18F-AGX PET for Evaluation of Vorasidenib Response and Tumor Metabolic Changes in Low-grade IDH-Mutant Glioma
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 10
- 试验地点
- 1
- 主要终点
- Change in Tumor Metabolic Activity Assessed by 18F-AGX PET
研究概览
简要总结
The goal of this prospective, single-arm, open-label clinical trial is to evaluate whether 18F-AGX PET imaging can be used to assess early treatment response and metabolic changes in adult patients with recurrent or residual WHO 2021 grade 2-3 IDH-mutant diffuse glioma receiving Vorasidenib therapy.
IDH-mutant diffuse gliomas often show slow tumor growth, making early treatment response difficult to evaluate using conventional structural imaging such as magnetic resonance imaging (MRI). Clinical endpoints such as progression-free survival (PFS) and overall survival (OS) typically require long follow-up periods to detect treatment effects. Therefore, the development of sensitive and noninvasive imaging methods for early evaluation of therapeutic response is needed.
This study aims to determine whether metabolic changes detected by 18F-AGX PET during Vorasidenib treatment are associated with tumor structural changes and clinical outcomes.
The main questions it aims to answer are:
- Whether early changes in tumor metabolic activity measured by 18F-AGX PET, including percentage change in maximum tumor-to-background ratio (TBRmax), are associated with changes in tumor growth rate (TGR) measured by MRI during treatment.
- Whether early metabolic response detected by 18F-AGX PET imaging after initiation of Vorasidenib treatment can predict subsequent disease progression or tumor growth dynamics.
Participants enrolled in this study will receive oral Vorasidenib once daily for 12 treatment cycles (28 days per cycle), with dosing based on body weight.
Participants will:
- Undergo baseline MRI and 18F-AGX PET imaging following surgery for recurrent or residual disease.
- Receive oral Vorasidenib continuously for 12 cycles.
- Undergo MRI scans at baseline and during treatment cycles 1, 2, 3, 6, 9, and 12 to assess structural tumor changes.
- Undergo 18F-AGX PET/CT scans at baseline and during treatment cycles 1, 2, 3, 6, and 12 to assess metabolic tumor activity.
- Provide serial blood samples for laboratory safety monitoring, including hematologic and biochemical testing.
- Undergo magnetic resonance spectroscopy (MRS) to quantify intratumoral 2-hydroxyglutarate (2-HG) levels as an indicator of IDH mutation-associated metabolic activity.
Participants will be followed for imaging-based disease progression using RANO criteria and for treatment-related adverse events during the study period.
This study will evaluate the feasibility of using 18F-AGX PET imaging as a noninvasive imaging biomarker for early response assessment in IDH-mutant diffuse glioma patients receiving targeted IDH inhibition therapy with Vorasidenib.
详细描述
Diffuse gliomas harboring mutations in isocitrate dehydrogenase (IDH1 or IDH2) represent a biologically distinct subgroup of central nervous system tumors characterized by the accumulation of the oncometabolite D-2-hydroxyglutarate (2-HG). Mutant IDH enzymes catalyze the reduction of α-ketoglutarate to 2-HG, leading to widespread epigenetic dysregulation, impaired cellular differentiation, and altered tumor metabolism. These metabolic alterations are considered key drivers of glioma tumorigenesis and progression.
Vorasidenib is an oral, brain-penetrant, dual inhibitor of mutant IDH1 and IDH2 enzymes that has demonstrated clinical activity in patients with IDH-mutant diffuse glioma. By selectively inhibiting mutant IDH enzymatic activity, Vorasidenib reduces intratumoral 2-HG production and is expected to modify tumor metabolic processes. However, due to the relatively slow growth kinetics of IDH-mutant gliomas, conventional structural imaging techniques such as magnetic resonance imaging (MRI) may not detect treatment-related changes in tumor size during the early phases of therapy. As a result, reliance on morphologic imaging alone may delay the identification of therapeutic response or disease progression.
Metabolic imaging approaches have the potential to provide earlier indicators of biological treatment effects. Magnetic resonance spectroscopy (MRS) has been used to quantify intratumoral 2-HG concentrations in vivo as a surrogate of mutant IDH activity. While MRS-based measurements may reflect pharmacodynamic effects of IDH inhibition, its sensitivity and spatial resolution may limit its utility for longitudinal monitoring of treatment response in clinical practice.
Positron emission tomography (PET) imaging using radiolabeled tracers enables the quantitative assessment of tumor metabolism and has been shown to detect treatment-related metabolic changes that precede morphologic alterations observed on MRI. Amino acid PET tracers such as 18F-FET and 18F-FDOPA have demonstrated the ability to identify early metabolic responses in glioma patients undergoing systemic therapy, with metabolic response correlating with clinical outcomes in some studies.
18F-AGX is a novel PET radiotracer designed to selectively bind to IDH-mutant glioma cells. Preclinical studies have demonstrated that 18F-AGX crosses the blood-brain barrier and exhibits increased uptake in IDH-mutant glioma models compared with IDH wild-type tumors. In experimental settings, treatment with Vorasidenib has been associated with reductions in tracer uptake that parallel decreases in intratumoral 2-HG levels, suggesting that 18F-AGX PET imaging may serve as a noninvasive indicator of target engagement and metabolic response.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
盲法说明
This is an open-label study. Participants, care providers, and investigators are aware of treatment assignment. Imaging-based outcome assessments are performed by an independent central review committee blinded to clinical information and treatment response.
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
- •Histologically or molecularly confirmed WHO 2021 grade 2 or 3 IDH1/2-mutant diffuse glioma with recurrent or residual disease
- •At least one measurable non-enhancing lesion (≥1 cm × ≥1 cm) on postoperative T2/FLAIR MRI
- •Eligible for Vorasidenib treatment
- •Age ≥18 years
- •Karnofsky Performance Status (KPS) score ≥80
- •Adequate hematologic function
- •Adequate renal function
- •Adequate hepatic function
- •Ability to provide written informed consent
排除标准
- •Prior treatment with radiotherapy, chemotherapy, or IDH inhibitors
- •Known contraindications to Vorasidenib
- •Contraindications to PET/CT imaging
- •Uncontrolled hyperglycemia
- •Pregnancy or breastfeeding
- •Inability to undergo repeated intravenous injections
- •Known hypersensitivity to imaging agents or study-related medications
- •Use of strong CYP1A2 inhibitors or CYP2C19 or CYP3A substrates with narrow therapeutic index
- •Any serious comorbid condition that may interfere with study participation or safety
研究组 & 干预措施
Vorasidenib Treatment with 18F-AGX PET Assessment
Participants receive oral Vorasidenib once daily for up to 12 treatment cycles (28 days per cycle). Serial 18F-AGX PET imaging and MRI assessments are performed during treatment to evaluate metabolic and structural tumor changes associated with IDH-targeted therapy.
干预措施: Oral Vorasidenib administered once daily for up to 12 treatment cycles (28 days per cycle) as IDH-targeted therapy in participants with recurrent or residual IDH-mutant diffuse glioma. (Drug)
结局指标
主要结局
Change in Tumor Metabolic Activity Assessed by 18F-AGX PET
时间窗: Up to 12 treatment cycles (approximately 12 months)
Percentage change from baseline in maximum tumor-to-background ratio (TBRmax) measured by 18F-AGX PET imaging during Vorasidenib treatment.
次要结局
- Tumor Growth Rate Assessed by MRI(From baseline to the end of Cycle 12 (each cycle is 28 days; approximately 12 months))
- Diagnostic Accuracy of 18F-AGX PET for IDH Mutation Detection(At baseline imaging assessment)
- Incidence of Treatment-Related Adverse Events(From the first dose of Vorasidenib to the end of Cycle 12 (each cycle is 28 days; approximately 12 months))
研究者
Zhifeng Shi
Clinical Professor, Associate Chief Physician, Deputy Director of Huashan Clinical Research Institute, Huashan Hospital, Fudan University
Huashan Hospital