Hematopoietic Cell Therapy for Young Adults with Severe Sickle Cell Disease

患有严重镰状细胞病的年轻人的造血细胞疗法

• 批准号: 8514705
• 负责人: Lakshmanan Krishnamurti
• 金额: $ 15.48万
• 依托单位: UNIVERSITY OF PITTSBURGH AT PITTSBURGH
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-09-01 至 2014-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8514705
• 关键词: Address; Adult; Age; Age-Years; Anemia; Antithymoglobulin; Appearance; Bone Marrow Transplantation; Busulfan; Cardiac; Caring; Cell Therapy; Cessation of life; Child; Childhood; Chimerism; Chronic; Clinical; Clinical Trials; Comprehensive Health Care; Cooley' s anemia; Data; Development; Disease; Disease Management; Disease Progression; Disease-Free Survival; Donor Selection; Eligibility Determination; Enrollment; Ensure; Erythrocyte Transfusion; Event; Frequencies; HLA Antigens; Health; Healthcare; Hematopoiesis; Hematopoietic; Impairment; Individual; Infection; Informed Consent; Inherited; Institutes; Investigation; Kidney Failure; Life; Light; Lung; Manuals; Marrow; Measurement; Measures; Medical; Monitor; Myeloproliferative disease; Natural History; Nature; Neonatal Screening; Neuraxis; Organ; Outcome; Pain; Patients; Pilot Projects; Premature Mortality; Preparation; Prophylactic treatment; Provider; Pulmonary Hypertension; Quality of life; Recruitment Activity; Regimen; Renal function; Research Design; Research Personnel; Role; Safety; Sample Size; Siblings; Sickle Cell; Sickle Cell Anemia; Stroke; Supportive care; Symptoms; System; Techniques; Testing; Therapeutic; Toxic effect; Transplantation; abstracting; arm; chronic pain; cohort; comparative; comparative trial; conditioning; demographics; design; electronic data; experience; fludarabine; graft vs host disease; hematopoietic cell transplantation; high risk; hydroxyurea; improved; leukocyte antigen typing; operation; premature; prevent; prospective; pulmonary function; sickling; statistics; trial comparing; young adult

DESCRIPTION (provided by applicant): Abstract Supportive health care measures instituted during childhood successfully prevent serious infections and many other life-threatening complications of sickle cell disease (SCD), resulting in improved survival to adulthood. This has, in part, shifted the demographics of SCD to include a growing proportion of young adults with chronic health impairments. While hematopoietic cell transplantation (HCT) has curative potential, very few individuals with SCD are treated by HCT, due in part to the toxicity of this treatment. Recently, advances in Human Leukocyte Antigen (HLA) typing techniques and supportive care have improved outcomes of HCT, particularly after unrelated donor HCT. A conditioning regimen of Busulfan, Fludarabine and anti-thymocyte globulin has a reduced toxicity profile and appears effective in HCT from unrelated donors in adults who have advanced myeloid malignancies and thalassemia major. We have organized an interdisciplinary group of transplant investigators and adult sickle cell providers to test the hypothesis that HCT from an HLA-identical sibling or unrelated marrow donor is safe and effective in young adults with severe SCD. We propose to test this hypothesis in a pilot investigation, which will also serve as a central planning mechanism for designing, organizing and launching a large parallel cohort clinical trial in which transplantation and supportive treatment for adults with severe SCD will be compared. Thus, we propose to investigate HCT in adults with severe sickle cell disease by the following specific aims: 1. Determine the feasibility and tolerability of HCT in young adults with severe sickle cell disease. 2. Measure the impact of donor hematopoiesis on end-organ function and define the sample size and clinical endpoints of a larger comparative clinical trial. If successfully planned and initiated, the proposed comparative clinical trial would be the first to compare HCT and supportive care for SCD, and could broaden the therapeutic opportunities for adults with severe SCD.

描述（由申请人提供）：摘要在儿童时期采取的支持性医疗保健措施成功地预防了镰状细胞病（SCD）的严重感染和许多其他危及生命的并发症，从而提高了成年后的生存率。这在一定程度上改变了SCD的人口统计数据，包括越来越多的患有慢性健康障碍的年轻人。虽然造血细胞移植（HCT）具有治愈潜力，但很少有SCD患者接受HCT治疗，部分原因是这种治疗的毒性。最近，人类白细胞抗原（HLA）分型技术和支持性治疗的进步改善了HCT的结果，特别是在无关供体HCT后。白消安，氟达拉滨和抗胸腺细胞球蛋白的预处理方案具有降低的毒性特征，并且在患有晚期骨髓恶性肿瘤和重型地中海贫血的成人中的无关供体的HCT中似乎有效。我们组织了一个由移植研究者和成人镰状细胞提供者组成的跨学科小组，以检验来自HLA相同的兄弟姐妹或无关骨髓供体的HCT在患有严重SCD的年轻人中安全有效的假设。我们建议在一项试点研究中检验这一假设，该研究也将作为设计、组织和启动一项大型平行队列临床试验的中央规划机制，在该试验中，将对严重SCD成人的移植和支持治疗进行比较。因此，我们建议通过以下具体目标来研究严重镰状细胞病成人的HCT：1。确定HCT在患有严重镰状细胞病的年轻人中的可行性和耐受性。2.测量供体造血对终末器官功能的影响，并确定更大规模比较临床试验的样本量和临床终点。如果成功计划和启动，拟议的比较临床试验将是第一个比较HCT和SCD支持治疗的试验，并可以拓宽患有严重SCD的成人的治疗机会。