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Joint modelling with competing risks of dropout for longitudinal analysis of health-related quality of life in cancer clinical trials

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  • معلومة اضافية
    • Contributors:
      Institut régional de Cancérologie de Montpellier (ICM); Institut de Recherche en Cancérologie de Montpellier (IRCM - U1194 Inserm - UM); CRLCC Val d'Aurelle - Paul Lamarque-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM); Plateforme Nationale Qualité de vie et Cancer; Institut de Cancérologie de Lorraine - Alexis Vautrin Nancy (UNICANCER/ICL); UNICANCER; Adaptation, mesure et évaluation en santé. Approches interdisciplinaires (APEMAC); Université de Lorraine (UL); Institut Desbrest de santé publique (IDESP); Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM)
    • بيانات النشر:
      HAL CCSD
      Springer Verlag
    • الموضوع:
      2022
    • Collection:
      Université de Montpellier: HAL
    • نبذة مختصرة :
      International audience ; Purpose: Health-related quality of life (HRQoL) is an important endpoint in cancer clinical trials. Analysis of HRQoL longitudinal data is plagued by missing data, notably due to dropout. Joint models are increasingly receiving attention for modelling longitudinal outcomes and the time-to-dropout. However, dropout can be informative or non-informative depending on the cause.Methods We propose using a joint model that includes a competing risks sub-model for the cause-specific time-to-dropout. We compared a competing risks joint model (CR JM) that distinguishes between two causes of dropout with a standard joint model (SJM) that treats all the dropouts equally. First, we applied the CR JM and SJM to data from 267 patients with advanced oesophageal cancer from the randomized clinical trial PRODIGE 5/ACCORD 17 to analyse HRQoL data in the presence of dropouts unrelated and related to a clinical event. Then, we compared the models using a simulation study.Results We showed that the CR JM performed as well as the SJM in situations where the risk of dropout was the same whatever the cause. In the presence of both informative and non-informative dropouts, only the SJM estimations were biased, impacting the HRQoL estimated parameters Conclusion The systematic collection of the reasons for dropout in clinical trials would facilitate the use of CR JMs, which could be a satisfactory approach to analysing HRQoL data in presence of both informative and non-informative dropout.Trial registration: This study is registered with ClinicalTrials.gov, number NCT00861094.
    • Relation:
      info:eu-repo/semantics/altIdentifier/pmid/34817733; hal-03467977; https://hal.umontpellier.fr/hal-03467977; https://hal.umontpellier.fr/hal-03467977/document; https://hal.umontpellier.fr/hal-03467977/file/MANUSCRIPT_postprint_all.pdf; PUBMED: 34817733; WOS: 000722098800001
    • الرقم المعرف:
      10.1007/s11136-021-03040-8
    • Rights:
      info:eu-repo/semantics/OpenAccess
    • الرقم المعرف:
      edsbas.B3B02747