection models and pattern-mixture models to analyse longitudinal quality of life data subject to drop-out. Stat Med. 2002;21:1023–41.CrossRef Michiels B, Molenberghs G, Bijnens L, Vangeneugden T, Thijs H. Selection models and pattern-mixture models to analyse longitudinal quality of life data subject to drop-out. Stat Med. 2002;21:1023–41.CrossRef
18.
go back to reference Bell ML, Fairclough DL. Practical and statistical issues in missing data for longitudinal patient-reported outcomes. Stat Methods Med Res. 2013;23:440–59.CrossRef Bell ML, Fairclough DL. Practical and statistical issues in missing data for longitudinal patient-reported outcomes. Stat Methods Med Res. 2013;23:440–59.CrossRef
19.
go back to reference Du H, Hahn EA, Cella D. The impact of missing data on estimation of health-related quality of life outcomes. Anal Randomized Longitud Clin Trial. 2011;11:134–44. Du H, Hahn EA, Cella D. The impact of missing data on estimation of health-related quality of life outcomes. Anal Randomized Longitud Clin Trial. 2011;11:134–44.
20.
go back to reference Conroy T, Galais M-P, Raoul J-L, Bouché O, Gourgou-Bourgade S, Douillard J-Y, et al. Definitive chemoradiotherapy with FOLFOX versus fluorouracil and cisplatin in patients with oesophageal cancer (PRODIGE5/ACCORD17): final results of a randomised, phase 2/3 trial. Lancet Oncol. 2014;15:305–14.CrossRef Conroy T, Galais M-P, Raoul J-L, Bouché O, Gourgou-Bourgade S, Douillard J-Y, et al. Definitive chemoradiotherapy with FOLFOX versus fluorouracil and cisplatin in patients with oesophageal cancer (PRODIGE5/ACCORD17): final results of a randomised, phase 2/3 trial. Lancet Oncol. 2014;15:305–14.CrossRef
21.
go back to reference Bascoul-Mollevi C, Gourgou S, Galais M-P, Raoul J-L, Bouché O, Douillard J-Y, et al. Health-related quality of life results from the PRODIGE 5/ACCORD 17 randomised trial of FOLFOX versus fluorouracil–cisplatin regimen in oesophageal cancer. Eur J Cancer. 2017;84:239–49.CrossRef Bascoul-Mollevi C, Gourgou S, Galais M-P, Raoul J-L, Bouché O, Douillard J-Y, et al. Health-related quality of life results from the PRODIGE 5/ACCORD 17 randomised trial of FOLFOX versus fluorouracil–cisplatin regimen in oesophageal cancer. Eur J Cancer. 2017;84:239–49.CrossRef
22.
go back to reference Aaronson NK, Ahmedzai S, Bergman B, Bullinger M, Cull A, Duez NJ, et al. The European Organization for Research and Treatment of Cancer QLQ-C30: a quality-of-life instrument for use in international clinical trials in oncology. JNCI J Natl Cancer Inst. 1993;85:365–76.CrossRef Aaronson NK, Ahmedzai S, Bergman B, Bullinger M, Cull A, Duez NJ, et al. The European Organization for Research and Treatment of Cancer QLQ-C30: a quality-of-life instrument for use in international clinical trials in oncology. JNCI J Natl Cancer Inst. 1993;85:365–76.CrossRef
23.
go back to reference Fayers P, Aaronson NK, Bjordal K, Groenvold M, Curran D, Bottomley A. EORTC QLQ-C30 scoring manual, European Organisation for Research and Treatment of Cancer. 3rd ed; 2001. Fayers P, Aaronson NK, Bjordal K, Groenvold M, Curran D, Bottomley A. EORTC QLQ-C30 scoring manual, European Organisation for Research and Treatment of Cancer. 3rd ed; 2001.
24.
go back to reference Diggle P, Kenward MG. Informative drop-out in longitudinal data analysis. J R Stat Soc: Ser C: Appl Stat. 1994;43:49–93. Diggle P, Kenward MG. Informative drop-out in longitudinal data analysis. J R Stat Soc: Ser C: Appl Stat. 1994;43:49–93.
25.
go back to reference Pauler DK, McCoy S, Moinpour C. Pattern mixture models for longitudinal quality of life studies in advanced stage disease. Stat Med. 2003;22:795–809.CrossRef Pauler DK, McCoy S, Moinpour C. Pattern mixture models for longitudinal quality of life studies in advanced stage disease. Stat Med. 2003;22:795–809.CrossRef
26.
go back to reference Pinheiro JC, Bates DM. Mixed-effects models in S and S-PLUS. N. Y: Springer; 2000.CrossRef Pinheiro JC, Bates DM. Mixed-effects models in S and S-PLUS. N. Y: Springer; 2000.CrossRef
27.
go back to reference Rizopoulos D. JM: an r package for the joint modelling of longitudinal and time-to-event data. J Stat Softw Artic. 2010;35:1–33. Rizopoulos D. JM: an r package for the joint modelling of longitudinal and time-to-event data. J Stat Softw Artic. 2010;35:1–33.
28.
go back to reference Thijs H, Molenberghs G, Michiels B, Verbeke G, Curran D. Strategies to fit pattern-mixture models. Biostatistics. 2002;3:245–65.CrossRef Thijs H, Molenberghs G, Michiels B, Verbeke G, Curran D. Strategies to fit pattern-mixture models. Biostatistics. 2002;3:245–65.CrossRef
29.
go back to reference Little RJA. Pattern-mixture models for multivariate incomplete data. J Am Stat Assoc. 1993;88:125–34. Little RJA. Pattern-mixture models for multivariate incomplete data. J Am Stat Assoc. 1993;88:125–34.
30.
go back to reference Verbeke G, Molenberghs G, Thijs H, Lesaffre E, Kenward MG. Sensitivity analysis for nonrandom dropout: a local influence approach. Biometrics. 2001;57:7–14.CrossRef Verbeke G, Molenberghs G, Thijs H, Lesaffre E, Kenward MG. Sensitivity analysis for nonrandom dropout: a local influence approach. Biometrics. 2001;57:7–14.CrossRef
31.
go back to reference Rizopoulos D, Verbeke G, Molenberghs G. Shared parameter models under random effects misspecification. Biometrika. 2008;95:63–74.CrossRef Rizopoulos D, Verbeke G, Molenberghs G. Shared parameter models under random effects misspecification. Biometrika. 2008;95:63–74.CrossRef
32.
go back to reference Rizopoulos D. The r package JMbayes for fitting joint models for longitudinal and time-to-event data using MCMC. J Stat Softw Artic. 2016;72:1–46. Rizopoulos D. The r package JMbayes for fitting joint models for longitudinal and time-to-event data using MCMC. J Stat Softw Artic. 2016;72:1–46.
33.
go back to reference Crowther MJ, Abrams KR, Lambert PC. Joint modeling of longitudinal and survival data. Stata J. 2013;13:165–84.CrossRef Crowther MJ, Abrams KR, Lambert PC. Joint modeling of longitudinal and survival data. Stata J. 2013;13:165–84.CrossRef
34.
go back to reference Garcia-Hernandez A, Rizopoulos D. %JM: A SAS macro to fit jointly generalized mixed models for longitudinal data and time-to-event responses. J Stat Softw Artic. 2018;84:1–29. Garcia-Hernandez A, Rizopoulos D. %JM: A SAS macro to fit jointly generalized mixed models for longitudinal data and time-to-event responses. J Stat Softw Artic. 2018;84:1–29.
35.
go back to reference Molenberghs G, Kenward M. Missing data in clinical studies: Wiley; 2007. Molenberghs G, Kenward M. Missing data in clinical studies: Wiley; 2007.
36.
go back to reference Calvert M, Blazeby J, Altman DG, Revicki DA, Moher D, Brundage MD, et al. Reporting of patient-reported outcomes in randomized trials: the CONSORT PRO extension. JAMA. 2013;309:814–22.CrossRef Calvert M, Blazeby J, Altman DG, Revicki DA, Moher D, Brundage MD, et al. Reporting of patient-reported outcomes in randomized trials: the CONSORT PRO extension. JAMA. 2013;309:814–22.CrossRef
37.
go back to reference Little RJ, D’agostino R, Cohen ML, Dickersin K, Emerson SS, Farrar JT, et al. The prevention and treatment of missing data in clinical trials. N Engl J Med. 2012;367:1355–60.CrossRef Little RJ, D’agostino R, Cohen ML, Dickersin K, Emerson SS, Farrar JT, et al. The prevention and treatment of missing data in clinical trials. N Engl J Med. 2012;367:1355–60.CrossRef
38.
go back to reference Bottomley A, Pe M, Sloan J, Basch E, Bonnetain F, Calvert M, et al. Moving forward toward standardizing analysis of quality of life data in randomized cancer clinical trials. Clin Trials. 2018;15:624–30.CrossRef Bottomley A, Pe M, Sloan J, Basch E, Bonnetain F, Calvert M, et al. Moving forward toward standardizing analysis of quality of life data in randomized cancer clinical trials. Clin Trials. 2018;15:624–30.CrossRef
39.
go back to reference Bell ML, Fiero M, Horton NJ, Hsu C-H. Handling missing data in RCTs; a review of the top medical journals. BMC Med Res Methodol. 2014;14:118.CrossRef Bell ML, Fiero M, Horton NJ, Hsu C-H. Handling missing data in RCTs; a review of the top medical journals. BMC Med Res Methodol. 2014;14:118.CrossRef
Metadata
Title
Handling informative dropout in longitudinal analysis of health-related quality of life: application of three approaches to data from the esophageal cancer clinical trial PRODIGE 5/ACCORD 17
Authors
B. Cuer
C. Mollevi
A. Anota
E. Charton
B. Juzyna
T. Conroy
C. Touraine
Publication date
01-12-2020
Publisher
BioMed Central
Published in
BMC Medical Research Methodology / Issue 1/2020
Electronic ISSN: 1471-2288
DOI
https://doi.org/10.1186/s12874-020-01104-w

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