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首页> 外文期刊>Contemporary clinical trials >Making strides and meeting challenges in pediatric allogeneic hematopoietic cell transplantation clinical trials in the United States: Past, present and future
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Making strides and meeting challenges in pediatric allogeneic hematopoietic cell transplantation clinical trials in the United States: Past, present and future

机译:在美国小儿同种异体造血细胞移植临床试验中取得进展并迎接挑战:过去,现在和将来

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Over the past 20 years, the field of pediatric allogeneic hematopoietic cell transplantation has made ground-breaking strides in the successful treatment of patients with both malignant and non-malignant diseases. As the field advances, so does the need for high-quality studies including randomized controlled trials, aimed at answering clinically important questions about optimizing care and outcomes of children undergoing alloHCT. In an effort to actively address emerging clinical questions, three main cooperative groups in the U.S. have joined forces to develop and implement multiple clinical trials for pediatric alloHCT patients. These groups include the Blood and Marrow Transplant Clinical Trials Network, the Children's Oncology Group and the Pediatric Blood and Marrow Transplant Consortium. Though the field of stem cell transplantation continues to advance, conducting clinical trials in the pediatric population is a unique challenge and as a result, optimal outcomes have yet to be reached in this population. Because of the limited number of pediatric transplant patients at each institution in the U.S., trials aimed at answering important clinical questions still struggle to accrue acceptable numbers of patients in an appropriate amount of time and thus gathering statistically useful data has posed a challenge for the field. In an effort to mitigate some of the challenges associated with obtaining statistically and clinically meaningful information about pediatric alloHCT, the implementation of new cooperative group trials is active and ongoing. (C) 2015 Published by Elsevier Inc.
机译:在过去的20年中,小儿同种异体造血细胞移植领域在成功治疗恶性和非恶性疾病患者方面取得了突破性进展。随着该领域的发展,对包括随机对照试验在内的高质量研究的需求也在不断提高,这些研究旨在回答关于优化接受alloHCT的儿童的护理和结果的临床重要问题。为了积极解决新出现的临床问题,美国的三个主要合作组织已联合开发并实施了针对小儿同种异体HCT患者的多项临床试验。这些小组包括血液和骨髓移植临床试验网络,儿童肿瘤学小组以及小儿血液和骨髓移植联合会。尽管干细胞移植的领域不断发展,但在儿科人群中进行临床试验是一个独特的挑战,因此,该人群尚未达到最佳结果。由于美国各机构的小儿移植患者数量有限,旨在回答重要临床问题的试验仍难以在适当的时间内获得可接受数量的患者,因此收集统计学上有用的数据对该领域提出了挑战。为了缓解与获得有关儿科AlloHCT的统计和临床意义信息有关的一些挑战,正在积极开展新的合作组试验。 (C)2015年由Elsevier Inc.出版

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