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临床试验/NCT01688401
NCT01688401已完成1 期

Intra-arterial Chemotherapy for the Treatment of Progressive Diffuse Intrinsic Pontine Gliomas (DIPG).

Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins1 个研究点 分布在 1 个国家目标入组 3 人开始时间: 2013年3月8日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
3
试验地点
1
主要终点
Technical safety as determined by number of participants with toxicity

研究概览

简要总结

The goal of this pilot study is to determine if intra-arterial (IA) chemotherapy is safe in the treatment of progressive diffuse intrinsic pontine gliomas (DIPG). IA administration of the chemotherapeutic agent enhances the regional distribution of the drug, thereby increasing the local delivered dose while minimizing systemic toxicity. It also provides a treatment option for these patients at the time of tumor recurrence.

详细描述

Delivering the chemotherapeutic agent directly to the tumor via the arterial system avoids the complications and adverse events associated with toxicity from systemic chemotherapy.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

年龄范围
1 Month 至 17 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Pediatric patients of all ages with progressive DIPG.
  • Consensus following presentation of the case at the multidisciplinary Pediatric Neuro-Oncology conference, which includes participation of neuro-oncology, neurosurgery, radiation oncology, interventional neuroradiology and neurology.

排除标准

  • Documented hypercoagulable disorders or vasculopathies
  • INR value more than a Grade 1 toxicity by CTCAE v 4.0 criteria (>1 - 1.5 x ULN; >1 - 1.5 times above baseline if on anticoagulation).
  • APTT value more than a Grade 1 toxicity by CTCAE v 4.0 criteria (>ULN - 1.5 x ULN).
  • Platelets less than 50 x 103/mm3
  • Absolute neutrophil count less than 500/ mm3
  • Pregnancy
  • Documented severe allergic reaction to IV iodinated contrast, specifically bronchospasm and anaphylaxis.

研究组 & 干预措施

IA melphalan

Experimental

IA melphalan is administered via the basilar artery.

干预措施: Melphalan hydrochloride (Drug)

结局指标

主要结局

Technical safety as determined by number of participants with toxicity

时间窗: 60 days

Number of participants with grades 3-5 intracranial hemorrhage, grades 3-5 stroke, as defined by the Nervous system disorder CTCAE, and requirement of blood transfusion.

次要结局

  • Long-term Efficacy as assessed by progression free survival(2 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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