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Extraorally delivered photobiomodulation therapy for prevention of oropharyngeal mucositis in pediatric patients undergoing hematopoietic cell transplantation

机译:地理递送了光致考试治疗,用于预防口咽粘膜肌炎,患儿造血细胞移植

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Background: Oral mucositis (OM) is a painful consequence of myeloablative hematopoietic cell transplantation (HCT). Extraorally delivered photobiomodulation therapy (PBMT) is a promising novel intervention for the prevention of OM in children. Objectives: With funding from an NIDCR R34 planning grant, the objectives of this study are 1) to model the dosimetry of external PBMT and the optimal device parameters for the planned clinical trial, and 2) to plan and design a placebo-controlled Phase 2 multicenter clinical trial to determine whether extraorally delivered PBMT can reduce the duration of severe OM in children, with intent for implementation under subsequent U01 funding. Methods: External PBMT dosimetry will be evaluated using pediatric head and neck MRI studies to obtain serial measurements of different tissues that will then be used to develop a sophisticated computational model. We plan to conduct a placebo-controlled Phase 2 multicenter clinical trial in which patients 4 to 21 years of age will be randomized 1:1:1 to receive external PBMT dose 1x, external PBMT dose 2x, or sham PBMT starting from conditioning, daily until day +20 post-HCT. Significance: Extraorally delivered PBMT is a feasible, potentially efficacious intervention that could improve the quality of life for all children undergoing myeloablative HCT. The planned Phase 2 study, based on rigorous dose modeling and with detailed attention to uniform delivery of therapy and OM assessments, will provide critical efficacy data and the potential basis for a subsequent definitive Phase 3 trial. Grant Support: NIDCR R34 DE025908-01.
机译:背景:口腔粘液炎(OM)是髓鞘造血细胞移植(HCT)的痛苦后果。地理递送的光生物调节治疗(PBMT)是一种有助于预防儿童OM的新型干预。目标:从NIDCR R34规划补助金提供资金,本研究的目标为1)以模拟外部PBMT的剂量测定和计划的临床试验的最佳设备参数,以及2)计划和设计安慰剂控制阶段2多中心临床试验,以确定异常交付的PBMT是否可以减少儿童严重肿块的持续时间,意图在随后的U01资金下实施。方法:将使用小儿头和颈部MRI研究评估外部PBMT剂量测定法,以获得不同组织的串行测量,然后将用于开发复杂的计算模型。我们计划进行安慰剂对照的2阶段多中心临床试验,其中4至21岁的患者将被随机1:1:1接受外部PBMT剂量1X,外部PBMT剂量2x,或从调节,每日起作用的假PBMT直到第+20天后HCT。意义:外来交付的PBMT是一种可行的,潜在有效的干预措施,可以提高所有蒙脱土HCT的儿童的生活质量。根据严格的剂量建模和详细关注治疗和OM评估的详细注意,计划第2阶段研究将为随后的最终阶段3试验提供关键的疗效数据和潜在的基础。授予支持:NIDCR R34 DE025908-01。

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