FET-PET Directed Simultaneous In-field Boost for Primary GBM (dualFETboost)
Primary Purpose
Glioblastoma Multiforme
Status
Completed
Phase
Not Applicable
Locations
Poland
Study Type
Interventional
Intervention
Moderately Hypofractionated Radiotherapy using Simultaneous In-Field Boost
Sponsored by
About this trial
This is an interventional treatment trial for Glioblastoma Multiforme focused on measuring FET-PET, Boost, Glioblastoma, Dose-intesification, Dose-escalation
Eligibility Criteria
Inclusion Criteria:
- Histopathological confirmation of glioblastoma (WHO grade IV)
- Age between 18-75 years of age
- General condition according to the Zubrod scale 0 or 2
- The results of the blood counts are normal
- Liver enzyme parameters normal
- The results of the parameters of the patient's functions are normal
- Informed consent to participate in the category
Exclusion Criteria:
- Coexistence of another cancer
- The location of the tumor in the area of the brain stem or cerebellum
- Prior brain radiation therapy
- No uptake visible in the FET-PET imaging
- Contraindications for MRI
- Contraindications to radiotherapy or chemotherapy
- Pregnancy, lack of consent to the use of protection against pregnancy, puerperium
- Alcohol addiction
- Mental illness
- Claustrophobia
Sites / Locations
- The Franciszek Lukaszczyk Oncology Center
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Simultaneous In-Field Boost on FET-PET positive target volumes
Arm Description
Outcomes
Primary Outcome Measures
Overall survival
From date of surgery until the date of death from any cause, percent of patient that are alive 1 and 2 years after surgery
Secondary Outcome Measures
Progression Free Survival
from the date of surgery until progression of the disease or the date of death from any cause assessed
Objective response
according to Rano criteria; from the end of radiation therapy
Location of treatment failure
from the end of radiation therapy up to progression until progression of the disease or the date of death from any cause; according to irradiation field
Radiation necrosis
from the end of radiation therapy up to progression until progression of the disease or the date of death from any cause; histopathological diagnosis of radiation necrosis
Side effects
from the end of radiation therapy up to progression until progression of the disease or the date of death from any cause; CTCAE grade 3 or higher
Full Information
NCT ID
NCT04790097
First Posted
January 23, 2021
Last Updated
May 4, 2021
Sponsor
Prof. Franciszek Lukaszczyk Memorial Oncology Center
1. Study Identification
Unique Protocol Identification Number
NCT04790097
Brief Title
FET-PET Directed Simultaneous In-field Boost for Primary GBM
Acronym
dualFETboost
Official Title
Safety and Preliminary Efficacy of Hipofractionated Irradiation Based on Dual FET-PET in Patients With Primary Glioblastoma Multiforme With Concomitant Temozolomide
Study Type
Interventional
2. Study Status
Record Verification Date
May 2021
Overall Recruitment Status
Completed
Study Start Date
February 21, 2017 (Actual)
Primary Completion Date
December 30, 2019 (Actual)
Study Completion Date
December 30, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Prof. Franciszek Lukaszczyk Memorial Oncology Center
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
The combination of anatomical MRI examination with functional examination of tissue metabolic activity such as FET-PET (PET using the radiotracer - 18F-fluoro-ethyl-tyrosine) is a valuable tool to determine the actual tumor infiltration. The FET-PET examination can be performed using the dual-time point aqusition of FET for exact treatment planning. It has also been proven that using the dual FET-PET method, it is possible to obtain a precise image of the glioblastoma infiltration corresponding to the location and shape of the recurrence, and the tumor volumes in dual FET-PET are significantly larger than in MRI. Moreover, tumor defined in dual FET-PET is different than that of the tumor defined in single FET-PET acquisition.
In the DualFETboosT trial we plan to assess the safety and preliminary efficacy of hypofractionated irraditon using simultaneous in-field boost directed on dual FET-PET based tumor volumes for treatment of primary glioblastoma multiforme with concomitant temozolomide.
Detailed Description
In the case of the treatment of glioblastoma multiforme, as a standard, radiotherapy lasts 6 weeks, and the extension of treatment may adversely affect the tumor cells death, the patient's well-being and treatment costs (prolonged hospitalization). In turn, escalating the dose may increase the toxicity of radiation therapy by increasing DNA damage in healthy brain tissue. Using of dual FET-PET images for treatment planning allow to reduce volumes of healthy tissue irradiated. Dose-intensification proposed in the study using simultaneous in-field boost allows the dose escalation without increasing the overall treatment time. All patient will be treated with moderately hypofractionated radiotherapy (2.6 Gy per fraction) directed on PET positive volumes and conventional fractionation (60Gy in 30 fractions) on tumor margin.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Glioblastoma Multiforme
Keywords
FET-PET, Boost, Glioblastoma, Dose-intesification, Dose-escalation
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
17 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Simultaneous In-Field Boost on FET-PET positive target volumes
Arm Type
Experimental
Intervention Type
Radiation
Intervention Name(s)
Moderately Hypofractionated Radiotherapy using Simultaneous In-Field Boost
Intervention Description
78Gy in 30 fractions on FET-PET based target volumes;
60Gy in 30 fractions on 2cm margin from MRI based target volumes;
all patients will be treated with concomitant and adjuvant temozolomide
Primary Outcome Measure Information:
Title
Overall survival
Description
From date of surgery until the date of death from any cause, percent of patient that are alive 1 and 2 years after surgery
Time Frame
assessed up to 24 months
Secondary Outcome Measure Information:
Title
Progression Free Survival
Description
from the date of surgery until progression of the disease or the date of death from any cause assessed
Time Frame
up to 24 months
Title
Objective response
Description
according to Rano criteria; from the end of radiation therapy
Time Frame
up to 9 months
Title
Location of treatment failure
Description
from the end of radiation therapy up to progression until progression of the disease or the date of death from any cause; according to irradiation field
Time Frame
up to 24 months
Title
Radiation necrosis
Description
from the end of radiation therapy up to progression until progression of the disease or the date of death from any cause; histopathological diagnosis of radiation necrosis
Time Frame
assessed up to 24 months
Title
Side effects
Description
from the end of radiation therapy up to progression until progression of the disease or the date of death from any cause; CTCAE grade 3 or higher
Time Frame
up to 6 months
Other Pre-specified Outcome Measures:
Title
FET predictive value
Description
From date of surgery until the date of death from any cause, Correlation between FET uptake and survival
Time Frame
up to 24 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Histopathological confirmation of glioblastoma (WHO grade IV)
Age between 18-75 years of age
General condition according to the Zubrod scale 0 or 2
The results of the blood counts are normal
Liver enzyme parameters normal
The results of the parameters of the patient's functions are normal
Informed consent to participate in the category
Exclusion Criteria:
Coexistence of another cancer
The location of the tumor in the area of the brain stem or cerebellum
Prior brain radiation therapy
No uptake visible in the FET-PET imaging
Contraindications for MRI
Contraindications to radiotherapy or chemotherapy
Pregnancy, lack of consent to the use of protection against pregnancy, puerperium
Alcohol addiction
Mental illness
Claustrophobia
Facility Information:
Facility Name
The Franciszek Lukaszczyk Oncology Center
City
Bydgoszcz
Country
Poland
12. IPD Sharing Statement
Citations:
PubMed Identifier
35552391
Citation
Harat M, Blok M, Miechowicz I, Wiatrowska I, Makarewicz K, Malkowski B. Safety and Efficacy of Irradiation Boost Based on 18F-FET-PET in Patients with Newly Diagnosed Glioblastoma. Clin Cancer Res. 2022 Jul 15;28(14):3011-3020. doi: 10.1158/1078-0432.CCR-22-0171.
Results Reference
derived
Learn more about this trial
FET-PET Directed Simultaneous In-field Boost for Primary GBM
We'll reach out to this number within 24 hrs