TY - JOUR
T1 - Risk and Protective Factors of Psychosocial Functioning in Survivors of Childhood Cancer
T2 - Results of the DCCSS-LATER Study
AU - Maas, Anne
AU - Maurice-Stam, Heleen
AU - Feijen, E. A.M.
AU - Teepen, Jop C.
AU - van der Aa-van Delden, Alied M.
AU - Streefkerk, Nina
AU - van Dulmen-den Broeder, Eline
AU - Tissing, Wim J.E.
AU - Loonen, Jacqueline J.
AU - van der Pal, Helena J.H.
AU - de Vries, Andrica C.H.
AU - van den Heuvel-Eibrink, Marry M.
AU - Ronckers, Cécile
AU - Neggers, Sebastian
AU - Bresters, Dorine
AU - Louwerens, Marloes
AU - Versluys, Birgitta A.B.
AU - van der Heiden-van der Loo, Margriet
AU - Kremer, Leontien C.M.
AU - Grootenhuis, Martha
N1 - Publisher Copyright:
© 2024 The Author(s). Psycho-Oncology published by John Wiley & Sons Ltd.
PY - 2024/10
Y1 - 2024/10
N2 - 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.
AB - 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.
KW - childhood cancer survivors
KW - health-related quality of life
KW - illness cognitions
KW - illness perceptions
KW - psycho-oncology
KW - psychosocial functioning
KW - self-esteem
KW - social support
UR - http://www.scopus.com/inward/record.url?scp=85205527071&partnerID=8YFLogxK
U2 - 10.1002/pon.9313
DO - 10.1002/pon.9313
M3 - Article
C2 - 39358839
AN - SCOPUS:85205527071
SN - 1057-9249
VL - 33
JO - Psycho-oncology
JF - Psycho-oncology
IS - 10
M1 - e9313
ER -