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Impact of iMRI on the Extent of Resection in Patients With Newly Diagnosed Glioblastomas

Impact of iMRI on the Extent of Resection in Patients With Newly Diagnosed Glioblastomas - A Prospective Multicenter Parallel Group Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02379572
Enrollment
315
Registered
2015-03-05
Start date
2015-06-30
Completion date
2021-07-01
Last updated
2021-10-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Glioblastoma

Keywords

5-ALA, Intraoperative MRI, Extent of resection

Brief summary

Standard treatment of glioblastomas (GBMs) consists of microsurgical resection followed by concomitant chemoradiation. The extent of resection is one of the most important prognostic factors with significant influence on the survival of patients. State of the art technique to achieve the most radical resection possible in conventional surgery is fluorescence-guidance with 5-aminolevulinic acid (5-ALA). If available, intraoperative MRI (iMRI)-guided tumor resection enables an intraoperative resection control and subsequent continuation of surgery if contrast enhancing tumor remnants are found. Therefore a more radical resection and longer survival of patients might be possible. To date no comparison of these two leading technologies for GBM-surgery is available to identify the best surgical therapy of this fatal disease and to justify significant healthcare-economic differences between both technologies. Goal of this study is to assess the value of iMRI guidance in the resection of GBMs in comparison to conventional 5-ALA microsurgery. Primary endpoint is the number of total resections (no residual contrast enhancement) in the postoperative MRI (T1+CM within 48 hours after surgery) in each group. Secondary endpoints are perioperative clinical data, progression free survival, patients' clinical condition and overall survival. The study design was chosen to be a parallel-group approach to compare iMRI and 5-ALA centers (n=13) to exclude possible bias which might be found by randomizing patients within individual iMRI centers and to have surgeons with the most experience possible in use of each respective technology.

Interventions

DEVICEiMRI-guided surgery

For iMRI-guided glioma resections the surgery can be paused and a direct intraoperative resection control is possible by performing an intraoperative MRI scan. If residual tumor is found, the resection might be continued.

DRUG5-ALA-guided surgery

For 5-ALA guided glioma resections patients have to drink 100ml of a solution with 5-Aminolevulinic acid 4-6 hours before surgery. Intraoperatively the light source of the surgical microscope can be switched to a certain wave length to enable fluorescence of the glioma cells, which helps resecting the tumor as radical as possible.

Sponsors

University Hospital Tuebingen
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. In MRI suspected primary singular untreated GBM 2. Planned total resection of the tumor according to the surgeon 3. Patient ≥18 years, ≤80 years 4. Preoperative KPS ≥ 60%, American Society of Anesthesiologists (ASA) score 1 and 2 5. Patients' informed consent

Exclusion criteria

1. Tumors of the midline, basal ganglia, cerebellum, brain stem, eloquent areas 2. Multifocal glioblastoma 3. Substantial (\>50%), non-contrast enhancing tumor areas suggesting low-grade glioma with malignant transformation 4. Contraindications to MRI 5. Inability to give consent because of language barrier or dysphasia 6. Histological diagnosis other than Glioblastoma multiforme WHO °IV 7. Increased risk of thrombosis (e.g. Factor V Leiden) 8. Pregnancy or breast feeding 9. Hypersensibility for 5-ALA oder porphyrins 10. Acute or chronic Porphyria 11. Renal insufficiency 12. Hepatic insufficiency 13. High likelihood of inability to receive adjuvant therapy

Design outcomes

Primary

MeasureTime frameDescription
Complete resections in the postoperative MRI (T1+/-CM) within 48 hours after surgery48 hourCompleteness of resection in the postoperative MRI within 48h after surgery. Blinded analysis by an independent radiologist.

Secondary

MeasureTime frameDescription
Patients' clinical condition (KPS)preoperative (day before surgery), 1 week, 3Months, 6Months, 9Months, 12Months after surgery-KPS clinical scoring
Patients' clinical condition (NIHSS)preoperative (day before surgery), 1 week, 3Months, 6Months, 9Months, 12Months after surgery-NIHSS stroke score
Patients' clinical condition (QoL)preoperative (day before surgery), 1 week, 3Months, 6Months, 9Months, 12Months after surgery-quality of life (EORTC) questionnaire
ICU and hospital stay after surgeryTime of hospital stay (average 7days)-ICU and overall hospital stay after surgery
Patients' adjuvant treatment3Months, 6Months, 9Months, 12Months after surgery-adjuvant treatment each patient has received
Recurrent tumor growth (RANO criteria)3Months, 6Months, 9Months, 12Months after surgery-recurrent tumor growth (RANO criteria) according to local tumor boards and independent blinded analysis
Histology1 week after surgeryHistological analysis
MGMT (O6-methylguanine-DNA-methyltransferase) analysis1 week after surgeryMGMT promoter analysis (Routine molecular diagnostics)
IDH-1 (isocitrate dehydrogenase) analysis1 week after surgeryIDH-1 mutation analysis (Routine molecular diagnostics)
Progression-free survival (PFS)Day of surgery - 6 months - 12 months6M&12M-PFS
Overall survival (OS)Day of surgery - Death of patient (Max. 10 years follow-up)OS of patients
Follow-up imaging3Months, 6Months, 9Months, 12Months after surgery-follow-up imaging 3, 6, 9, 12 months postoperative incl. independent blinded analysis

Other

MeasureTime frameDescription
Preoperative tumor localization and resectability concerning eloquent regionsBlinded analysis of preoperative imaging (not older than 3 days prior to surgery)Independent blinded analysis of the preoperative imaging data by a blinded neurosurgeon with extensive experience in the resection of gliomas. Analysis will be done before the final evaluation of results. (Within 12 months)

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026