Brain TumorFASTMRSINCT04233788
Metabolic Characterization of Space Occupying Lesions of the Brain
An observational study of Brain Tumor and Glioma, run by Insel Gruppe AG, University Hospital Bern at 1 site in Switzerland.
Trial summary
High field MR-technologies are expected to boost metabolic spectroscopic imaging (MRSI), but also CEST-MRI. This is due to the fact that increased SNR is available which can be used to increase the spatial resolution of all sequences, or reduction of measurement times. Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Brain Tumor, Glioma, IDH Mutation
- What is being tested?
- MR-scans using a 3T Prisma and a 7T Terra scanner (Siemens, Erlangen Germany)
- Type of treatment
- Medical device
- How many people
- 55 participants
- Where
- 1 siteSwitzerland
- Study dates
- 1 Sep 2021to 31 Dec 2025
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Study population: Healthy controls: Each of the participating healthy adult persons in the study will receive 2 out of 5 different pulse sequences which will be tested against each other (5 groups with 10 healthy controls). In each group two pulse sequences will be tested against each other at 3T and 7T. The data of the healthy controls will be used an normal values to compare patient data against. Patients: 75 patients will be also be split in 5 groups groups of 15 patients. Each patient will receive 2 out of 5 MRSI and/or CEST pulse sequences which will be tested against each other in that group. The best pulse sequence is propagated to the next group. The pulse sequences will be applied at 3T and at 7T (when available). With this approach the researchers hope to find out the most accurate sequence that predicts the IDH-status pre-operatively.
Who may be able to join
- Healthy people who are able to lie in the MR scanner for one hour;
- Patients with suspected mass in the brain
- Written informed consent
Who cannot join
- Persons under the age of 18
- Persons who are mentally unable to choose to participate
- Pregnant women
- Patients with oncological findings or neurodegenerative findings in the past
- Wearing active implants (e.g. pacemakers and neurostimulators)
- Emergency patients
- Persons with tattoos on the head or neck area
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Switzerland1 site, 1 recruiting
- Recruiting
Institute for Diagnostic and Interventional Neuroradiology, University Hospital Bern
Bern, 3010
Johannes Slotboom, PhD, +41316327469, johannes.slotboom@insel.ch
About this study
Official title: Metabolic Characterization of Space Occupying Lesions of the Brain Using in Vivo MR- (Spectroscopic) Imaging at 3 Tesla and 7 Tesla
High field MR-technologies are expected to boost metabolic spectroscopic imaging (MRSI), but also CEST-MRI. This is due to the fact that increased SNR is available which can be used to increase the spatial resolution of all sequences, or reduction of measurement times. Recent findings has shown that MRSI can be used to evaluate the isocitrate dehydrogenase (IDH) status of gliomas, a brain tumor type which is most often diagnosed in humans. Patients with IDH-mutated gliomas have a much longer survival time that IDH-wildtype. In IDH-mutated gliomas the substance 2-hydroxy-glutarate (2HG) is found, whereas in IDH-wildtype gliomas it is not.
The underlying trial aims to measure 2HG directly with different MRSI sequences at 3 Tesla (3T) and 7 Tesla (7T) magnetic field strength. Apart from MRSI-techniques for IDH-typing it has been shown that CEST-imaging can also be performed to determine the IDH-status of gliomas.
A total of 75 patients and 50 healthy controls will be examined in this study to evaluate the most accurate method for pre-operative IDH-status determination.
Read the detailed description
Introduction - Recently the first commercially available 7T MR-scanner which is approved for clinical use came on to the market. The main motivation to go to higher field strengths is the fact that better SNR can be achieved in shorter acquisition time, or higher spatial resolution can be obtained in the same measurement time. High field MRI also has drawbacks, e.g. substantially higher specific absorption rate (SAR), higher susceptibility related image distortion problems, and longer longitudinal relaxation times. Nevertheless, moving to higher fields is especially beneficial for MR-spectroscopy. This is due to the fact that better signal to noise ration (SNR) is combined with higher spectral resolution. The two most commonly used techniques for spectroscopic imaging (MRSI) are: (i.) relative slow 2D/3D techniques like PRESS and semiLASER based techniques, and (ii.) fast 3D echo planar based (EPI) techniques. Although echo planar spectroscopic imaging (EPSI) is a technique that has been introduced by Sir Peter Mansfield in the first half of 80es, the method is still continuously being improved, and recently very promising applications related to brain tumor diagnostics were published. To be mentioned in this context is the fact that the method can be combined with spectral editing for the detection of 2-hydroxy-glutarate (2HG) in glioma patients. 2HG is only present if the glioma that has mutations in the IDH-gene. It is shown that gliomas having the IDH-mutation have a much better overall survival prognosis. Apart from brain tumor typing, high resolution EPSI imaging also enables investigation the investigation of tumor infiltration using metabolic criteria. In surgery the patients' preoperative intake of the 5-aminolevulinic acid (5-ALA) before surgery selectively makes malignant glioma tissues fluorescent under blue light irradiation and tumor itself becomes clearly visible during the neurosurgical intervention. The fact that 5-ALA-guided completely-resected glioma patients have a significant longer survival time, underlines the necessity to know the exact tumor boundaries.
Aims - The major aims of the study proposed are manifold:
(i.) The development of a novel EPSI-pulse sequence utilizing 3D-radial k-space sampling schemes, that focuses on robustness w.r.t. patient motion, is robust with respect to chemical shift displacement artifacts, includes the possibility of 2HG-spectral editing, uses SAR-reduced radiofrequency (RF) pulses, and operate with total acquisition times that are acceptable for clinical routine use; (ii.) Comparison of the novel sequence with available conventional EPSI-techniques and semiLASER-based techniques for clinical routine use comparing its performance at 3T and 7T; (iii.) The development of a graphic processor unit (GPU) based fitting algorithm for quantification of 3D-radial EPSI-data based on the existing tdfdfit-algorithm; (iv.) Extension of a locally developed machine learning based automatic quality-filtering algorithm to be applied on the researchers' novel EPSI-data; (v.) Quantitative investigation on the effect spatial non-uniform transmit and receive properties for all relevant metabolites and spatial dependent signal amplitude correction schemes (extension of a locally developed method); (vi.) Investigation of the exact effects of selective excitation on J-coupled spin systems, and comparison of these effects between 3T and 7T; (vii.) Reproducibility study on 20 healthy volunteers measured twice with the same protocol (10 recorded twice at 7T and 10 recorded twice at 3T); (viii.) Pre-operative application of the best suited EPSI-pulse sequence in a total of 75 patients. All patients will be recorded at 3T as well as at 7T using the equivalent protocols; (ix.) Co-registration of pre-operative, spatially resolved 3D-EPSI-MRSI data with post-operative 3D-FLAIR and T1c-imaging in IDH-wildtype patients with had complete resection during 5-ALA guided neurosurgical interventions will provide information on whether MRSI-techniques are helpful to predict the tumor affected volume; (x.) Documentation of the location of a biopsy, histology to enable a better correlation between MR-spectroscopic patterns and histology.
(xi) Comparison of the performance of CEST versus the CMRR-semiLASER MRSI sequence w.r.t. to the prediction accuracy of the IDH-type of the glioma by the two technologies.
Methodology - The implementation of a robust EPSI sequence that uses 3D-radial k-space sampling schemes and reconstruction will be performed on Siemens IDEA developer platforms for VE- and XA-software versions. The sequence will be compared to the performance obtained with another EPSI implementation, available via Siemens, as well as the CMRR-implementation of the MEGA (MEscher-GArwood) semi-LASER (Localization by Adiabatic SElective Refocusing) for 2HG-editing (CMRR Spectroscopy Package, 2012). The quantification of the EPSI-data of the reference sequence will be performed with the MIDAS package. The EPSI-data of the novel sequence as well as MEGA-semi-LASER sequence will be quantified using a parallelized GPU-re-implementation of the tdfdfit-algorithm made available as separate plugin within jMRUI-spectroscopy package (jMRUI: java magnetic resonance user interface). Co-registration of pre-surgery EPSI-data with post-operative structural MRI-data will be performed with the SPM (Statistical Parameter Mapping) program. Further statistical analysis and machine learning algorithms will be based on statistical programming language "R". The CEST pulse sequences will be obtained via Siemens-Healthineers.
Potential significance - (a.) Pre-surgical knowledge of the IDH-status will enable better individual neurosurgical treatment of the patient; (b.) Coregistration of metabolic EPSI-data, with post-operative structural MR-data will give information on the fundamental usefulness of MRSI-techniques to detect glioma infiltration zones; (c.) Improved follow-up of IDH-mutated glioma patients, who typically have a long period of minimal progression, followed rapidly by aggressive growth and transformation to higher grade; (d.) The availability of an imaging biomarker to monitor tumor recurrence would be a major advance for all glioma patients.
- Conditions
- Brain Tumor, Glioma, IDH Mutation
- Being tested
- MR-scans using a 3T Prisma and a 7T Terra scanner (Siemens, Erlangen Germany)
- Keywords
- Magnetic Resonance Spectroscopic Imaging (MRSI), Chemical exchange saturation transfer imaging (CEST), Pulse sequence development, Preoperative prediction of IDH-status, Quantitative MR(S)I, Signal processing
- Medical subject headings
- Brain Neoplasms, Glioma
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
MR-scans using a 3T Prisma and a 7T Terra scanner (Siemens, Erlangen Germany)Device
Also called Examined are fast MRSI sequences and CEST sequences.
The MR-scans performed at 3T and 7T are performed to evaluate whether high field MR-examinations bring an advantage to the patient in determining the IDH-status of the glioma. Two MRSI/CEST sequences will be tested against each other.
| Study group | Role | What they receive |
|---|---|---|
| Sequence optimization (Healthy Control Group 1 (10 Persons)) | The MEGA-based editing sequences as well as the SLOW-EPSI sequence will be applied to this group using a 3T Prisma and a 7T Terra scanner. Data will be used for optimization of the pulse sequences.
Aim: find those sequence parameters to obtain best spectral quality data (SNR, spatial resolution versus measurement time). Receives: Device: MR-scans using a 3T Prisma and a 7T Terra scanner (Siemens, Erlangen Germany) | |
| Healthy Control Group 2 (15 Persons) | The best performing sequence which will be applied to this group using a 7T Terra scanner. Data will be used normative data for glutamate/glutamine and GABA levels in healthy controls.
Aim: normal reference data for future studies. Receives: Device: MR-scans using a 3T Prisma and a 7T Terra scanner (Siemens, Erlangen Germany) | |
| Patient Group 1: Comparison of 5 different spectral editing sequences (30 Patients) | Two editing pulse sequence types will be applied to this group at a 3T Prisma and a 7T Terra scanner. The sequences being compared are MEGA-semiLASER-SVS, MEGA-semiLASER based MRSI (on both 3T and 7T) and SLOW-EPSI (on 7T only). Receives: Device: MR-scans using a 3T Prisma and a 7T Terra scanner (Siemens, Erlangen Germany) | |
| Patient Group 1: Comparison of 4 different CEST sequences (30 Patients) | Two different CEST sequence types will be applied to this group at a 3T Prisma and a 7T Terra scanner. The CEST performance will be compared between 3T and 7T, as well which of the two types in the best on each scanner.
Aim: which of the four sequence predicts the IDH-mutation status best. Receives: Device: MR-scans using a 3T Prisma and a 7T Terra scanner (Siemens, Erlangen Germany) |
What is being measured
The primary outcome is the main question the study is designed to answer.
Optimal MR-sequence for IDH-typing
Finding the most optimal (2HG-edited, radial kspace-sampled) EPSI MRSI/CEST technique for the initial diagnosis of gliomas with respect to IDH-typing. Pre-operative knowledge of the IDH-type is important information for further neurosurgical treatment.
Measured: 48 months
Secondary outcomes (1)
Spectral/CEST pattern
The retrospective analysis of tumor affected tissue volumes identified by 3D-MRSI/CEST image data with the factual resected volumes during 5-ALA guided complete tumor resection interventions enable to find the relationship between the spectral or CEST pattern and the location of the glioma.
Measured: 48 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 Jan 2020
- Study start1 Sep 2021
- Primary completion31 Dec 2024 (estimated)
- Study completion31 Dec 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (5)Papers the sponsor has linked to this study.
- Other trials for Brain TumorStudies of the same condition, open and under way.
- More trials run by Insel Gruppe AG, University Hospital BernThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Other
- Time perspective
- Prospective
- Enrolment
- 55 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Insel Gruppe AG, University Hospital Bern
- Sponsor type
- University, hospital or other
- Collaborators
- Swiss National Science Foundation
- Responsible party
- Sponsor
- Investigators
- Johannes Slotboom, PhD, Study chair, University of Bern
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04233788
- Sponsor's protocol ID
- 2019-00503
- Other IDs
- 2019
- Acronym
- FASTMRSI
- Status last verified
- Nov 2024
- First submitted
- 15 Jan 2020
- Last updated
- 25 Nov 2024
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Paech D, Windschuh J, Oberhollenzer J, Dreher C, Sahm F, Meissner JE, Goerke S, Schuenke P, Zaiss M, Regnery S, Bickelhaupt S, Baumer P, Bendszus M, Wick W, Unterberg A, Bachert P, Ladd ME, Schlemmer HP, Radbruch A. Assessing the predictability of IDH mutation and MGMT methylation status in glioma patients using relaxation-compensated multipool CEST MRI at 7.0 T. Neuro Oncol. 2018 Nov 12;20(12):1661-1671. doi: 10.1093/neuonc/noy073.
PubMed 29733378Choi C, Ganji SK, DeBerardinis RJ, Hatanpaa KJ, Rakheja D, Kovacs Z, Yang XL, Mashimo T, Raisanen JM, Marin-Valencia I, Pascual JM, Madden CJ, Mickey BE, Malloy CR, Bachoo RM, Maher EA. 2-hydroxyglutarate detection by magnetic resonance spectroscopy in IDH-mutated patients with gliomas. Nat Med. 2012 Jan 26;18(4):624-9. doi: 10.1038/nm.2682.
PubMed 22281806Marjanska M, Auerbach EJ, Valabregue R, Van de Moortele PF, Adriany G, Garwood M. Localized 1H NMR spectroscopy in different regions of human brain in vivo at 7 T: T2 relaxation times and concentrations of cerebral metabolites. NMR Biomed. 2012 Feb;25(2):332-9. doi: 10.1002/nbm.1754. Epub 2011 Jul 27.
PubMed 21796710Sabati M, Sheriff S, Gu M, Wei J, Zhu H, Barker PB, Spielman DM, Alger JR, Maudsley AA. Multivendor implementation and comparison of volumetric whole-brain echo-planar MR spectroscopic imaging. Magn Reson Med. 2015 Nov;74(5):1209-20. doi: 10.1002/mrm.25510. Epub 2014 Oct 29.
PubMed 25354190Slotboom J, Boesch C, Kreis R. Versatile frequency domain fitting using time domain models and prior knowledge. Magn Reson Med. 1998 Jun;39(6):899-911. doi: 10.1002/mrm.1910390607.
PubMed 9621913
Study at a glance
From the registry record, last updated by the sponsor on 25 Nov 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Metabolic Characterization of Space Occupying Lesions of the Brain Using in Vivo MR- (Spectroscopic) Imaging at 3 Tesla and 7 Tesla
- ClinicalTrials.gov ID
- NCT04233788
- Acronym / sponsor ID
- FASTMRSI / 2019-00503
- Conditions
- Brain Tumor, Glioma, IDH Mutation
- Keywords
- Magnetic Resonance Spectroscopic Imaging (MRSI), Chemical exchange saturation transfer imaging (CEST), Pulse sequence development, Preoperative prediction of IDH-status, Quantitative MR(S)I, Signal processing
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 55 participants (estimated)
- Lead sponsor
- Insel Gruppe AG, University Hospital BernUniversity, hospital or other
- Collaborators
- Swiss National Science Foundation
- Study start
- 1 Sep 2021 (actual)
- Primary completion
- 31 Dec 2024 (estimated)
- Study completion
- 31 Dec 2025 (estimated)
- First posted
- 18 Jan 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
High field MR-technologies are expected to boost metabolic spectroscopic imaging (MRSI), but also CEST-MRI. This is due to the fact that increased SNR is available which can be used to increase the spatial resolution of all sequences, or reduction of measurement times. Recent findings has shown that MRSI can be used to evaluate the isocitrate dehydrogenase (IDH) status of gliomas, a brain tumor type which is most often diagnosed in humans. Patients with IDH-mutated gliomas have a much longer survival time that IDH-wildtype. In IDH-mutated gliomas the substance 2-hydroxy-glutarate (2HG) is found, whereas in IDH-wildtype gliomas it is not.
The underlying trial aims to measure 2HG directly with different MRSI sequences at 3 Tesla (3T) and 7 Tesla (7T) magnetic field strength. Apart from MRSI-techniques for IDH-typing it has been shown that CEST-imaging can also be performed to determine the IDH-status of gliomas.
A total of 75 patients and 50 healthy controls will be examined in this study to evaluate the most accurate method for pre-operative IDH-status determination.
Detailed description
Introduction - Recently the first commercially available 7T MR-scanner which is approved for clinical use came on to the market. The main motivation to go to higher field strengths is the fact that better SNR can be achieved in shorter acquisition time, or higher spatial resolution can be obtained in the same measurement time. High field MRI also has drawbacks, e.g. substantially higher specific absorption rate (SAR), higher susceptibility related image distortion problems, and longer longitudinal relaxation times. Nevertheless, moving to higher fields is especially beneficial for MR-spectroscopy. This is due to the fact that better signal to noise ration (SNR) is combined with higher spectral resolution. The two most commonly used techniques for spectroscopic imaging (MRSI) are: (i.) relative slow 2D/3D techniques like PRESS and semiLASER based techniques, and (ii.) fast 3D echo planar based (EPI) techniques. Although echo planar spectroscopic imaging (EPSI) is a technique that has been introduced by Sir Peter Mansfield in the first half of 80es, the method is still continuously being improved, and recently very promising applications related to brain tumor diagnostics were published. To be mentioned in this context is the fact that the method can be combined with spectral editing for the detection of 2-hydroxy-glutarate (2HG) in glioma patients. 2HG is only present if the glioma that has mutations in the IDH-gene. It is shown that gliomas having the IDH-mutation have a much better overall survival prognosis. Apart from brain tumor typing, high resolution EPSI imaging also enables investigation the investigation of tumor infiltration using metabolic criteria. In surgery the patients' preoperative intake of the 5-aminolevulinic acid (5-ALA) before surgery selectively makes malignant glioma tissues fluorescent under blue light irradiation and tumor itself becomes clearly visible during the neurosurgical intervention. The fact that 5-ALA-guided completely-resected glioma patients have a significant longer survival time, underlines the necessity to know the exact tumor boundaries.
Aims - The major aims of the study proposed are manifold:
(i.) The development of a novel EPSI-pulse sequence utilizing 3D-radial k-space sampling schemes, that focuses on robustness w.r.t. patient motion, is robust with respect to chemical shift displacement artifacts, includes the possibility of 2HG-spectral editing, uses SAR-reduced radiofrequency (RF) pulses, and operate with total acquisition times that are acceptable for clinical routine use; (ii.) Comparison of the novel sequence with available conventional EPSI-techniques and semiLASER-based techniques for clinical routine use comparing its performance at 3T and 7T; (iii.) The development of a graphic processor unit (GPU) based fitting algorithm for quantification of 3D-radial EPSI-data based on the existing tdfdfit-algorithm; (iv.) Extension of a locally developed machine learning based automatic quality-filtering algorithm to be applied on the researchers' novel EPSI-data; (v.) Quantitative investigation on the effect spatial non-uniform transmit and receive properties for all relevant metabolites and spatial dependent signal amplitude correction schemes (extension of a locally developed method); (vi.) Investigation of the exact effects of selective excitation on J-coupled spin systems, and comparison of these effects between 3T and 7T; (vii.) Reproducibility study on 20 healthy volunteers measured twice with the same protocol (10 recorded twice at 7T and 10 recorded twice at 3T); (viii.) Pre-operative application of the best suited EPSI-pulse sequence in a total of 75 patients. All patients will be recorded at 3T as well as at 7T using the equivalent protocols; (ix.) Co-registration of pre-operative, spatially resolved 3D-EPSI-MRSI data with post-operative 3D-FLAIR and T1c-imaging in IDH-wildtype patients with had complete resection during 5-ALA guided neurosurgical interventions will provide information on whether MRSI-techniques are helpful to predict the tumor affected volume; (x.) Documentation of the location of a biopsy, histology to enable a better correlation between MR-spectroscopic patterns and histology.
(xi) Comparison of the performance of CEST versus the CMRR-semiLASER MRSI sequence w.r.t. to the prediction accuracy of the IDH-type of the glioma by the two technologies.
Methodology - The implementation of a robust EPSI sequence that uses 3D-radial k-space sampling schemes and reconstruction will be performed on Siemens IDEA developer platforms for VE- and XA-software versions. The sequence will be compared to the performance obtained with another EPSI implementation, available via Siemens, as well as the CMRR-implementation of the MEGA (MEscher-GArwood) semi-LASER (Localization by Adiabatic SElective Refocusing) for 2HG-editing (CMRR Spectroscopy Package, 2012). The quantification of the EPSI-data of the reference sequence will be performed with the MIDAS package. The EPSI-data of the novel sequence as well as MEGA-semi-LASER sequence will be quantified using a parallelized GPU-re-implementation of the tdfdfit-algorithm made available as separate plugin within jMRUI-spectroscopy package (jMRUI: java magnetic resonance user interface). Co-registration of pre-surgery EPSI-data with post-operative structural MRI-data will be performed with the SPM (Statistical Parameter Mapping) program. Further statistical analysis and machine learning algorithms will be based on statistical programming language "R". The CEST pulse sequences will be obtained via Siemens-Healthineers.
Potential significance - (a.) Pre-surgical knowledge of the IDH-status will enable better individual neurosurgical treatment of the patient; (b.) Coregistration of metabolic EPSI-data, with post-operative structural MR-data will give information on the fundamental usefulness of MRSI-techniques to detect glioma infiltration zones; (c.) Improved follow-up of IDH-mutated glioma patients, who typically have a long period of minimal progression, followed rapidly by aggressive growth and transformation to higher grade; (d.) The availability of an imaging biomarker to monitor tumor recurrence would be a major advance for all glioma patients.
Study design
- Observational model
- Other
- Time perspective
- Prospective
- Number of arms
- 4
| Arm | Type | Receives |
|---|---|---|
| Sequence optimization (Healthy Control Group 1 (10 Persons)) | – | Device: MR-scans using a 3T Prisma and a 7T Terra scanner (Siemens, Erlangen Germany)The MEGA-based editing sequences as well as the SLOW-EPSI sequence will be applied to this group using a 3T Prisma and a 7T Terra scanner. Data will be used for optimization of the pulse sequences. Aim: find those sequence parameters to obtain best spectral quality data (SNR, spatial resolution versus measurement time). |
| Healthy Control Group 2 (15 Persons) | – | Device: MR-scans using a 3T Prisma and a 7T Terra scanner (Siemens, Erlangen Germany)The best performing sequence which will be applied to this group using a 7T Terra scanner. Data will be used normative data for glutamate/glutamine and GABA levels in healthy controls. Aim: normal reference data for future studies. |
| Patient Group 1: Comparison of 5 different spectral editing sequences (30 Patients) | – | Device: MR-scans using a 3T Prisma and a 7T Terra scanner (Siemens, Erlangen Germany)Two editing pulse sequence types will be applied to this group at a 3T Prisma and a 7T Terra scanner. The sequences being compared are MEGA-semiLASER-SVS, MEGA-semiLASER based MRSI (on both 3T and 7T) and SLOW-EPSI (on 7T only). |
| Patient Group 1: Comparison of 4 different CEST sequences (30 Patients) | – | Device: MR-scans using a 3T Prisma and a 7T Terra scanner (Siemens, Erlangen Germany)Two different CEST sequence types will be applied to this group at a 3T Prisma and a 7T Terra scanner. The CEST performance will be compared between 3T and 7T, as well which of the two types in the best on each scanner. Aim: which of the four sequence predicts the IDH-mutation status best. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- Healthy controls: Each of the participating healthy adult persons in the study will receive 2 out of 5 different pulse sequences which will be tested against each other (5 groups with 10 healthy controls). In each group two pulse sequences will be tested against each other at 3T and 7T. The data of the healthy controls will be used an normal values to compare patient data against. Patients: 75 patients will be also be split in 5 groups groups of 15 patients. Each patient will receive 2 out of 5 MRSI and/or CEST pulse sequences which will be tested against each other in that group. The best pulse sequence is propagated to the next group. The pulse sequences will be applied at 3T and at 7T (when available). With this approach the researchers hope to find out the most accurate sequence that predicts the IDH-status pre-operatively.
Key inclusion criteria (3 listed)
- Healthy people who are able to lie in the MR scanner for one hour;
- Patients with suspected mass in the brain
- Written informed consent
Key exclusion criteria (7 listed)
- Persons under the age of 18
- Persons who are mentally unable to choose to participate
- Pregnant women
- Patients with oncological findings or neurodegenerative findings in the past
- Wearing active implants (e.g. pacemakers and neurostimulators)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| MR-scans using a 3T Prisma and a 7T Terra scanner (Siemens, Erlangen Germany)Also: Examined are fast MRSI sequences and CEST sequences.The MR-scans performed at 3T and 7T are performed to evaluate whether high field MR-examinations bring an advantage to the patient in determining the IDH-status of the glioma. Two MRSI/CEST sequences will be tested against each other. | Device | Healthy Control Group 2 (15 Persons), Patient Group 1: Comparison of 4 different CEST sequences (30 Patients), Patient Group 1: Comparison of 5 different spectral editing sequences (30 Patients), Sequence optimization (Healthy Control Group 1 (10 Persons)) |
Primary outcome
Optimal MR-sequence for IDH-typing
Time frame: 48 months
Finding the most optimal (2HG-edited, radial kspace-sampled) EPSI MRSI/CEST technique for the initial diagnosis of gliomas with respect to IDH-typing. Pre-operative knowledge of the IDH-type is important information for further neurosurgical treatment.
1 secondary outcome
Spectral/CEST pattern
Time frame: 48 months
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 25 Nov 2024.
- Background: PubMed 29733378Paech D, Windschuh J, Oberhollenzer J, Dreher C, Sahm F, Meissner JE, Goerke S, Schuenke P, Zaiss M, Regnery S, Bickelhaupt S, Baumer P, Bendszus M, Wick W, Unterberg A, Bachert P, Ladd ME, Schlemmer HP, Radbruch A. Assessing the predictability of IDH mutation and MGMT methylation status in glioma patients using relaxation-compensated multipool CEST MRI at 7.0 T. Neuro Oncol. 2018 Nov 12;20(12):1661-1671. doi: 10.1093/neuonc/noy073.
- Background: PubMed 22281806Choi C, Ganji SK, DeBerardinis RJ, Hatanpaa KJ, Rakheja D, Kovacs Z, Yang XL, Mashimo T, Raisanen JM, Marin-Valencia I, Pascual JM, Madden CJ, Mickey BE, Malloy CR, Bachoo RM, Maher EA. 2-hydroxyglutarate detection by magnetic resonance spectroscopy in IDH-mutated patients with gliomas. Nat Med. 2012 Jan 26;18(4):624-9. doi: 10.1038/nm.2682.
- Background: PubMed 21796710Marjanska M, Auerbach EJ, Valabregue R, Van de Moortele PF, Adriany G, Garwood M. Localized 1H NMR spectroscopy in different regions of human brain in vivo at 7 T: T2 relaxation times and concentrations of cerebral metabolites. NMR Biomed. 2012 Feb;25(2):332-9. doi: 10.1002/nbm.1754. Epub 2011 Jul 27.
- Background: PubMed 25354190Sabati M, Sheriff S, Gu M, Wei J, Zhu H, Barker PB, Spielman DM, Alger JR, Maudsley AA. Multivendor implementation and comparison of volumetric whole-brain echo-planar MR spectroscopic imaging. Magn Reson Med. 2015 Nov;74(5):1209-20. doi: 10.1002/mrm.25510. Epub 2014 Oct 29.
- Background: PubMed 9621913Slotboom J, Boesch C, Kreis R. Versatile frequency domain fitting using time domain models and prior knowledge. Magn Reson Med. 1998 Jun;39(6):899-911. doi: 10.1002/mrm.1910390607.
- Individual participant dataSharing planned: No
Related trials for Brain Tumor
RecruitingPhase 3
Beginning Radiation Immediately With GammaTile at GBM Excision Versus Standard of Care
Glioblastoma
RecruitingPhase 2
BrAin Metastasis in tripLe Negateive Breast Cancer: IvoneScimab and Trop2 ADC
Triple-Negative Breast Cancer (TNBC), Brain Metastases
RecruitingPhase 1/2
Testing the Addition of an Anti-cancer Drug, Selinexor, to the Usual Chemotherapy Treatment (Temozolomide) for Brain Tumors That Have Returned After Previous Treatment
Recurrent Glioblastoma, IDH-Wildtype, Recurrent MGMT-Methylated Glioblastoma
Active, not recruiting
Effects of Whole-body Electrical Muscle Stimulation Exercise on Adults With Neuromuscular Disease
Neuromuscular Diseases (NMD), Amyotrophic Lateral Sclerosis
Active, not recruitingPhase 1
Prospective Exploratory Study of FAPi PET/CT With Histopathology Validation in Patients With Various Cancers
Bladder Carcinoma, Cervical Carcinoma
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Johannes Slotboom, PhD study chair
University of Bern
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Brain Tumor and Glioma, run by Insel Gruppe AG, University Hospital Bern at 1 site in Switzerland.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 25 Nov 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Switzerland. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Johannes Slotboom, PhD (+41316327469, johannes.slotboom@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Optimal MR-sequence for IDH-typing (time frame: 48 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT04233788, which also lists 5 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 25 Nov 2024.