Department of Epidemiology and Cancer Control, St Jude Children's Research Hospital, Memphis, Tennessee.
Department of Pharmaceutical Sciences, St Jude Children's Research Hospital, Memphis, Tennessee.
JAMA Oncol. 2016 Feb;2(2):201-8. doi: 10.1001/jamaoncol.2015.4398.
This study provides the first objective data documenting neurocognitive impairment in long-term survivors of childhood osteosarcoma.
To examine neurocognitive, neurobehavioral, emotional, and quality-of-life outcomes in long-term survivors of childhood osteosarcoma.
DESIGN, SETTING, AND PARTICIPANTS: Cross-sectional cohort study at an academic research hospital, with prospective treatment and chronic health predictors. Outcome data were collected from June 2008 to August 2014. Data analysis was completed in April 2015. Survivors of osteosarcoma recruited from the St Jude Lifetime Cohort Study were compared with community controls.
Neurocognitive function, neurobehavioral symptoms, emotional distress, and quality of life. Outcomes were examined in relation to pharmacokinetic indices of methotrexate exposure and current chronic health conditions, which were assessed through medical examination and coded according to Common Terminology Criteria for Adverse Events, Version 4.03.
Eighty survivors of osteosarcoma (mean [SD] age, 38.9 [7.6] years; time since diagnosis, 24.7 [6.6] years; 42% female) were compared with 39 community controls (age, 39.0 [11.7] years; 56% female). Survivors demonstrated lower mean scores in reading skills (-0.21 [95% CI, -0.32 to -0.10] vs 0.05 [95% CI, -0.13 to 0.23]; P = .01), attention (-0.78 [95% CI, -1.32 to -0.24] vs 0.24 [95% CI, -0.07 to 0.55]; P = .002), memory (-0.24 [95% CI, -0.48 to 0] vs 0.27 [95% CI, -0.08 to 0.62]; P = .01), and processing speed (-0.15 [95% CI, -0.35 to 0.05] vs 0.74 [95% CI, 0.44 to 1.03]; P < .001). Results of pharmacokinetic analysis showed that high-dose methotrexate maximum plasma concentration (estimate = 0; P = .48), median clearance (estimate = -0.11; P = .76), and median/cumulative exposure (estimate = 0; P = .45) were not associated with neurocognitive outcomes. Any grade 3 or 4 Common Terminology Criteria for Adverse Events cardiac, pulmonary, or endocrine condition was associated with poorer memory (t = 2.93; P = .006) and slower processing speed (t = 3.03; P = .002). Survivor-reported poor general health was associated with decreased sustained attention (estimate = 0.24; P = .05) and processing speed (estimate = 0.34; P = .005).
Long-term survivors of osteosarcoma are at risk for neurocognitive impairment, which is related to current chronic health conditions and not to original treatment with high-dose methotrexate. Prospective longitudinal studies are needed to identify onset and progression of impairment to inform optimal interventions.
本研究提供了首份客观数据,记录了骨肉瘤儿童长期幸存者的神经认知障碍。
研究骨肉瘤长期幸存者的神经认知、神经行为、情绪和生活质量结果。
设计、地点和参与者:在学术研究医院进行的横断面队列研究,具有前瞻性治疗和慢性健康预测因素。2008 年 6 月至 2014 年 8 月期间收集了结果数据。2015 年 4 月完成了数据分析。从圣裘德终身队列研究中招募的骨肉瘤幸存者与社区对照进行了比较。
神经认知功能、神经行为症状、情绪困扰和生活质量。通过阅读技能(-0.21 [95%置信区间,-0.32 至-0.10] vs 0.05 [95%置信区间,-0.13 至 0.23];P = 0.01)、注意力(-0.78 [95%置信区间,-1.32 至-0.24] vs 0.24 [95%置信区间,-0.07 至 0.55];P = 0.002)、记忆(-0.24 [95%置信区间,-0.48 至 0] vs 0.27 [95%置信区间,-0.08 至 0.62];P = 0.01)和处理速度(-0.15 [95%置信区间,-0.35 至 0.05] vs 0.74 [95%置信区间,0.44 至 1.03];P < 0.001)来评估神经认知功能。药代动力学分析结果表明,高剂量甲氨蝶呤最大血浆浓度(估计值= 0;P = 0.48)、中位数清除率(估计值=-0.11;P = 0.76)和中位数/累积暴露(估计值= 0;P = 0.45)与神经认知结果无关。任何等级 3 或 4 的常见不良事件术语标准心脏、肺部或内分泌疾病与较差的记忆(t = 2.93;P = 0.006)和较慢的处理速度(t = 3.03;P = 0.002)相关。幸存者报告的一般健康状况较差与持续注意力(估计值= 0.24;P = 0.05)和处理速度(估计值= 0.34;P = 0.005)降低有关。
骨肉瘤的长期幸存者有神经认知障碍的风险,这与当前的慢性健康状况有关,而与高剂量甲氨蝶呤的原始治疗无关。需要前瞻性纵向研究来确定损伤的发病和进展,以提供最佳干预措施。