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Risk and Protective Factors of Psychosocial Functioning in Survivors of Childhood Cancer: Results of the DCCSS-LATER Study

  • Anne Maas*
  • , Heleen Maurice-Stam
  • , DCCSS-LATER Study Group
  • , E. A.M. Feijen
  • , Jop C. Teepen
  • , Alied M. van der Aa-van Delden
  • , Nina Streefkerk
  • , Eline van Dulmen-den Broeder
  • , Wim J.E. Tissing
  • , Jacqueline J. Loonen
  • , Helena J.H. van der Pal
  • , Andrica C.H. de Vries
  • , Marry M. van den Heuvel-Eibrink
  • , Cécile Ronckers
  • , Sebastian Neggers
  • , Dorine Bresters
  • , Marloes Louwerens
  • , Birgitta A.B. Versluys
  • , Margriet van der Heiden-van der Loo
  • , Leontien C.M. Kremer
  • Martha Grootenhuis
*Corresponding author for this work
  • Princess Máxima Center for Pediatric Oncology
  • Amsterdam UMC
  • University of Groningen
  • Radboud University Medical Center
  • Johannes Gutenberg University Mainz
  • Leiden University
  • Utrecht University
  • University of Amsterdam

Research output: Contribution to journalArticleAcademicpeer-review

3 Citations (Scopus)
65 Downloads (Pure)

Abstract

Objective: 

This study examines the association between psychosocial risk and protective factors and a wide range of psychosocial outcomes including emotional, social, cognitive, and physical domains in childhood cancer survivors (CCS). 

Methods: 

CCS from the Dutch Childhood Cancer Survivor Study (DCCSS)-LATER cohort (diagnosed 1963–2001) part 2 (age ≥ 18 years, diagnosed < 18 years, ≥ 5 years since diagnosis) completed questionnaires on psychosocial risk and protective factors (Benefit and Burden Scale, Illness Cognition Questionnaire, Rosenberg Self-Esteem Scale, and Impact of Cancer Scale), and psychosocial outcomes (Hospital Anxiety and Depression Scale, Self-Rating Scale for Post-Traumatic Stress Disorder, TNO-AZL Questionnaire for Adult Health-Related Quality of Life, and Short Form-36). Associations were assessed with regression analysis, adjusting for attained age, sex, number of health conditions, and time since diagnosis, while correcting for multiple testing (p < 0.004). 

Results: 

A total of 1382 CCS participated, all diagnosed ≥ 15 years ago. The mean age of participating CCS was 36 years, and 51% were female. Perceived benefit and burden, acceptance, and helplessness, self-esteem and social support were associated with the psychosocial outcomes. In the models including all psychosocial factors, most associations with psychosocial outcomes were seen for self-esteem (10×), and perceived burden (9×). Self-esteem (all β ≤ 0.47) and perceived burden (all β ≤ 0.38) demonstrated strongest associations of medium/large size. 

Conclusions: 

Perceptions of childhood cancer, illness cognitions, self-esteem, and social support play a role in explaining psychosocial functioning in CCS, outweighing the influence of socio-demographic and medical variables. Addressing negative perceptions and reducing feelings of helplessness, while promoting acceptance, self-esteem, and social support, could provide intervention targets for CCS who encounter psychosocial challenges.

Original languageEnglish
Article numbere9313
JournalPsycho-Oncology
Volume33
Issue number10
DOIs
Publication statusPublished - Oct 2024

Bibliographical note

Publisher Copyright:
© 2024 The Author(s). Psycho-Oncology published by John Wiley & Sons Ltd.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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