Condition: Cavernous Sinus Meningioma · Proton-therapy · Photon Radiotherapy · Sponsor: Centre Francois Baclesse
Interested? Contact the study team ↓
Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.
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…
This description comes directly from the study's public registry record.
Jeanne RIVERAIN, MD · +33 2 31 45 50 50 · j.riverain@baclesse.unicancer.fr
Jean-Michel GRELLARD · +33 2 31 45 50 50 · jm.grellard@baclesse.unicancer.fr
There is no obligation to join — the study team can answer your questions about taking part.
Always discuss trial participation with your own doctor first.
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
Reproduced word-for-word from the public registry record — the study team can answer questions about it.
| 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 |
+ 1 more locations — full list on the registry record.
This study lists sites in the areas below. Each link shows other recruiting studies near that city, from the public registry record.
Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.
We email about this public record only. Unsubscribe anytime with one click. Never medical advice. By subscribing you agree to our Terms of Use and Privacy Policy.