In Vivo Succinate Detection After External Beam Radiation Therapy in SDHx- Paragangliomas (RADIOSUCCES)
Primary Purpose
Paraganglioma of Head and Neck
Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
1H-Spectroscopy MRI
Sponsored by
About this trial
This is an interventional diagnostic trial for Paraganglioma of Head and Neck focused on measuring Paraganglioma,SDHx genes, 1H-Spectroscopy MRI
Eligibility Criteria
Inclusion Criteria:
- Age ≥ 18 years
- Signed informed consent
- Patient with cervical PGL with planning of treatment with EBR
- Patient with an SDHx mutation or unknown genetic status
- Patient affiliated to a social security scheme
Exclusion Criteria:
- Pregnant woman
- Contraindication to MRI (implantable device, etc.)
- Impossibility of lying down without movement for 45 minutes (hyperalgesic patient, claustrophobia, etc.)
- PPGL having previously been the subject of local (excluding surgery) or systemic treatment
- PPGL <1 cm longest axis
- Patient under guardianship or curatorship
Sites / Locations
- Hôpital LariboisièreRecruiting
- Hôpital Pitié-SalpêtrièreRecruiting
- Hopital européen Georges PompidouRecruiting
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
Assigned Intervention
Arm Description
Addition to the cervical angio-MRI, of a sequence of 1H-SRM 3T (SUCCESS) centered on the lesion studied, performed according to the following parameters: PRESS asymmetric monovoxel "PROBE", TE 144 ms, TR 2500 ms, 768 or 1024 medium.
Outcomes
Primary Outcome Measures
Disappearance of succinate accumulation at M12
Absence of succinate accumulation detected in vivo by 1H-SRM, in cervical PGLs with SDHx mutations, at 12 months after EBR, reviewed by 2 independant experts blinded to all other clinical and genetics data.
Secondary Outcome Measures
Disapperance of succinate accumulation at M3
Absence of succinate accumulation detected in vivo by 1H-SRM, in cervical PGLs with SDHx mutations, at 3 months after EBR, reviewed by 2 independant experts blinded to all other clinical and genetics data.
Performance of cervical MRI at M3 and M12 after EBR
Reference diagnostic for response assessed by MRI at 3 months and 12 months after EBR: 1/ Complete response : tumour disappearance ; 2/ Partial response : decrease by at least 30% of tumour volume and no clinical symptomatology worsening ; 3/ stable : stability of tumour size and no clinical symptomatology worsening; 4/ Progression : increase by at least 20% of tumour volume and/or clinical symptomatological worsening
Performance of PET/CT at M12 after EBR
PERCIST criteria (PET response criteria in solid tumors) assessed by PET/CT at 3 months and 12 months after EBR
Metastatic evolution or death at M12
Occurence of an event related to the disease during 12 months follow-up (metastatic evolution of the disease or death). Metastases diagnostic is assessed remotely by presence in chromaffin tissue (http://www.sfendocrino.org/article/599/recommandations)
Full Information
NCT ID
NCT04583384
First Posted
October 5, 2020
Last Updated
December 20, 2021
Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Society for Endocrinology
1. Study Identification
Unique Protocol Identification Number
NCT04583384
Brief Title
In Vivo Succinate Detection After External Beam Radiation Therapy in SDHx- Paragangliomas
Acronym
RADIOSUCCES
Official Title
Evolution of Succinate Accumulation Detected in Vivo by Spectroscopic Magnetic Resonance Imaging (1H-SRM) After External Beam Radiation Therapy in SDHx-mutated Patients With Cervical Paragangliomas
Study Type
Interventional
2. Study Status
Record Verification Date
December 2021
Overall Recruitment Status
Recruiting
Study Start Date
October 27, 2020 (Actual)
Primary Completion Date
June 2022 (Anticipated)
Study Completion Date
June 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Society for Endocrinology
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
Qualitative and quantitative biomarker of response to radiotherapy is needed in paragangliomas. We aim at assessing the added value of 1H-SRM for the evaluation of early response to EBR therapy in patients with cervical SDHx PGL.
Detailed Description
Paragangliomas (PGL) are rare neuroendocrine tumors inherited in 40% of cases. SDHx genes (SDHA, SDHB, SDHC, SDHD), encoding the 4 subunits of the mitochondrial enzyme succinate dehydrogenase (SDH), are the most frequently involved.
Accumulation of succinate, the substrate for SDH, is a very specific biomarker for these mutations. Recently, we have demonstrated the feasability of detecting and quantifying succinate in tumors in vivo, by magnetic resonance spectroscopy (1H-SRM).
Patients carrying these mutations frequently develop cervical PGL for which the treatment of choice is external beam radiation therapy (EBR).
The objective of this project is to determine the feasibility of using 1H-SRM for the evaluation of early response to EBR therapy in patients with cervical SDHx PGL.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Paraganglioma of Head and Neck
Keywords
Paraganglioma,SDHx genes, 1H-Spectroscopy MRI
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
32 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Assigned Intervention
Arm Type
Other
Arm Description
Addition to the cervical angio-MRI, of a sequence of 1H-SRM 3T (SUCCESS) centered on the lesion studied, performed according to the following parameters: PRESS asymmetric monovoxel "PROBE", TE 144 ms, TR 2500 ms, 768 or 1024 medium.
Intervention Type
Diagnostic Test
Intervention Name(s)
1H-Spectroscopy MRI
Intervention Description
PRESS asymetric monovoxel " PROBE ", TE 144 ms, TR 2500 ms, 768 or 1024 averages
Primary Outcome Measure Information:
Title
Disappearance of succinate accumulation at M12
Description
Absence of succinate accumulation detected in vivo by 1H-SRM, in cervical PGLs with SDHx mutations, at 12 months after EBR, reviewed by 2 independant experts blinded to all other clinical and genetics data.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Disapperance of succinate accumulation at M3
Description
Absence of succinate accumulation detected in vivo by 1H-SRM, in cervical PGLs with SDHx mutations, at 3 months after EBR, reviewed by 2 independant experts blinded to all other clinical and genetics data.
Time Frame
3 months
Title
Performance of cervical MRI at M3 and M12 after EBR
Description
Reference diagnostic for response assessed by MRI at 3 months and 12 months after EBR: 1/ Complete response : tumour disappearance ; 2/ Partial response : decrease by at least 30% of tumour volume and no clinical symptomatology worsening ; 3/ stable : stability of tumour size and no clinical symptomatology worsening; 4/ Progression : increase by at least 20% of tumour volume and/or clinical symptomatological worsening
Time Frame
12 months
Title
Performance of PET/CT at M12 after EBR
Description
PERCIST criteria (PET response criteria in solid tumors) assessed by PET/CT at 3 months and 12 months after EBR
Time Frame
12 months
Title
Metastatic evolution or death at M12
Description
Occurence of an event related to the disease during 12 months follow-up (metastatic evolution of the disease or death). Metastases diagnostic is assessed remotely by presence in chromaffin tissue (http://www.sfendocrino.org/article/599/recommandations)
Time Frame
12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age ≥ 18 years
Signed informed consent
Patient with cervical PGL with planning of treatment with EBR
Patient with an SDHx mutation or unknown genetic status
Patient affiliated to a social security scheme
Exclusion Criteria:
Pregnant woman
Contraindication to MRI (implantable device, etc.)
Impossibility of lying down without movement for 45 minutes (hyperalgesic patient, claustrophobia, etc.)
PPGL having previously been the subject of local (excluding surgery) or systemic treatment
PPGL <1 cm longest axis
Patient under guardianship or curatorship
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Charlotte LUSSEY-LEPOUTRE, PhD
Phone
+33142178370
Email
charlotte.lussey@inserm.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Malha BERRAH, MSc
Phone
+33156095822
Email
malha.berrah@aphp.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Laurence AMAR, PhD
Organizational Affiliation
Hôpital Européen Georges-Pompidou
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hôpital Lariboisière
City
Paris
ZIP/Postal Code
75010
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Philippe HERMAN, Dr
Phone
+33147711111
Email
philippe.herman@aphp.fr
Facility Name
Hôpital Pitié-Salpêtrière
City
Paris
ZIP/Postal Code
75013
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Charlotte LUSSEY-LEPOUTRE, Dr
Phone
+33142178370
Email
charlotte.lussey@inserm.fr
Facility Name
Hopital européen Georges Pompidou
City
Paris
ZIP/Postal Code
75015
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Laurence AMAR, PhD
Phone
+33156093771
Email
laurence.amar@aphp.fr
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
Individual participant data (IPD) that underlie results in publication could be shared.
IPD Sharing Time Frame
Two years after the last publication
IPD Sharing Access Criteria
Data sharing must be accepted by the sponsor and the PI based on scientific project and scientific involvement of the PI team.
Teams wishing obtain IPD must meet the sponsor and IP team to present scientifics (and commercial) purpose, IPD needed, format of data transmission, and timeframe. Technical feasibility and financial support will be discussed before mandatory contractualization
Learn more about this trial
In Vivo Succinate Detection After External Beam Radiation Therapy in SDHx- Paragangliomas
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