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临床试验/NCT01902576
NCT01902576进行中(未招募)不适用

Chronic GVHD Response Measures Validation

Fred Hutchinson Cancer Center2 个研究点 分布在 1 个国家目标入组 383 人开始时间: 2013年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
383
试验地点
2
主要终点
Develop and validate the Chronic GVHD-Activity Index (CGVHD-AI) as a measure of treatment response.

研究概览

简要总结

The purpose of this study is to develop and validate endpoint measures that can accurately determine whether patients are responding to treatment for chronic Graft-versus-Host Disease (GVHD). Hopefully, this will also lead to being better able to predict which patients will respond to what therapies.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
7 Years 至 99 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 7 years or older
  • Prior first allogeneic stem cell transplant, with any graft source, donor type, and GVHD prophylaxis.
  • Diagnosis of chronic GVHD according to the criteria of the diagnosis and scoring group of the NIH consensus conference (Patient must have at least one diagnostic manifestation of chronic GVHD or one distinctive manifestation with pathological confirmation of the diagnosis. Concurrent acute GVHD manifestations will be allowed as long as at least one classic chronic manifestation is present.)
  • Initiation of a new systemic treatment for chronic GVHD in the past 4 weeks or anticipated within the next 4 weeks. Systemic treatment is defined as any medication or intervention that has intended systemic effects, including extracorporeal photopheresis, regardless of prior lines of therapy or prior treatment with the agent(s). If a patient is restarting a treatment to which they were previously exposed, they must have been off of it for at least 4 weeks before restarting.
  • No evidence of persistent or progressive malignancy at the time of enrollment
  • Evaluation at the transplant center at the time of study enrollment, and agreement to be re-evaluated at the transplant center up to four subsequent times: at 3 months, 6 months, and 18 months after enrollment and once if another treatment is added for chronic GVHD.
  • Signed, informed consent

排除标准

  • Inability to comply with study procedures
  • Complete resolution of chronic GVHD at the time of enrollment (patient must have some measurable chronic GVHD activity)

结局指标

主要结局

Develop and validate the Chronic GVHD-Activity Index (CGVHD-AI) as a measure of treatment response.

时间窗: 18 months

This measure is intended to capture impairments caused by chronic GVHD. We expect that change in the CGVHD-AI could be used to measure treatment response because it will correlate with clinically significant changes reported by physicians and patients. The CGVHD-AI would be most appropriate for use in clinical trials where the goal is symptom relief and decreased disease activity.

次要结局

  • To develop and validate the Chronic GVHD Failure-Free Survival Score (CGVHD-FFS) as a predictor of failure-free survival.(18 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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