TY - JOUR
T1 - Psychosocial Functioning After Pediatric Bone Sarcoma
T2 - Generic and Survivor-Specific Outcomes in Adolescent and Young Adult Patients
AU - van der Hoek, Hinke
AU - Maurice-Stam, Heleen
AU - Beek, Laura R.
AU - van Dijk, Jennifer
AU - Langemeijer, Marjolein E.M.
AU - Slooff-Lentink, Relinde W.
AU - van der Aa-van Delden, Alied M.
AU - Westerweel, Anne
AU - van Gorp, Marloes
AU - Schreuder, Hendrik W.B.
AU - Haveman, Lianne M.
AU - Bekkering, W. Peter
AU - Tigelaar, Leonie G.
AU - Merks, Johannes H.M.
AU - Grootenhuis, Martha A.
N1 - Publisher Copyright:
© 2026 The Author(s). Pediatric Blood & Cancer published by Wiley Periodicals LLC.
PY - 2026/9
Y1 - 2026/9
N2 - 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.
AB - 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.
KW - childhood cancer
KW - pediatric oncology
KW - psycho-oncology
KW - psychosocial functioning
KW - quality of life
KW - supportive care
UR - https://www.scopus.com/pages/publications/105046215936
U2 - 10.1002/1545-5017.70487
DO - 10.1002/1545-5017.70487
M3 - Article
AN - SCOPUS:105046215936
SN - 1545-5009
VL - 73
JO - Pediatric Blood and Cancer
JF - Pediatric Blood and Cancer
IS - 9
M1 - e70487
ER -