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临床试验/NCT06448286
NCT06448286尚未招募3 期

PH Weighted Chemical Exchange Saturation Transfer Based Surgical Resections of Glioblastoma

Jonsson Comprehensive Cancer Center1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2026年12月1日最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
尚未招募
入组人数
60
试验地点
1
主要终点
Progression free survival

研究概览

简要总结

This phase III trial compares pH weighted chemical exchange saturation transfer (CEST) magnetic resonance imaging (MRI)-based surgical resections to standard of care surgical resections for the treatment of patients with glioblastoma. Standard of care therapy for glioblastoma is surgery to remove tumor tissue that enhances on standard MRI imaging, however, it has been shown that significant tumor burden exists in the region around the tumor tissue that does not enhance with standard MRI. MRI is a procedure in which radio waves and a powerful magnet linked to a computer are used to create detailed pictures of areas inside the body. These pictures can show the difference between normal and tumor tissue. CEST MRI is a technique that uses differences in the tissue environment, like protein concentration or intracellular pH, to generate contrast differences. CEST MRI may identify tumor tissue that does not enhance with standard of care MRI. PH weighted CEST MRI based surgical resection may be more effective compared to standard of care surgical resection in treating patients with glioblastoma.

详细描述

PRIMARY OBJECTIVE:

I. To assess the efficacy of potential of hydrogen (pH) sensitive MRI based resections of glioblastoma.

SECONDARY OBJECTIVE:

I. To find surgical and adjuvant therapies to treat infiltrating glioblastoma cells.

OUTLINE: Patients are randomized to 1 of 2 groups.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Investigator, Outcomes Assessor)

盲法说明

The patient, investigators and research staff will be blinded.

入排标准

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

入选标准

  • Male or female ≥ 18 years of age
  • Documentation of a newly diagnosed World Health Organization (WHO) grade IV glioblastoma as evidenced by clinical features and imaging data
  • Written informed consent (and assent when applicable) obtained from subject or subject's legal representative and ability for subject to comply with the requirements of the study

排除标准

  • Male or female < 18 years of age
  • Presence of a condition or abnormality that in the opinion of the Investigator would compromise the safety of the patient or the quality of the data
  • Not medically cleared for surgery
  • Previous treatment (any chemotherapy, molecular therapy, immunotherapy, or radiation therapy)

研究组 & 干预措施

Group I (standard of care surgical resection)

Active Comparator

Patients undergo surgical resection with standard intraoperative guidance using contrast-enhanced MRI. Patients also undergo post operative standard of care radiation therapy over 30 fractions and receive standard of care temozolomide PO for 6 weeks. Additionally, patients undergo MRI during follow up.

干预措施: Contrast-enhanced Magnetic Resonance Imaging (Procedure)

Group II (CEST MRI based surgical resection)

Experimental

Patients undergo surgical resection with intraoperative guidance using CEST MRI. Patients also undergo post operative standard of care radiation therapy over 30 fractions and receive standard of care temozolomide PO for 6 weeks. Additionally, patients undergo MRI during follow up.

干预措施: Chemical Exchange Saturation Transfer Magnetic Resonance Imaging (Procedure)

Group I (standard of care surgical resection)

Active Comparator

Patients undergo surgical resection with standard intraoperative guidance using contrast-enhanced MRI. Patients also undergo post operative standard of care radiation therapy over 30 fractions and receive standard of care temozolomide PO for 6 weeks. Additionally, patients undergo MRI during follow up.

干预措施: Magnetic Resonance Imaging (Procedure)

Group II (CEST MRI based surgical resection)

Experimental

Patients undergo surgical resection with intraoperative guidance using CEST MRI. Patients also undergo post operative standard of care radiation therapy over 30 fractions and receive standard of care temozolomide PO for 6 weeks. Additionally, patients undergo MRI during follow up.

干预措施: Magnetic Resonance Imaging (Procedure)

Group II (CEST MRI based surgical resection)

Experimental

Patients undergo surgical resection with intraoperative guidance using CEST MRI. Patients also undergo post operative standard of care radiation therapy over 30 fractions and receive standard of care temozolomide PO for 6 weeks. Additionally, patients undergo MRI during follow up.

干预措施: Radiation Therapy (Radiation)

Group I (standard of care surgical resection)

Active Comparator

Patients undergo surgical resection with standard intraoperative guidance using contrast-enhanced MRI. Patients also undergo post operative standard of care radiation therapy over 30 fractions and receive standard of care temozolomide PO for 6 weeks. Additionally, patients undergo MRI during follow up.

干预措施: Radiation Therapy (Radiation)

Group I (standard of care surgical resection)

Active Comparator

Patients undergo surgical resection with standard intraoperative guidance using contrast-enhanced MRI. Patients also undergo post operative standard of care radiation therapy over 30 fractions and receive standard of care temozolomide PO for 6 weeks. Additionally, patients undergo MRI during follow up.

干预措施: Surgical Procedure (Procedure)

Group II (CEST MRI based surgical resection)

Experimental

Patients undergo surgical resection with intraoperative guidance using CEST MRI. Patients also undergo post operative standard of care radiation therapy over 30 fractions and receive standard of care temozolomide PO for 6 weeks. Additionally, patients undergo MRI during follow up.

干预措施: Surgical Procedure (Procedure)

Group I (standard of care surgical resection)

Active Comparator

Patients undergo surgical resection with standard intraoperative guidance using contrast-enhanced MRI. Patients also undergo post operative standard of care radiation therapy over 30 fractions and receive standard of care temozolomide PO for 6 weeks. Additionally, patients undergo MRI during follow up.

干预措施: Temozolomide (Drug)

Group II (CEST MRI based surgical resection)

Experimental

Patients undergo surgical resection with intraoperative guidance using CEST MRI. Patients also undergo post operative standard of care radiation therapy over 30 fractions and receive standard of care temozolomide PO for 6 weeks. Additionally, patients undergo MRI during follow up.

干预措施: Temozolomide (Drug)

结局指标

主要结局

Progression free survival

时间窗: Up to 2 years

Multivariate cox and log rank tests will be used to compare progression free survival.

次要结局

  • Overall survival(Up to 2 years)
  • Surgical complication rate(Up to 2 years)
  • Quality of life(Up to 2 years)
  • Quality of life: Karnofsky Performance Status(Up to 2 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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