Application of FET-PET in Fusion With MRI in the Surgical Treatment and Postoperative Radiotherapy of Glioblastoma Multiforme - a Randomized, Blinded, Prospective Study
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 189
- 试验地点
- 2
- 主要终点
- Progression-free survival
研究概览
简要总结
Glioblastoma multiforme (GBM WHO IV) is the most common and aggressive primary brain tumor in adults, carrying a poor prognosis with a median survival of 12-16 months. The annual incidence is approximately 5 per 100,000 (roughly 600 cases annually in Poland), predominantly affecting individuals in their prime productive years. The standard of care consists of maximal safe resection followed by the Stupp protocol (60 Gy fractionated radiotherapy and temozolomide chemotherapy).
Routine surgical management relies on contrast-enhanced MRI. Gross total resection (GTR) is defined as the complete removal of the contrast-enhancing lesion. Although GTR improves progression-free survival (PFS) and overall survival (OS), local recurrence at the operative site occurs in up to 51% of patients within a year. This rapid regrowth is driven by glioblastoma stem cells infiltrating the surrounding non-enhancing brain tissue. Consequently, standard contrast-enhanced MRI lacks the sensitivity required to define true tumor boundaries for optimal patient outcomes.
To overcome this, positron emission tomography (PET-CT) using amino acid tracers like 18F-fluoroethyl-L-tyrosine (18F-FET) offers a promising alternative. Unlike 18-FDG, which is obscured by physiologically high glucose uptake in healthy brain tissue, 18F-FET provides high specificity and sensitivity for glial tumors. Crucially, studies show that MRI contrast enhancement overlaps with only 58% of the hypermetabolic area identified by 18F-FET. While "supramarginal" resections based on FLAIR MRI abnormalities (assumed to contain infiltrating stem cells) improve PFS by roughly 2 months, the FLAIR sequence cannot definitively distinguish active tumor infiltration from standard peritumoral edema.
This proposed experiment carries significant innovative value: it aims to use the fusion of 18F-FET PET and contrast-enhanced MRI to precisely guide both primary surgical resection and postoperative radiotherapy. By redefining the primary target volume to include the area of true biological tumor activity rather than just the MRI-enhancing mass (incorporating it into GTV, CTV, and PTV planning), the procedure directly targets residual glioblastoma stem cells. While PET has been evaluated for radiotherapy planning in recurrent GBM, high-quality data regarding its use for primary surgical planning is lacking. This study aims to fill that crucial gap in the literature.
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
- Double (Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 70 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Single macroscopic tumor focus with the appearance of glioblastoma multiforme on MRI with contrast - contrast-enhancing lesion, completely or with central necrosis, with surrounding edema.
- •No history of cancer in other organs. No suspicious lesions on X-ray of the chest and abdomen (CT with contrast).
- •No clinical suspicion of brain abscess - no meningeal symptoms, signs of neuroinfection, fever, elevated inflammatory parameters.
- •Primary tumor, without neurosurgical, radiotherapy or oncology intervention. Prior tumor biopsy is allowed.
- •Tumor eligible for surgical treatment - craniotomy and tumor resection.
- •Age ≥ 18 years but < 70 years old.
- •Quality of life assessment: KPS ≥
- •Informed patient consent to the study and proposed treatment.
- •No allergy to contrast agents used in PET and MRI.
- •No medical contraindications to neurosurgery - craniotomy and resection.
排除标准
- •Multifocal brain tumor.
- •Recurrence of glioblastoma multiforme.
- •Clinical or radiological suspicion of brain metastasis or brain abscess.
- •Postoperative histopathological diagnosis other than WHO grade IV glioblastoma.
- •Medical contraindications to any surgery under general anesthesia.
- •Pregnancy, breastfeeding.
- •Known allergy to gadolinium contrast or radiopharmaceutical tracing agent.
研究组 & 干预措施
Resection and radiotherapy according to the MRI & PET fusion
Surgical treatment and radiotherapy planned based on FET-PET and MRI+T1C fusion.
干预措施: MRI & PET fusion (Other)
Radiotherapy according to the MRI & PET fusion
Surgical treatment planned based on MRI+T1C study, radiotherapy planned based on FET-PET and MRI+T1C fusion.
干预措施: MRI & PET fusion (Other)
Radiotherapy according to the MRI & PET fusion
Surgical treatment planned based on MRI+T1C study, radiotherapy planned based on FET-PET and MRI+T1C fusion.
干预措施: MRI+T1C (Other)
Resection and radiotherapy according to the MRI
Surgical treatment and radiotherapy planned based on MRI+T1C.
干预措施: MRI+T1C (Other)
结局指标
主要结局
Progression-free survival
时间窗: 36 months post surgery
Overall survival
时间窗: 36 months post surgery
次要结局
- Volumetric assessment of the planned radiotherapy volume based on PET-MRI and MRI planning.(1 day before radiotherapy)
- Assessment of tumor volume (GTV) in MRI with contrast in relation to the tumor borders in PET-CT(1 day before radiotherapy)
- Long-term survival rate and prognostic factors (longer than 1 year from diagnosis).(36 months post surgery)
- Pattern of local recurrence based on postoperative PET-MRI. Assessment of the nature and location of local recurrence based on the postoperative SUV parameter MET-PET and MRI examination.(36 months post surgery)
- Assessment of quality of life related (SF-36 questionnaire) to the increase in the volume of the tumor undergoing treatment.(7 days post surgery, 1 day before and after radiotherapy)
- Pattern of local recurrence based on postoperative PET-MRI. Assessment of the nature and location of local recurrence based on the postoperative SUV parameter FET-PET and MRI examination.(36 months post surgery)
研究者
Kamil Krystkiewicz
Principal Investigator
Copernicus Memorial Hospital
