Premaratne Gehan, McCarthy Maria, Tennant Michelle, Downie Peter, Hearps Stephen, De Luca Cinzia
University of Melbourne, Melbourne, VIC, Australia.
Children's Cancer Centre, The Royal Children's Hospital, Melbourne, VIC, Australia.
J Cancer Surviv. 2024 Dec 26. doi: 10.1007/s11764-024-01736-7.
Survival for childhood Acute Lymphoblastic Leukaemia (ALL) has surpassed 90%, making quality of survival an important endpoint in treatment outcomes. This study examined health-related quality of life (HRQoL) trajectories in early survivorship for patients post-ALL treatment compared with a matched group of healthy peers, and explored the association of individual factors (age, sex) and treatment intensity with HRQoL outcomes.
Eighty-three paediatric patients aged 4-16 years who recently completed treatment for ALL were recruited to the study, alongside 53 age- and sex-matched healthy children. All participants completed the self-report Pediatric Quality of Life Inventory (PedsQL) generic score scale at 3-, 15- and 27-months post-study enrolment.
Trajectory of overall HRQoL for the patient group declined over time, falling below clinical cutoffs at 27 months. Subscale trajectories differed between groups, with patients' emotional and social functioning negatively diverging relative to healthy peers, while school functioning remained consistently reduced. Children treated for ALL experienced significantly poorer HRQoL compared to healthy peers at 27 months post-treatment (p = 0.027, ES = - 0.47) with moderate effect sizes, reflecting lower social functioning (p = 0.044, ES = - 0.42) and school functioning (p = 0.011, ES = - 0.52). Age and sex were not associated with overall HRQoL at 27 months; however, younger age was associated with reduced emotional functioning in the standard treatment-intensity group.
HRQoL is impaired in children treated for ALL in early survivorship, particularly across social and school functioning domains. Screening using patient-reported outcomes is reliable at identifying young people at risk and has potential to guide psychosocial interventions in this early off-treatment period.
儿童急性淋巴细胞白血病(ALL)的生存率已超过90%,因此生存质量成为治疗结果的一个重要指标。本研究对比了一组配对的健康同龄人,考察了ALL治疗后患者早期生存阶段与健康相关的生活质量(HRQoL)轨迹,并探讨了个体因素(年龄、性别)和治疗强度与HRQoL结果之间的关联。
招募了83名4至16岁近期完成ALL治疗的儿科患者,以及53名年龄和性别匹配的健康儿童。所有参与者在研究入组后3个月、15个月和27个月完成了自我报告的儿童生活质量量表(PedsQL)通用评分量表。
患者组的总体HRQoL轨迹随时间下降,在27个月时降至临床临界值以下。各子量表轨迹在两组之间存在差异,患者的情感和社会功能相对于健康同龄人呈负向分化,而学校功能持续降低。与健康同龄人相比,ALL治疗后的儿童在治疗后27个月时的HRQoL明显更差(p = 0.027,ES = -0.47),效应量中等,反映出社会功能(p = 0.044,ES = -0.42)和学校功能(p = 0.011,ES = -0.52)较低。年龄和性别与27个月时的总体HRQoL无关;然而,在标准治疗强度组中,年龄较小与情感功能降低有关。
ALL治疗后的儿童在早期生存阶段的HRQoL受损,尤其是在社会和学校功能领域。使用患者报告结果进行筛查在识别有风险的年轻人方面是可靠的,并且有可能在这个早期治疗后阶段指导心理社会干预。