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Can Hybrid PET-MRI Differentiate Between Radiation Effects and Disease Progression?

Primary Purpose

Brain Tumor

Status
Unknown status
Phase
Not Applicable
Locations
Israel
Study Type
Interventional
Intervention
PET MR
Sponsored by
Assuta Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Brain Tumor focused on measuring PET, MRI, BRAIN METASTASIS, BRAIN PRIMARY TUMOR, RESPONSE TO TREATMENT

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Subject with glial brain tumors,
  • Subjects with metastatic brain tumors that were treated with stereotactic radiation (SRS), * Subjects with metastatic brain tumors which were not treated

Exclusion Criteria:

  • glial tumor with no histological diagnosis
  • non breast of lung metastasis
  • non compliance
  • unable to lay still during the scanning
  • mri non
  • renal failure/gadolinium sensitivity
  • less than 5 mm metastatic tumors
  • bleeding brain tumors
  • pregnancy

Sites / Locations

  • Assuta Medical CentersRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Other

Other

Other

Arm Label

PRIMARY BRAIN TUMOR (PBT)

METASTATIC BT TREATED BY SRS

METASTATIC BT NOT TREATED BY SRS

Arm Description

patients with PBT (Glioblastoma, Anaplastic Astrocytoma, Anaplastic Oligodendroglioma, Anaplastic Oligoastrocytoma), before treatment with radiation and chemotherapy.will be followed with PET MRI

patients with lung or breast metastasis to brain treated by SRS in which at least one lesion showed deterioration by MR performed after treatment. will be followed with PET MRI

patients with lung or breast metastasis to brain where the SRS treatment was postponed for clinical reasons (getting mutation information for targeted treatment) the lesion size measures 5-40 mm. will be followed with PET MRI

Outcomes

Primary Outcome Measures

Distinguish between progressive tumor and treatment related effects
finding PET-MRI difference between progression and treatment effect correlating with clinical out come

Secondary Outcome Measures

Full Information

First Posted
February 20, 2017
Last Updated
March 20, 2017
Sponsor
Assuta Medical Center
Collaborators
Rabin Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT03068520
Brief Title
Can Hybrid PET-MRI Differentiate Between Radiation Effects and Disease Progression?
Official Title
Imaging After Stereotactic Radiosurgery for Brain Metastases or Primary Tumor Can Hybrid PET-MRI Differentiate Between Radiation Effects and Disease ?
Study Type
Interventional

2. Study Status

Record Verification Date
March 2017
Overall Recruitment Status
Unknown status
Study Start Date
March 1, 2017 (Actual)
Primary Completion Date
December 31, 2017 (Anticipated)
Study Completion Date
December 31, 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Assuta Medical Center
Collaborators
Rabin Medical 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
PET-MRI scanning regarding amino acid metabolic profile, functional and morphological details will be performed on set intervals to patients with brain tumor & brain metastases in order to try to optimize the study protocol, distinguish between pseudo-response to anti-angiogenic therapy and tumor progression, and most importantly try to distinguish between progressive tumor and treatment related effects.3 cohort of patients will be included in the study.
Detailed Description
The multimodality approach for management of primary and secondary brain tumors includes surgery, radiotherapy and chemotherapy. Determination of an objective response to treatment relies on imaging findings (e.g. CT, MRI, PET).During the course of the disease patients with brain tumors often develop new or worsening contrast-enhancing lesions on routine follow-up imaging.These lesions may reflect tumor recurrence, treatment effect, or a combination of both. Discerning between tumor recurrence and treatment effect is clinically significant issue and a major challenge in neuro-oncology. Treatment-related effects exist within a spectrum, with "pseudoprogression" reflecting subacute and often transient injury, and "radiation necrosis" reflecting later and more permanent damage.The difficulty in differentiating tumor progression from treatment-related effects has serious implications for individual patient treatment decisions and prognosis as well as for clinical trial design and interpretation of results. A contemporary hybrid scanner technology is capable of acquiring both metabolic information from PET and morphological and functional details from MRI. This new integrated technique opens new horizons for clinical and research evaluation of brain tumors and the associated treatment effects. The aim of the current study is to use the combined data obtained by PET-MRI scanning regarding amino acid metabolic profile, functional and morphological details in order to: Distinguish between progressive tumor and treatment related effects To identify pseudo-response to antiangiogenic therapy from tumor progression To optimize the study protocol of PET-MRI for future routine clinical application. The study will include three cohorts of patients with brain tumors: Primary brain tumors: A cohort of 60 adult patients (age: 18-70) with newly diagnosed high grade gliomas (Glioblastoma, Anaplastic Astrocytoma, Anaplastic Oligodendroglioma, Anaplastic Oligoastrocytoma) scheduled for a combined treatment with chemotherapy and radiotherapy. Patients will be eligible for the study immediately after receiving the pathological diagnosis and prior to any further treatment. These patients will undergo the PET-MRI scanning at 4 time points as follows: 1st scan: after surgery or biopsy and before any further treatment 2nd scan: will be performed up to 4 weeks after completing the combined radiotherapy and chemotherapy regimen. 3rd and 4th scans: will follow with interval of 3 months between studies. Additional scans will be performed by the decision of the investigators or when the patient is scheduled for antiangiogenic therapy Brain metastases treated with stereotactic radiosurgery (SRS): A cohort of 60 adult patients (age: 18-75) who are being followed after SRS treatment for brain metastases secondary to breast or lung cancer whose recent imaging showed signs of progression in at list one of the previously treated lesion. Progression will be determined by Response Assessment in Neuro-Oncology Criteria (RANO criteria) for brain metastases. Number of target lesions should not exceed 4 with size of lesions ranging between 5-40 mm. These patients will undergo the PET-MRI scanning at three time points as follows: 1st scan: Following determination of progression of SRS treated lesion based on standard surveillance MRI 2nd and 3rd scans: will be performed every 2 months after the first scan Additional scans will be performed by the decision of the investigators Brain metastases not treated with SRS/radiotherapy A cohort of 20 adult patients (age: 18-75) with a diagnosis of brain metastases secondary to human epidermal growth factor receptor 2 (HER2) positive breast cancer or anaplastic lymphoma kinase (ALK) or Epidermal Growth Factor Receptor (EGFR) gene mutant lung cancer who might be candidate for SRS treatment and in whom targeted therapy is selected instead. The size of the lesions should range between 5-40 mm. These patients will undergo the PET-MRI scanning at three time points as follows: 1st scan: after the first documentation of brain metastases on standard MRI 2nd and 3rd scans: will be performed every 2 months after the first scan In case of progression and SRS treatment follow-up scanning will be performed every 2 months Additional scans will be performed by the decision of the investigators

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Brain Tumor
Keywords
PET, MRI, BRAIN METASTASIS, BRAIN PRIMARY TUMOR, RESPONSE TO TREATMENT

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
to use the combined data obtained by PET-MRI scanning regarding amino acid metabolic profile, functional and morphological details in order to: Distinguish between progressive tumor and treatment related effects To identify pseudoresponse to antiangiogenic therapy from tumor progression To optimize the study protocol of PET-MRI for future routine clinical application.
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
140 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
PRIMARY BRAIN TUMOR (PBT)
Arm Type
Other
Arm Description
patients with PBT (Glioblastoma, Anaplastic Astrocytoma, Anaplastic Oligodendroglioma, Anaplastic Oligoastrocytoma), before treatment with radiation and chemotherapy.will be followed with PET MRI
Arm Title
METASTATIC BT TREATED BY SRS
Arm Type
Other
Arm Description
patients with lung or breast metastasis to brain treated by SRS in which at least one lesion showed deterioration by MR performed after treatment. will be followed with PET MRI
Arm Title
METASTATIC BT NOT TREATED BY SRS
Arm Type
Other
Arm Description
patients with lung or breast metastasis to brain where the SRS treatment was postponed for clinical reasons (getting mutation information for targeted treatment) the lesion size measures 5-40 mm. will be followed with PET MRI
Intervention Type
Diagnostic Test
Intervention Name(s)
PET MR
Intervention Description
PET MR with 18 Fluorodopa ([18F]-DOPA) will be performed on patient at set intervals
Primary Outcome Measure Information:
Title
Distinguish between progressive tumor and treatment related effects
Description
finding PET-MRI difference between progression and treatment effect correlating with clinical out come
Time Frame
1st scan: after surgery or biopsy and before any further treatment - 2nd scan: up to 4 weeks after completing the combined radiotherapy and chemotherapy regimen. - 3rd and 4th scans - 3 month interval apart

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Subject with glial brain tumors, Subjects with metastatic brain tumors that were treated with stereotactic radiation (SRS), * Subjects with metastatic brain tumors which were not treated Exclusion Criteria: glial tumor with no histological diagnosis non breast of lung metastasis non compliance unable to lay still during the scanning mri non renal failure/gadolinium sensitivity less than 5 mm metastatic tumors bleeding brain tumors pregnancy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Michal Guindy, MD
Phone
972-50-8800102
Email
micahlgu@assuta.co.il
First Name & Middle Initial & Last Name or Official Title & Degree
Judith Luckman, MD
Phone
972-54-4858197
Email
judithl@assuta.co.il
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michal Guindy, MD
Organizational Affiliation
Assuta Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Assuta Medical Centers
City
Tel Aviv
Country
Israel
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Judith LuKman, MD
Phone
972-544858197
Email
Gudithl@assuta.co.il@assuta.co.il
First Name & Middle Initial & Last Name & Degree
Michal Guindy, MD
Phone
972-50-8800102
Email
michalgu@assuta.co.il

12. IPD Sharing Statement

Plan to Share IPD
No
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Can Hybrid PET-MRI Differentiate Between Radiation Effects and Disease Progression?

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