Mitchell Hannah-Rose, Lu Xiaomin, Myers Regina M, Sung Lillian, Balsamo Lyn M, Carroll William L, Raetz Elizabeth, Loh Mignon L, Mattano Leonard A, Winick Naomi J, Devidas Meenakshi, Hunger Stephen P, Maloney Kelly, Kadan-Lottick Nina S
Department of Pediatric Hematology & Oncology, Yale University School of Medicine, New Haven, CT.
Department of Biostatistics, College of Public Health and Health Professions, University of Florida, Gainsville, FL.
Int J Cancer. 2016 Jan 15;138(2):332-9. doi: 10.1002/ijc.29708. Epub 2015 Sep 3.
Standard risk acute lymphoblastic leukemia (SR-ALL) has high cure rates, but requires 2-3 years of therapy. We aimed to (i) prospectively evaluate health-related quality of life (HRQOL) during and after SR-ALL therapy, and (ii) identify associated predictors. Parents of 160 SR-ALL patients enrolled on Children's Oncology Group (COG) therapeutic trial AALL0331 at 31 sites completed the Pediatric Quality of Life Inventory (PedsQL) 4.0 Generic Core Scales (physical, emotional and social functioning) and Family Assessment Device-General Functioning (FAD-GF) at 1, 6 and 12 months after diagnosis, and 3 months post-therapy. Mean PedsQL scores in physical, emotional and social functioning were impaired 1 month after diagnosis but steadily improved. Three months post-therapy, impaired physical and social functioning was observed in 27.8 and 25.8% of patients, respectively. In repeated-measures analysis, problematic family functioning predicted emotional (OR = 1.85, 95% CI 1.03-3.34) and social (OR = 1.99, 95% CI 1.21-3.27) impairment. Larger household size was associated with social impairment (OR = 1.21, 95% CI 1.02-1.45). Adverse neurological event(s) during therapy predicted post-therapy physical (OR = 5.17, 95% CI 1.61-16.63) and social (OR = 8.17, 95% CI 1.19-56.16) impairment. HRQOL 1 month after diagnosis was not predictive of HRQOL 3 months after therapy completion. In conclusion, children with SR-ALL experience considerable impairment in HRQOL at the end of induction, but rapidly improve. However, many still experience physical and social impairment 3 months post-therapy, suggesting a role for continued family and physical functioning support. Longer follow-up is needed to determine if post-therapy deficits change over time.
标准风险急性淋巴细胞白血病(SR-ALL)的治愈率很高,但需要2至3年的治疗。我们旨在:(i)前瞻性评估SR-ALL治疗期间及之后与健康相关的生活质量(HRQOL),以及(ii)确定相关预测因素。160名参加儿童肿瘤学组(COG)31个地点的AALL0331治疗试验的SR-ALL患者的父母在诊断后1、6和12个月以及治疗后3个月完成了儿童生活质量量表(PedsQL)4.0通用核心量表(身体、情感和社会功能)以及家庭评估量表-总体功能(FAD-GF)。诊断后1个月,身体、情感和社会功能方面的PedsQL平均得分受损,但稳步改善。治疗后3个月,分别有27.8%和25.8%的患者出现身体和社会功能受损。在重复测量分析中,有问题的家庭功能预示着情感(比值比[OR]=1.85,95%置信区间[CI]1.03-3.34)和社会(OR=1.99,95%CI 1.21-3.27)功能受损。家庭规模较大与社会功能受损相关(OR=1.21,95%CI 1.02-1.45)。治疗期间的不良神经事件预示着治疗后身体(OR=5.17,95%CI 1.61-16.63)和社会(OR=8.17,95%CI 1.19-56.16)功能受损。诊断后1个月的HRQOL不能预测治疗完成后3个月的HRQOL。总之,SR-ALL儿童在诱导治疗结束时HRQOL有相当大的受损,但改善迅速。然而,许多患者在治疗后3个月仍有身体和社会功能受损,这表明持续的家庭和身体功能支持有作用。需要更长时间的随访来确定治疗后缺陷是否随时间变化。