Glioblastoma Radiotherapy Using IMRT or Proton Beams (GRIPS)
Primary Purpose
Glioblastoma
Status
Recruiting
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Proton irradiation
Photon irradiation
Sponsored by
About this trial
This is an interventional treatment trial for Glioblastoma
Eligibility Criteria
Inclusion Criteria:
- histologically confirmed gliomblastoma WHO IV (operated or after biopsy)
- Indication for radiotherapy / radiochemotherapy
- Informed consent
- KI ≥ 60% or ECOG 0/1
- Age ≥ 18 years
- Sufficient effective contraception
Exclusion Criteria:
- Patient is not able to consent
- Previous radiotherapy in the brain or skull base
- Active medical implants for which there is no ion radiation authorization at the time of treatment (e.g., cardiac pacemaker, defibrillator, ...)
- Contraindication to MRI imaging
- Simultaneous participation in another clinical trial that could influence the outcome of this study or other study
Sites / Locations
- Universitätsklinikum HeidelbergRecruiting
- Universitätsklinikum Gießen und Marburg
- Klinikum Stuttgart
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Arm A: Proton irradiation
Arm B: Photon IMRT
Arm Description
Irradiation applied with protons
Photon irradiation applied as intensity-modulated radiotherapy
Outcomes
Primary Outcome Measures
Cumulative rate of toxicity
Cumulative rate of toxicity ≥ grade 2 (until progress (max. month 4))
Secondary Outcome Measures
Progression free survival
Progression free survival
Overall survival
Overall survival
Acute Toxicity
according to CTC AE V5.0
Late Toxicity
according to CTC AE V5.0
Quality of life according to EORTC QLQ-C30
according to EORTC QLQ-C30
Quality of life according to EORTC QLQ-BN20
according to EORTC QLQ-BN20
Neurocognition
according to Hopkins Verbal Learning Test-Revised
Measuring number of Lymphocytes count
Full Information
NCT ID
NCT04752280
First Posted
February 9, 2021
Last Updated
April 19, 2021
Sponsor
University Hospital Heidelberg
1. Study Identification
Unique Protocol Identification Number
NCT04752280
Brief Title
Glioblastoma Radiotherapy Using IMRT or Proton Beams
Acronym
GRIPS
Official Title
Glioblastoma Radiotherapy Using IMRT or Proton Beams
Study Type
Interventional
2. Study Status
Record Verification Date
April 2021
Overall Recruitment Status
Recruiting
Study Start Date
April 19, 2021 (Actual)
Primary Completion Date
August 19, 2025 (Anticipated)
Study Completion Date
October 19, 2027 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital Heidelberg
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Radiation therapy is an integral part of the multimodal primary therapy of glioblastomas. As the overall prognosis in this tumor entity remains unfavorable, current research is focused on additional drug therapies, which are often accompanied by increases in toxicity. By using proton beams instead of photon beams, it is possible to protect large parts of the brain which are not affected by the tumor more effectively. An initial retrospective matched-pair analysis showed that this theoretical physical benefit is also clinically associated with a reduction in toxicity during therapy and in the first few months thereafter. The aim of the GRIPS study is to prospectively test this clinical benefit in a randomized, open-label Phase III study. Patients are treated in the study using either modern photon radiation techniques (standard arm) or proton beams (experimental arm). The primary endpoint is the cumulative toxicity CTC grade 2 and higher in the first 4 months. Secondary endpoints include overall survival, progression-free survival, quality of life, and neurocognition.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Glioblastoma
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
326 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Arm A: Proton irradiation
Arm Type
Experimental
Arm Description
Irradiation applied with protons
Arm Title
Arm B: Photon IMRT
Arm Type
Active Comparator
Arm Description
Photon irradiation applied as intensity-modulated radiotherapy
Intervention Type
Radiation
Intervention Name(s)
Proton irradiation
Intervention Description
proton irradiation applied as follows: 30 x 2 Gy(RBE) 33 x 1,8 Gy (RBE), or 15 x 2,67 Gy (RBE)
Intervention Type
Radiation
Intervention Name(s)
Photon irradiation
Intervention Description
proton irradiation applied as follows: 30 x 2 Gy 33 x 1,8 Gy, or 15 x 2,67 Gy
Primary Outcome Measure Information:
Title
Cumulative rate of toxicity
Description
Cumulative rate of toxicity ≥ grade 2 (until progress (max. month 4))
Time Frame
from start of radiotherapy until progress (max. month 4)
Secondary Outcome Measure Information:
Title
Progression free survival
Description
Progression free survival
Time Frame
1 year and 2 years
Title
Overall survival
Description
Overall survival
Time Frame
1 year and 2 years
Title
Acute Toxicity
Description
according to CTC AE V5.0
Time Frame
start of therapy until 6 weeks after end of therapy (end of therapy up to month 4)
Title
Late Toxicity
Description
according to CTC AE V5.0
Time Frame
6 weeks after end of therapy (end of therapy up to month 4)
Title
Quality of life according to EORTC QLQ-C30
Description
according to EORTC QLQ-C30
Time Frame
1 year and 2 years
Title
Quality of life according to EORTC QLQ-BN20
Description
according to EORTC QLQ-BN20
Time Frame
1 year and 2 years
Title
Neurocognition
Description
according to Hopkins Verbal Learning Test-Revised
Time Frame
1 year and 2 years
Title
Measuring number of Lymphocytes count
Time Frame
end of therapy up to month 4
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
histologically confirmed gliomblastoma WHO IV (operated or after biopsy)
Indication for radiotherapy / radiochemotherapy
Informed consent
KI ≥ 60% or ECOG 0/1
Age ≥ 18 years
Sufficient effective contraception
Exclusion Criteria:
Patient is not able to consent
Previous radiotherapy in the brain or skull base
Active medical implants for which there is no ion radiation authorization at the time of treatment (e.g., cardiac pacemaker, defibrillator, ...)
Contraindication to MRI imaging
Simultaneous participation in another clinical trial that could influence the outcome of this study or other study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Klaus Herfarth, Prof. Dr.
Phone
+49 6221 56 34093
Email
studienkoordination.RAD@med.uni-heidelberg.de
Facility Information:
Facility Name
Universitätsklinikum Heidelberg
City
Heidelberg
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Klaus Herfarth, Prof. Dr.
Facility Name
Universitätsklinikum Gießen und Marburg
City
Marburg
Country
Germany
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rita Engenhart-Cabillic, Prof. Dr.
Facility Name
Klinikum Stuttgart
City
Stuttgart
Country
Germany
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marc Münter, Prof. Dr.
12. IPD Sharing Statement
Citations:
PubMed Identifier
34930368
Citation
Konig L, Jakel C, von Knebel Doeberitz N, Kieser M, Eberle F, Munter M, Debus J, Herfarth K. Glioblastoma radiotherapy using Intensity modulated Radiotherapy (IMRT) or proton Radiotherapy-GRIPS Trial (Glioblastoma Radiotherapy via IMRT or Proton BeamS): a study protocol for a multicenter, prospective, open-label, randomized, two-arm, phase III study. Radiat Oncol. 2021 Dec 20;16(1):240. doi: 10.1186/s13014-021-01962-8.
Results Reference
derived
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Glioblastoma Radiotherapy Using IMRT or Proton Beams
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