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

Primary Purpose

Glioblastoma

Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
iMRI-guided surgery
5-ALA-guided surgery
Sponsored by
University Hospital Tuebingen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Glioblastoma focused on measuring 5-ALA, Intraoperative MRI, Extent of resection

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Department of Neurosurgery, Universitätsklinikum Bonn, Bonn, Germany
  • Department of Neurosurgery, Universität zu Köln, Köln, Germany
  • Städtisches Klinikum Dresden Friedrichstadt
  • Department of Neurosurgery, Heinrich-Heine-Universität Düsseldorf, Düsseldorf
  • Department of Neurosurgery, Friedrich-Alexander-University Erlangen-Nürnberg
  • Department of Neurosurgery, Johann Wolfgang Goethe-University Frankfurt am Main
  • Department of Neurosurgery, Georg-August-Universität Göttingen, Göttingen,
  • Department of Neurosurgery, University of Ulm, Hospital Günzburg,
  • Asklepios Klinik Hamburg, Klinik für Neurochirurgie
  • International Neuroscience Institute Hannover, Hannover, Germany
  • Department of Neurosurgery, Ruprecht-Karls-University Heidelberg
  • Department of Neurosurgery, University of Schleswig-Holstein, Kiel, Germany
  • Department of Neurosurgery, Westfälische Wilhelms-Universität Münster, Münster, Germany
  • Department of Neurosurgery, Eberhard Karls University, Tübingen,
  • Department of Neurosurgery, Julius-Maximilians-Universität Würzburg

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

iMRI-guided surgery

5-ALA-guided surgery

Arm Description

Resection of Glioblastomas with iMRI-guidance

Resection of Glioblastomas with 5-ALA-fluorescence-guidance

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

Patients' clinical condition (KPS)
-KPS clinical scoring
Patients' clinical condition (NIHSS)
-NIHSS stroke score
Patients' clinical condition (QoL)
-quality of life (EORTC) questionnaire
ICU and hospital stay after surgery
-ICU and overall hospital stay after surgery
Patients' adjuvant treatment
-adjuvant treatment each patient has received
Recurrent tumor growth (RANO criteria)
-recurrent tumor growth (RANO criteria) according to local tumor boards and independent blinded analysis
Follow-up imaging
-follow-up imaging 3, 6, 9, 12 months postoperative incl. independent blinded analysis
Histology
Histological analysis
MGMT (O6-methylguanine-DNA-methyltransferase) analysis
MGMT promoter analysis (Routine molecular diagnostics)
IDH-1 (isocitrate dehydrogenase) analysis
IDH-1 mutation analysis (Routine molecular diagnostics)
Progression-free survival (PFS)
6M&12M-PFS
Overall survival (OS)
OS of patients

Full Information

First Posted
February 18, 2015
Last Updated
October 21, 2021
Sponsor
University Hospital Tuebingen
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1. Study Identification

Unique Protocol Identification Number
NCT02379572
Brief Title
Impact of iMRI on the Extent of Resection in Patients With Newly Diagnosed Glioblastomas
Official Title
Impact of iMRI on the Extent of Resection in Patients With Newly Diagnosed Glioblastomas - A Prospective Multicenter Parallel Group Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2020
Overall Recruitment Status
Completed
Study Start Date
June 2015 (undefined)
Primary Completion Date
June 2020 (Actual)
Study Completion Date
July 1, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital Tuebingen

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Glioblastoma
Keywords
5-ALA, Intraoperative MRI, Extent of resection

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Non-Randomized
Enrollment
315 (Actual)

8. Arms, Groups, and Interventions

Arm Title
iMRI-guided surgery
Arm Type
Experimental
Arm Description
Resection of Glioblastomas with iMRI-guidance
Arm Title
5-ALA-guided surgery
Arm Type
Active Comparator
Arm Description
Resection of Glioblastomas with 5-ALA-fluorescence-guidance
Intervention Type
Device
Intervention Name(s)
iMRI-guided surgery
Intervention Description
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.
Intervention Type
Drug
Intervention Name(s)
5-ALA-guided surgery
Intervention Description
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.
Primary Outcome Measure Information:
Title
Complete resections in the postoperative MRI (T1+/-CM) within 48 hours after surgery
Description
Completeness of resection in the postoperative MRI within 48h after surgery. Blinded analysis by an independent radiologist.
Time Frame
48 hour
Secondary Outcome Measure Information:
Title
Patients' clinical condition (KPS)
Description
-KPS clinical scoring
Time Frame
preoperative (day before surgery), 1 week, 3Months, 6Months, 9Months, 12Months after surgery
Title
Patients' clinical condition (NIHSS)
Description
-NIHSS stroke score
Time Frame
preoperative (day before surgery), 1 week, 3Months, 6Months, 9Months, 12Months after surgery
Title
Patients' clinical condition (QoL)
Description
-quality of life (EORTC) questionnaire
Time Frame
preoperative (day before surgery), 1 week, 3Months, 6Months, 9Months, 12Months after surgery
Title
ICU and hospital stay after surgery
Description
-ICU and overall hospital stay after surgery
Time Frame
Time of hospital stay (average 7days)
Title
Patients' adjuvant treatment
Description
-adjuvant treatment each patient has received
Time Frame
3Months, 6Months, 9Months, 12Months after surgery
Title
Recurrent tumor growth (RANO criteria)
Description
-recurrent tumor growth (RANO criteria) according to local tumor boards and independent blinded analysis
Time Frame
3Months, 6Months, 9Months, 12Months after surgery
Title
Follow-up imaging
Description
-follow-up imaging 3, 6, 9, 12 months postoperative incl. independent blinded analysis
Time Frame
3Months, 6Months, 9Months, 12Months after surgery
Title
Histology
Description
Histological analysis
Time Frame
1 week after surgery
Title
MGMT (O6-methylguanine-DNA-methyltransferase) analysis
Description
MGMT promoter analysis (Routine molecular diagnostics)
Time Frame
1 week after surgery
Title
IDH-1 (isocitrate dehydrogenase) analysis
Description
IDH-1 mutation analysis (Routine molecular diagnostics)
Time Frame
1 week after surgery
Title
Progression-free survival (PFS)
Description
6M&12M-PFS
Time Frame
Day of surgery - 6 months - 12 months
Title
Overall survival (OS)
Description
OS of patients
Time Frame
Day of surgery - Death of patient (Max. 10 years follow-up)
Other Pre-specified Outcome Measures:
Title
Preoperative tumor localization and resectability concerning eloquent regions
Description
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)
Time Frame
Blinded analysis of preoperative imaging (not older than 3 days prior to surgery)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: In MRI suspected primary singular untreated GBM Planned total resection of the tumor according to the surgeon Patient ≥18 years, ≤80 years Preoperative KPS ≥ 60%, American Society of Anesthesiologists (ASA) score 1 and 2 Patients' informed consent Exclusion Criteria: Tumors of the midline, basal ganglia, cerebellum, brain stem, eloquent areas Multifocal glioblastoma Substantial (>50%), non-contrast enhancing tumor areas suggesting low-grade glioma with malignant transformation Contraindications to MRI Inability to give consent because of language barrier or dysphasia Histological diagnosis other than Glioblastoma multiforme WHO °IV Increased risk of thrombosis (e.g. Factor V Leiden) Pregnancy or breast feeding Hypersensibility for 5-ALA oder porphyrins Acute or chronic Porphyria Renal insufficiency Hepatic insufficiency High likelihood of inability to receive adjuvant therapy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Constantin Roder, Dr.
Organizational Affiliation
University Hospital Tuebingen, Department of Neurosurgery
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Neurosurgery, Universitätsklinikum Bonn, Bonn, Germany
City
Bonn
Country
Germany
Facility Name
Department of Neurosurgery, Universität zu Köln, Köln, Germany
City
Cologne
Country
Germany
Facility Name
Städtisches Klinikum Dresden Friedrichstadt
City
Dresden
Country
Germany
Facility Name
Department of Neurosurgery, Heinrich-Heine-Universität Düsseldorf, Düsseldorf
City
Düsseldorf
Country
Germany
Facility Name
Department of Neurosurgery, Friedrich-Alexander-University Erlangen-Nürnberg
City
Erlangen
Country
Germany
Facility Name
Department of Neurosurgery, Johann Wolfgang Goethe-University Frankfurt am Main
City
Frankfurt a.M.
Country
Germany
Facility Name
Department of Neurosurgery, Georg-August-Universität Göttingen, Göttingen,
City
Göttingen
Country
Germany
Facility Name
Department of Neurosurgery, University of Ulm, Hospital Günzburg,
City
Günzburg
Country
Germany
Facility Name
Asklepios Klinik Hamburg, Klinik für Neurochirurgie
City
Hamburg
Country
Germany
Facility Name
International Neuroscience Institute Hannover, Hannover, Germany
City
Hannover
Country
Germany
Facility Name
Department of Neurosurgery, Ruprecht-Karls-University Heidelberg
City
Heidelberg
Country
Germany
Facility Name
Department of Neurosurgery, University of Schleswig-Holstein, Kiel, Germany
City
Kiel
Country
Germany
Facility Name
Department of Neurosurgery, Westfälische Wilhelms-Universität Münster, Münster, Germany
City
Münster
Country
Germany
Facility Name
Department of Neurosurgery, Eberhard Karls University, Tübingen,
City
Tübingen
Country
Germany
Facility Name
Department of Neurosurgery, Julius-Maximilians-Universität Würzburg
City
Würzburg
Country
Germany

12. IPD Sharing Statement

Learn more about this trial

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

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