학술논문

A vulnerable age group: the impact of cancer on the psychosocial well-being of young adult childhood cancer survivors
Original Article
Document Type
Academic Journal
Source
Supportive Care in Cancer. August 2021, Vol. 29 Issue 8, p4751, 11 p.
Subject
Psychological aspects
Diseases
Social aspects
Analysis
Depression (Mood disorder) -- Psychological aspects -- Analysis -- Social aspects
Childhood cancer -- Psychological aspects -- Analysis -- Social aspects
Cancer survivors -- Social aspects -- Psychological aspects -- Analysis
Youth -- Analysis -- Social aspects -- Psychological aspects
Cancer research -- Social aspects -- Psychological aspects -- Analysis
Fatigue -- Social aspects -- Analysis -- Psychological aspects
Medical care quality -- Analysis -- Social aspects -- Psychological aspects
Oncology, Experimental -- Social aspects -- Psychological aspects -- Analysis
Depression, Mental -- Psychological aspects -- Analysis -- Social aspects
Teenagers -- Analysis -- Social aspects -- Psychological aspects
Medical care -- Quality management
Cancer in children -- Psychological aspects -- Analysis -- Social aspects
Cancer -- Research
Language
English
ISSN
0941-4355
Abstract
Author(s): L. M. E. van Erp [sup.1], H. Maurice-Stam [sup.1], L. C. M. Kremer [sup.1] [sup.2], W. J. E. Tissing [sup.1] [sup.3], H. J. H. van der Pal [sup.1], A. [...]
Purpose This study aimed to increase our understanding of the psychosocial well-being of young adult childhood cancer survivors (YACCS) as well as the positive and negative impacts of cancer. Methods YACCS (aged 18-30, diagnosed [less than or equal to] 18, time since diagnosis [greater than or equal to] 5 years) cross-sectionally filled out the 'Pediatric Quality of Life Inventory Young Adults' (PedsQL-YA), 'Hospital Anxiety and Depression Scale' (HADS), and 'Checklist Individual Strengths' (CIS-20R) to measure fatigue and survivor-specific 'Impact of Cancer - Childhood Survivors' (IOC-CS), which measures the long-term impact of childhood cancer in several domains. Descriptive statistics (IOC-CS), logistic regression (HADS, CIS-20R), and ANOVA (PedsQL-YA, HADS, CIS-20R) were performed. Associations between positive and negative impacts of childhood cancer and psychosocial outcomes were examined with linear regression analyses. Results YACCS (N = 151, 61.6% female, mean age 24.1 ± 3.6, mean time since diagnosis 13.6 ± 3.8) reported lower HRQOL (- .4 [less than or equal to] d [less than or equal to] - .5, p [less than or equal to] .001) and more anxiety (d = .4, p [less than or equal to] .001), depression (d = .4, p [less than or equal to] .01), and fatigue (.3 [less than or equal to] d [less than or equal to] .5, p [less than or equal to] .001) than young adults from the general Dutch population. They were at an increased risk of experiencing (sub)clinical anxiety (OR = 1.8, p = .017). YACCS reported more impact on scales representing a positive rather than negative impact of CC. Various domains of impact of childhood cancer were related to psychosocial outcomes, especially 'Life Challenges' (HRQOL [beta] = - .18, anxiety [beta] = .36, depression [beta] = .29) and 'Body & Health' (HRQOL [beta] = .27, anxiety [beta] = - .25, depression [beta] = - .26, fatigue [beta] = - .47). Conclusion YACCS are vulnerable to psychosocial difficulties, but they also experience positive long-term impacts of childhood cancer. Positive and negative impacts of childhood cancer were associated with psychosocial outcomes in YACCS. Screening of psychosocial outcomes and offering targeted interventions are necessary to optimize psychosocial long-term follow-up care for YACCS.