LONG-TERM FOLLOW-UP OF CHILDREN WITH ACUTE LEUKEMIA WHO UNDERWENT SCT
LONG-TERM FOLLOW-UP OF CHILDREN WITH ACUTE LEUKEMIA WHO UNDERWENT SCT
批准号:
7375887
负责人:
KEVIN S BAKER
金额:
$0.39万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-12-01 至 2006-11-30
中文摘要
该子项目是利用NIH/NCRR资助的中心赠款提供的资源的许多研究子项目之一。子项目和研究者(PI)可能从另一个NIH来源获得主要资金,因此可以在其他CRISP条目中表示。所列机构为中心,不一定是研究者所在机构。儿童期干细胞移植与许多长期并发症有关,包括内分泌异常,神经认知困难,学习成绩差,骨质疏松症和心肺功能异常。很少有大规模的研究评估这些迟发效应在白血病治疗儿童中的发生率,特别是对小于3岁的白血病移植儿童的长期并发症知之甚少。我们研究的主要目的是更好地确定婴儿和幼儿期SCT的长期并发症。我们能够在明尼苏达大学进行这样的研究,因为该机构已经进行了大量的儿科干细胞移植,特别是白血病儿童,以及该队列的随访时间(现在超过20年)。到目前为止,还没有一项研究以前瞻性、随机化的方式系统评价SCT幸存者。该方法将消除以下偏倚:(1)基于保险覆盖范围的可用性选择受试者,以支付长期随访的费用,(2)患者或家庭返回该机构进行持续随访的财务资源,(3)以及发生过晚期效应的患者优先参与的潜在选择偏倚。这将是一项队列研究,研究对象为在Minesota大学接受SCT的ALL或AML儿童,年龄小于10岁,并且至少存活1年。潜在受试者将包括明尼苏达大学SCT数据库中现有的受试者总数,其中(1)(2)移植时<10岁的所有或AML患者和(3)SCT后存活>或= 1年且目前处于缓解状态的受试者。研究者将联系受试者,解释研究并提供参与。所有参与费用(包括差旅和住宿)将由研究承担,因此参与者的时间将是其参与的唯一“成本”。这项研究将在明尼苏达大学的综合临床研究中心进行。受试者将接受全面的神经心理学和神经内分泌/代谢评价。GCRC将提供检查空间、护理和实验室绘图支持以及DEXA扫描。体格检查时,将由护理人员医生测量身高、体重、坦纳分期(青春期发育)和体重/身高。实验室评估将包括内分泌功能的测量,包括甲状腺功能(T4和TSH)和性腺功能[FSH、LH、骨代谢的代谢参数(吸收/形成),包括钙、镁、磷、骨钙素、骨特异性碱性磷酸酶、尿N-端肽和其他代谢参数,包括血脂、空腹胰岛素和葡萄糖,将进行肾功能(BUN/肌酸酐,UA)和肝功能测试的标准测量。所有受试者将接受DEXA扫描以评估骨矿物质密度,以及骨龄X射线(对于女性>9和<19,男性>10和<18)。在完成体格检查和血液检查后,所有受试者将接受由同一儿科神经心理学家进行的适合年龄的神经心理学评估。用于本研究的神经心理学测试的所有组成部分都是标准化的,年龄特异性的(并且在不同年龄之间具有可比性),并将评估广泛的神经认知和功能领域。将要求父母(或患者,如果目前年龄大于10岁)填写一份问卷,以评估任何移植相关医学晚期效应的发生率和生活质量评估(City of Hope BMT QOL、SF-36或儿童健康问卷,取决于受试者年龄)。
英文摘要
This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. Stem cell transplantation in childhood has been associated with many long-term complications in cluding endocrine abnormalities, neurocognitive difficulties, poor school performance, osteoporosis, and cardiopulmonary abnormalities. Few large-scale studies have evaluated the incidence of these late effects in children treated for leukemia, and specifically very little is known about the long-term complications in children transplanted for leukemia at less than three years of age. The primary objective of our research will be to better define the long-term complications of SCT in infancy and very young childhood. We are uniquely able to perform such a study here at the University of Minnesota given the large number of pediatric stem cell transplants that have been performed at this institution, particularly for children wih leukemia, and the length of follow-up that is available on this cohort (now over 20 year). To date, there has not been a study that has systematically evaluated SCT survivors in a prospective, randomized fashion. This method will eliminate the bias of (1) subject selection based upon the availability of insurance coverage to cover the costs of long-term follow-up, (2) financial resources of a patient of family to return to this institution for ongoing follow-up, (3) and the potential selection bias of preferential participation by patients that have experienced late effects. This will be a cohort study of children with ALL or AML who a SCT at the University of Minesota when they were less than ten years of age, and have survived at least one year. Potential subjects will include the total existing number of subjects in the University of Minnesota SCT database with (1) All or AML who were (2) <10 years at the time of transplant and (3) have survived > or = 1 year post-SCT currently in remission. Subjects will be contacted by the investigators to explain the study and offer participation. All costs of participation, including travel and lodging will be borne by the study so that participant time will be the only "cost" of their participation. The study will take place in the General Clinical Research Center at the University of Minnesota. Subjects will undergo full neuropsychological and neuroendocrine/metabolic evaluation. The GCRC would provide exam space, nursing and lab draw support, and DEXA scanning. Measurement of height, weight, Tanner Staging (pubertal development) and body weight/height will be obtained at the time of the physical examination by nursing staff physicians. Laboratory assessment will in clude measures of endocrinologica functions including thyroid function (T4 and TSH) and gonadal function [FSH, LH, Metabolic parameters of bone metabolism (resorption/formation) including calcium, magnesium, phosphorus, osteocalcin, bone specific alkaline phosphatase, urinary N-telopeptide, and additional metabolic parameters including lipid profile, fasting insulin and glucose, standard measures of renal function (BUN/creatinine, UA) and liver function tests would be performed. All subjects will undergo DEXA scanning for evaluation of bone mineral density, as well as bone age x-rays (for females>9 and <19, males >10 and <18). After completion of physical exam and blood work, all subjects will undergo an age appropriate neuropsychological evaluation administeres by the same pediatric neuropsychologist. All components of this neuropsychological testing to be utilized for this study are standardized, age specific (and comparable across different ages) and will assess a wide range of neurocognitive and functional domains. Parents (or patients if presently older than 10 years of age) will be asked to complete a questionnaire that will assess the occurrence of any transplant related medical late effects and an assessment of quality of life (City of Hope BMT QOL, SF-36, or Child Health Questionnaire, depending on subject age).
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