Badve Chaitra, Nirappel Abraham, Lo Simon, Orringer Daniel A, Olson Jeffrey J
University Hospitals Cleveland Medical Center, Cleveland, USA.
Department of Radiology, Case Western Reserve University School of Medicine, Cleveland, OH, USA.
J Neurooncol. 2025 May 8. doi: 10.1007/s11060-025-05043-8.
Adult patients with suspected or histologically proven WHO Grade II diffuse glioma. QUESTION 1: In adult patients with suspected or histologically proven WHO Grade II diffuse glioma, do advanced MRI techniques using magnetic resonance spectroscopy, perfusion weighted imaging or diffusion weighted imaging provide superior assessment of tumor grade, margins, progression, treatment-related effects, and prognosis compared to standard neuroimaging?
Level II: The use of diffusion imaging and dynamic susceptibility contrast (DSC), dynamic contrast enhancement (DCE) and arterial spin labeling (ASL) sequences are suggested to differentiate WHO Grade II diffuse glioma from higher grade gliomas when this is not accomplished by T2 weighted and pre- and post-gadolinium contrast enhanced T1 weighted imaging.
The use of diffusion and perfusion is suggested for obtaining information in genomics, prognosis, and post treatment monitoring when this information would be of value to the clinician and is not obtained through other methods.
The use of MR Spectroscopy is suggested to differentiate WHO Grade II diffuse glioma from higher grade gliomas when this is not accomplished by standard MRI, perfusion and diffusion techniques and when such information would be of value to the clinician. QUESTION 2: In adult patients with suspected or histologically proven WHO Grade II diffuse glioma, does molecular imaging using amino acid PET tracers provide superior assessment of tumor grade, margins, progression, treatment-related effects, and prognosis compared to standard neuroimaging?
Level III: If not already evident by MRI studies, the addition of amino acid PET with FET and FDOPA as a tracer is suggested to help determine if a brain lesion is a low grade glioma or high grade glioma.
If the standard clinical prognostic parameters are unclear and novel PET tracers are available, the clinician may consider FET to assist in determination of prognosis in an individual with grade II diffuse glioma.
Clinicians may use FDOPA PET in addition to MRI if additional information is required for detection of tumor progression.
疑似或经组织学证实为世界卫生组织(WHO)二级弥漫性胶质瘤的成年患者。
问题1:在疑似或经组织学证实为WHO二级弥漫性胶质瘤的成年患者中,与标准神经影像学检查相比,使用磁共振波谱、灌注加权成像或扩散加权成像的先进磁共振成像(MRI)技术在肿瘤分级、边界、进展、治疗相关效应及预后评估方面是否更具优势?
当T2加权成像以及钆剂增强前后的T1加权成像无法鉴别WHO二级弥漫性胶质瘤与高级别胶质瘤时,建议使用扩散成像和动态磁敏感对比(DSC)、动态对比增强(DCE)及动脉自旋标记(ASL)序列进行鉴别。
当扩散成像和灌注成像所提供的信息对临床医生有价值且无法通过其他方法获取时,建议使用扩散成像和灌注成像来获取基因组学、预后及治疗后监测方面的信息。
当标准MRI、灌注成像和扩散成像技术无法鉴别WHO二级弥漫性胶质瘤与高级别胶质瘤,且此类信息对临床医生有价值时,建议使用磁共振波谱进行鉴别。
问题2:在疑似或经组织学证实为WHO二级弥漫性胶质瘤的成年患者中,与标准神经影像学检查相比,使用氨基酸正电子发射断层扫描(PET)示踪剂的分子成像在肿瘤分级、边界、进展、治疗相关效应及预后评估方面是否更具优势?
如果MRI检查结果尚不明确,建议加做以氟代乙基酪氨酸(FET)和氟代多巴(FDOPA)为示踪剂的氨基酸PET检查,以帮助确定脑部病变是低级别胶质瘤还是高级别胶质瘤。
如果标准临床预后参数不明确且有新型PET示踪剂可用,临床医生可考虑使用FET协助判断II级弥漫性胶质瘤患者的预后。
如果检测肿瘤进展需要更多信息,临床医生除MRI外还可使用FDOPA PET。