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Psychosocial Functioning After Pediatric Bone Sarcoma: Generic and Survivor-Specific Outcomes in Adolescent and Young Adult Patients

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Abstract

Background: Pediatric bone sarcoma patients and survivors may experience psychosocial challenges related to childhood cancer after their intensive, body-altering treatment. This cross-sectional study aimed to evaluate generic and survivor-specific psychosocial outcomes in a national cohort of pediatric bone sarcoma patients and survivors, and to explore associations between these outcomes. Methods: Patients treated for pediatric bone sarcoma, at least 2 years post-diagnosis, completed age-appropriate Pediatric Quality of Life Inventory (PedsQL) and PROMIS measures (generic outcomes). Patients ≥18 years additionally completed the impact of cancer–childhood survivor (IOC-CS) (survivor-specific outcomes). Generic psychosocial outcomes of patients were compared with age- and sex-specific Dutch normative data using one-sample t-tests. Linear regression analyses, adjusted for age and sex, examined associations between generic and survivor-specific outcomes. Results: In total, 139 patients participated (45% female). Mean age was 20.4 years (SD = 5.5) and mean time since end of treatment was 7.0 years (SD = 5.2). Patients scored significantly worse than normative values on cognitive functioning, pain interference, and health-related quality of life. In other generic domains, such as depressive symptoms or anxiety, patients scored comparably to or better than normative values. Survivor-specific outcomes were most positive in the socializing domain and most negative in the thinking and memory domain. Approximately 20% reported moderate-to-severe negative impact in at least one survivor-specific domain. Conclusion: Overall, pediatric bone sarcoma patients demonstrated psychosocial outcomes comparable to or more favorable than normative values. However, specific domains showed worse outcomes. In addition, a substantial subgroup experienced moderate-to-severe negative impacts of childhood cancer. This highlights the importance of monitoring psychosocial functioning and, where indicated, targeted interventions to address challenges.

Original languageEnglish
Article numbere70487
JournalPediatric Blood and Cancer
Volume73
Issue number9
DOIs
Publication statusPublished - Sept 2026

Keywords

  • childhood cancer
  • pediatric oncology
  • psycho-oncology
  • psychosocial functioning
  • quality of life
  • supportive care

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