Ireland
--:--IST
Recruiting Not applicable

Long-term Cognitive and Functional Impact of Proton-therapy or Modern Fractionated Radiotherapy in Cavernous Sinus Meningioma: An Open-label Randomized 1:1 Phase III Study

NCT05895344 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2024-02-26
Last updated
2025-09-29

Condition(s) studied

Cavernous Sinus MeningiomaProton-therapyPhoton RadiotherapyCognitive Impairment

Investigational drug(s) / intervention(s)

Proton-therapyPhoton radiotherapy

Proton-therapy: Proton pencil-beam-scanning irradiation (50,4 Gy (RBE) in 28 fractions)

Photon radiotherapy: Intensity modulated radiotherapy with or without stereotactic positioning (50,4 Gy in 28 fractions)

Study summary

Cavernous sinus meningiomas are close to optic nerve, pituitary gland, cranial nerve, and hippocampi.

The doses delivered to these structures are crucial and radiotherapy of cavernous sinus meningiomas exposes patients to late secondary effects (pituitary deficit, nerve palsy, cognitive impairment…). In 2012, Gondi reported that a dose given to 40% of the bilateral hippocampi greater than 7.3 Gy is associated with long-term impairment in list-learning delayed recall after FSRT for benign or low-grade adult brain tumors.

There is no published or recruiting prospective study evaluating the impact of proton-therapy or conventional irradiation on neurocognitive function for meningioma patients. Notably, long-term cognitive or ocular impact of these modern irradiation schemes remains poorly known. Yet, these patients had a long life-expectancy, and are at risk of developing long-term sequelae. Thus, according to its ballistic advantage, an improvement of patient functional outcomes and a reduction of neurocognitive long-term toxicity are expected if tissue sparing proton-therapy is used.

In this context, a randomized prospective study, evaluating long-term toxicity of these two irradiation modalities (Proton Therapy (PRT) and photon radiotherapy (XRT)) seems crucial to further assess proton-therapy indication for these patients.

Although literature reports excellent outcomes for intracranial meningioma patients treated by proton-therapy, none of the eight retrospective studies found in the literature used an accurate and full evaluation of long-term toxicity

Eligibility

Sex
ALL
Min age
18 Years
Max age
70 Years
Healthy volunteers
No
Inclusion Criteria: * Cavernous sinus meningioma for which clinical target volume is larger than 3 centimeters * Anterior skull base meningioma, invading by contiguity the cavernous sinus can be included * Histologic proven Grade I meningioma * Meningioma for which biopsy is not safely achievable and for which growing and imaging criteria are in favour of grade I meningioma can be included * Age \>18 years and ≤70 years * Indication of irradiation validated by a pluridisciplinary meeting * Adjuvant or exclusive irradiation is allowed. * Use of conventional fractionation: 1.8Gy (RBE)/fraction * Signed informed consent form * WHO Performance status equal to 0 or 1 * Patient affiliated to the French social health insurance * MoCA score ≥ cut-off of GRECOGVASC normative data (Roussel, 2016, cf annexe 1) * Patient whose neuropsychological abilities allow to follow the requirements of the protocol Exclusion Criteria: * Patient with mutation in a known predisposition gene (NF-2, SMARCE-1…) * Cerebrovascular pathology, presence of other tumors of the nervous system, congenital malformations of the nervous system, multiple sclerosis, Parkinson's disease and other dementias, organic psychosis (other than dementia), schizophrenia, and neurodegenerative disease * Radiosurgery, hypofractionated regimen * Other localization than cavernous sinus * Histologic proven Grade II or III meningioma * Patient with unadjusted antiepileptic drug * Contraindication to MRI * Patient with a history of brain irradiation * Patient with a history of cancer in the last five years (excluding skin baso-cellular carcinoma) * Pregnant/breastfeeding woman * Any geographical conditions, social and associated psychopathology that may compromise the patient's ability to participate in the study * Participation in a therapeutic trial for less than 30 days * Patient deprived of freedom or under guardianship

Primary outcome measure(s)

  • functional deterioration evaluated by individual neurocognitive test scores — 5 years
    Neurocognitive deterioration defined as the occurrence of cognitive impairment (a total of 5 impaired z-scores (17 z-scores for 6 different tests)

Trial sites (13)

FacilityCityRegionStatus
Centre Francois Baclesse Caen France Recruiting
Hopital d'Instruction des Armées PERCY Clamart France Not Yet Recruiting
CHU Grenoble-Alpes Grenoble France Not Yet Recruiting
Centre Guillaume le Conquerant Le Havre France Not Yet Recruiting
Centre Léon Bérard Lyon France Not Yet Recruiting
Hospices civils de Lyon Lyon France Not Yet Recruiting
Centre Antoine Lacassagne Nice France Not Yet Recruiting
Hôpital Pitié Salpétrière Paris France Not Yet Recruiting
Institut Curie Paris France Recruiting
Institut Curie Saint-Cloud France Not Yet Recruiting
Centre Paul Strauss Strasbourg France Not Yet Recruiting
IUCT Toulouse France Recruiting
Gustave Rousy Villejuif France Not Yet Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05895344 on ClinicalTrials.gov ↗ ← All trials in France