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In Vivo Succinate Detection After External Beam Radiation Therapy in SDHx- Paragangliomas

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04583384
Acronym
RADIOSUCCES
Enrollment
32
Registered
2020-10-12
Start date
2020-10-27
Completion date
2025-06-30
Last updated
2021-12-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Paraganglioma of Head and Neck

Keywords

Paraganglioma,SDHx genes, 1H-Spectroscopy MRI

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.

Interventions

DIAGNOSTIC_TEST1H-Spectroscopy MRI

PRESS asymetric monovoxel PROBE , TE 144 ms, TR 2500 ms, 768 or 1024 averages

Sponsors

Society for Endocrinology
CollaboratorOTHER
Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Disappearance of succinate accumulation at M1212 monthsAbsence 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

MeasureTime frameDescription
Disapperance of succinate accumulation at M33 monthsAbsence 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 EBR12 monthsReference 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 EBR12 monthsPERCIST criteria (PET response criteria in solid tumors) assessed by PET/CT at 3 months and 12 months after EBR
Metastatic evolution or death at M1212 monthsOccurence 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)

Countries

France

Contacts

Primary ContactCharlotte LUSSEY-LEPOUTRE, PhD
charlotte.lussey@inserm.fr+33142178370
Backup ContactMalha BERRAH, MSc
malha.berrah@aphp.fr+33156095822

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026