跳至主要内容
临床试验/NCT07219199
NCT07219199尚未招募不适用

Intraoperative Quantification of Residual IDH1-mutant Tumor Cells Via Ultra-Rapid Droplet Digital PCR

NYU Langone Health1 个研究点 分布在 1 个国家目标入组 105 人开始时间: 2027年8月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
105
试验地点
1
主要终点
Progression-Free Survival (PFS)

研究概览

简要总结

This is a single-site, single-arm, prospective, interventional cohort study using intraoperative ultra-rapid droplet digital polymerase chain reaction (UR- ddPCR) to assess residual IDH1-mutant tumor at the end of surgical resection and, if positive, guide additional resection in real-time.

研究设计

研究类型
干预性
分配方式
不适用
干预模型
单组
主要目的
诊断
盲法
开放(无盲法)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • Age ≥ 18 years at the time of consent (any sex)
  • Newly diagnosed diffuse glioma with either (a) radiographic features consistent with IDH-mutant glioma or (b) prior molecular confirmation of an IDH mutation
  • Scheduled for tumor tissue biopsy or surgical resection at NYU Langone Health

排除标准

  • Active hepatitis C virus (HCV) infection or suspected/confirmed prion disease (e.g., Creutzfeldt-Jakob disease), as documented in the medical record or by the treating physician, due to biosafety and tissue- handling restrictions

研究组 & 干预措施

UR-ddPCR During Tumor Biopsy/Resection Procedure

Experimental

During the participant's tumor biopsy or resection, the neurosurgeon will perform maximal safe resection, as per standard clinical practice, and allocate nine tissue specimens (three from the core of the tumor and six from the tumor-brain interface) for UR-ddPCR testing. If both core and tumor-brain interface samples test positive and further removal is judged safe, the neurosurgeon may perform additional resection and obtain final specimens from the positive sites before concluding the surgery. Up to 15 tissue specimens may be collected and tested during the procedure. Postoperative care and clinical follow-up will proceed per standard of care.

干预措施: UR-ddPCR (Device)

结局指标

主要结局

Progression-Free Survival (PFS)

时间窗: Up to Year 3 Post-Procedure

PFS is defined as the time from surgery to the time of the first MRI demonstrating radiographic progression (using Response Assessment in Neuro-Oncology \[RANO\] criteria) or death due to any cause (whichever occurs earlier).

次要结局

  • Residual Tumor Volume(Postoperative Day 1 (POD1))
  • Overall Survival (OS)(Up to Year 3 Post-Procedure)
  • Radiographic PFS(Month 6 Post-Procedure, Month 12 Post-Procedure, Month 24 Post-Procedure, Month 36 Post-Procedure)
  • Time to Radiographic Recurrence(Up to Year 3 Post-Procedure)
  • Percent Change in Mutant Allele Fraction (MAF)(Post-Operative Day 0 (POD0), post-additional resection of tumor-brain interface samples (Up to Year 3))

研究者

申办方类型
其他
责任方
申办方

研究点 (1)

Loading locations...

标识符

NCT 编号
NCT07219199
其他研究编号
Pending-IDE G250266

日期

首次提交
(11个月前)
首次发布
(11个月前)
主要完成日期
(5年后)
研究完成日期
(5年后)
最近核实
(29天前)
最近更新
(昨天)

监管与共享

FDA 监管药物
否
FDA 监管器械
是
个体参与者数据共享计划
UNDECIDED
是否有结果
否

相似试验