此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

NgFUS NIVO: NeuroNavigation-Guided Focused Ultrasound With Nivolumab in Relapsed and Progressive DMG and Other High Grade Brain Tumors

2026年9月8日 更新者:Children's National Research Institute

A Safety and Feasibility Study of NeuroNavigation-Guided Low Intensity Focused Ultrasound With Microbubbles to Enhance Nivolumab Delivery for the Treatment of Relapsed and Progressive Diffuse Midline Glioma and Other High Grade Brain Tumors

This is an open-label phase 1 safety and feasibility study evaluating a novel combination therapy for progressive and relapsed diffuse midline glioma (DMG) and other progressive and relapsed high-grade brain tumors. This study combines intravenous nivolumab therapy infused following transient blood-brain barrier opening (BBBO) using low-intensity focused ultrasound with microbubble (LIFU-MB) treatment using NeuroNavigation-Guided Focused Ultrasound (NgFUS).

There are two groups in this study:

  • Group A: Patients with relapsed or progressive diffuse midline glioma in the brainstem
  • Group B: Patients with relapsed or progressive high grade brain tumor that clinically require surgical resection

The primary outcome is to evaluate the safety and feasibility of 3 cycles of nivolumab with BBB disruption using NgFUS with microbubbles in pediatric patients with progressive or relapsed brainstem DMG or with high grade brain tumors after surgery. Secondary outcomes include preliminary efficacy and immunological effects.

研究概览

研究类型

介入性

注册 (估计的)

30

阶段

  • 阶段1

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

研究联系人备份

学习地点

    • District of Columbia
      • Washington D.C.、District of Columbia、美国、20010

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 孩子
  • 成人

接受健康志愿者

不

描述

Inclusion Criteria:

  • Age ≥ 3 and ≤ 25 years.
  • Diagnosis of brainstem DMG/DIPG or any high-grade brain tumor.

    • Group A: Relapsed or progressive brainstem DMG.
    • Group B: Relapsed or progressive high-grade intracranial brain tumor requiring surgical resection.
  • Lansky/Karnofsky rating ≥ 60.
  • Patients must have received at least one line of prior therapy upfront for their disease.
  • At least four weeks from radiation therapy, prior immunotherapy, or monoclonal antibody therapy.
  • At least 2 weeks from prior myelosuppressive chemotherapy and post nadir meeting organ function criteria.
  • At least 1 week or 5 half-lives (whichever is longer) from last targeted therapy.
  • If on steroids, stable or decreasing dose for at least 7 days prior to study entry and ≤ 0.4 mg/m2/day of dexamethasone or equivalent.
  • Stable or improving neurological status for 7 days prior to study entry.
  • Organ function:

    • Absolute Neutrophil Count (ANC) ≥750/μL.
    • Absolute Lymphocyte Count (ALC) >500/μL.
    • Platelets ≥75K, unsupported.
    • Coagulation studies: PT and PTT <1.5 ULN and INR (<1.5).
    • Bilirubin ≤1.5x upper limit of normal (ULN).
    • AST/ALT ≤5x ULN.
    • Serum creatinine within normal limits for age.
    • Pulse oximetry >93% on room air.
    • Ejection Fraction (EF) above institutional lower limit of normal (LLN).
  • For females of childbearing potential (FOCBP): negative pregnancy test within 7 days of study entry.
  • Patients of childbearing or child-fathering potential must agree to use contraceptive measures for at least 5 months following nivolumab infusion.
  • Patient or parent/guardian capable of providing informed consent.

Exclusion Criteria:

  • Symptoms and signs of increased intracranial pressure.
  • Patients with metallic ventricular peritoneal shunts. Subjects with nonmetallic VP shunts or similar will have a technical evaluation of the screening non-contrast CT scan of the head. During the mapping of the target area, if the technical NaviFUS specialist determines that the patient cannot be treated within the safety limits of the system, the patient will not be eligible and will be considered a screen failure.
  • Tumor presenting with the following imaging characteristics:

    • Evidence of uncal herniation.
    • Edema and/or mass effect that causes hydrocephalus.
    • Significant areas of necrosis within the tumor that the neurosurgeon feels cannot be avoided during the ultrasound sonication.
    • Evidence of a significant new hemorrhage. Area of microhemorrhage (defined as less than 5 mm in diameter) in the treatment area can be acceptable but requires the review of the neurosurgeon.
    • Containing calcifications in the focused ultrasound sonication beam path and system tools cannot tailor the treatment around these calcification spots.
    • Patients who are deemed to have overly bulky tumor by the PI of the study.
  • The sonication pathway to the tumor involves:

    • More than 30% of the skull area traversed by the sonication pathway is covered by scars, scalp disorders (e.g., eczema), or atrophy of the scalp.
    • Clips, or other non-MRI compatible metallic implanted objects in the skull or the brain, except for shunts.
  • Patients receiving anti-coagulant therapy, or medications known to increase risk of hemorrhage, (e.g., ASA, non-steroidal anti-inflammatory drugs [NSAIDs], statins). There is no required washout for eligibility assessment, but patients should be off agents for at least 3 days at the time of procedure or until 5 half-lives of the agent, whichever is longer.
  • History of a bleeding disorder, coagulopathy or with a history of clinically significant spontaneous tumor hemorrhage.
  • Cerebral or systemic vasculopathy, including intracranial thrombosis, vascular malformation, cerebral aneurysm, or vasculitis.
  • Immunosuppression (corticosteroids to prevent/treat brain edema are permitted).
  • Patients with uncontrolled HIV.
  • Active seizure disorder or epilepsy (clinically significant seizures despite medical treatment) within four weeks prior to first cycle/NaviFUS BBBO procedure captured by history.
  • Known sensitivity to gadolinium-based contrast agents.
  • Known sensitivity to Lumason® ultrasound contrast agent or known hypersensitivity to sulphur hexafluoride microsphere or its components, e.g., polyethylene glycol.
  • Patients unable to fit comfortably into the MRI scanner (generally >250 lbs.).
  • Evidence of cranial or systemic infection.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:非随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Group A: Patients with relapsed or progressive diffuse midline glioma in the brainstem
Patients with relapsed or progressive diffuse midline glioma in the brainstem, receiving nivolumab with NgFUS either every 2 weeks or every 4 weeks.
NeuroNavigation-Guided Focused Ultrasound, every 2 or 4 weeks for 3 cycles of 28 days
Lumason is a sulfur hexafluoride microsphere ultrasound contrast agent which will be used as a mechanical resonator. Lumason will be given in combination with NgFUS every 2 or 4 weeks for 3 cycles of 28 days.
Nivolumab is a monoclonal antibody targeting the immune checkpoint axis PD-1/PD-L1. Nivolumab will be given prior to NgFUS with microbubbles (Lumason) every 2 or 4 weeks for 3 cycles of 28 days.
实验性的:Group B: Patients with relapsed or progressive high grade brain tumors requiring surgical resection
Patients with relapsed or progressive high grade brain tumors that clinically require surgical resection, receiving one dose of NgFUS prior to surgery, and nivolumab with NgFUS every 4 weeks following recovery from surgery.
NeuroNavigation-Guided Focused Ultrasound, every 2 or 4 weeks for 3 cycles of 28 days
Lumason is a sulfur hexafluoride microsphere ultrasound contrast agent which will be used as a mechanical resonator. Lumason will be given in combination with NgFUS every 2 or 4 weeks for 3 cycles of 28 days.
Nivolumab is a monoclonal antibody targeting the immune checkpoint axis PD-1/PD-L1. Nivolumab will be given prior to NgFUS with microbubbles (Lumason) every 2 or 4 weeks for 3 cycles of 28 days.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Incidence of dose limiting toxicities (DLT) as assessed by CTCAE v6.0.
大体时间:First treatment through 28 days post-first treatment.
Safety will be evaluated by the incidence of DLTs. DLT is defined as toxicities which are at least possibly related to treatment and meeting protocol-specified criteria for grade, duration, severity, and/or delay of subsequent treatment cycles. If the overall toxicity rate exceeds protocol-specified criteria, enrollment will be halted and the study will be amended to modify the treatment plan.
First treatment through 28 days post-first treatment.
Percentage of patients completing at least two cycles of planned therapy
大体时间:Enrollment through end of Cycle 2 (each cycle is 28 days).
Treatment will be determined feasible if at least 80% of enrolled patients complete at least 2 cycles of planned therapy. Feasibility will be assessed separately for each cohort.
Enrollment through end of Cycle 2 (each cycle is 28 days).

次要结果测量

结果测量
措施说明
大体时间
Overall response assessment per RAPNO.
大体时间:From screening through 1 year post-final treatment.
Overall response assessment: complete response (CR), partial response (PR), minor response (MR), stable disease (SD), or progressive disease (PD) following treatment, will be assessed based on the Response Assessment in Pediatric Neuro-Oncology (RAPNO) scale.
From screening through 1 year post-final treatment.
Progression-free survival (PFS)
大体时间:From enrollment through up to 2 years post-final treatment.
PFS is defined as the interval of time between the date of protocol treatment initiation and the earliest date of documentation of progressive disease, or second malignancy or death (for any reason) for patients who fail, or to date of last contact or initiation of other therapy for patients who remain at risk of failure.
From enrollment through up to 2 years post-final treatment.
Overall survival (OS)
大体时间:From enrollment through up to 2 years post-final treatment.
OS post nivolumab infusion will be analyzed by the Kaplan-Meier method.
From enrollment through up to 2 years post-final treatment.

其他结果措施

结果测量
大体时间
Tissue expression of PD-1 and PD-L1
大体时间:From enrollment through immediately after surgery.
From enrollment through immediately after surgery.
Lymphocyte counts according to FUS area treated
大体时间:From enrollment through 3 months post-final treatment.
From enrollment through 3 months post-final treatment.
Immunologic correlates
大体时间:Pre- and post-procedure starting from enrollment through immediately after the final treatment (Cycle 3 Day 0 for Q4Week Group A and Group B, or Cycle 3 Day 14 for Q2Week Group A).
Pre- and post-procedure starting from enrollment through immediately after the final treatment (Cycle 3 Day 0 for Q4Week Group A and Group B, or Cycle 3 Day 14 for Q2Week Group A).
Immunohistochemistry for PD1/PDL1
大体时间:From enrollment through immediately after surgery.
From enrollment through immediately after surgery.
Immunostaining for lymphocytes
大体时间:From enrollment through immediately after surgery.
From enrollment through immediately after surgery.
Increase of areas (measured in percentage) of contrast enhancement on T1-gadolinium MRI sequences obtained immediately following BBB disruption.
大体时间:From enrollment through 36 hours after the final treatment (Cycle 3 Day 0 for Q4Week Group A and Group B, or Cycle 3 Day 14 for Q2Week Group A).
From enrollment through 36 hours after the final treatment (Cycle 3 Day 0 for Q4Week Group A and Group B, or Cycle 3 Day 14 for Q2Week Group A).

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年9月1日

初级完成 (估计的)

2030年12月1日

研究完成 (估计的)

2030年12月1日

研究注册日期

首次提交

2026年5月20日

首先提交符合 QC 标准的

2026年6月17日

首次发布 (实际的)

2026年6月24日

研究记录更新

最后更新发布 (实际的)

2026年9月9日

上次提交的符合 QC 标准的更新

2026年9月8日

最后验证

2026年9月1日

更多信息

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

订阅