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
Condition(s) studied
Investigational drug(s) / intervention(s)
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
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)
| Facility | City | Region | Status |
|---|---|---|---|
| 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 |
More Centre Francois Baclesse trials in France
Other trials for the same condition
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