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Recruiting NCT05895344

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

No phase Interventional Cavernous Sinus Meningioma Proton-therapy Photon Radiotherapy Cognitive Impairment

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Proton-therapy, Photon radiotherapy.
Who it may be relevant to
Registry conditions: Cavernous Sinus Meningioma, Proton-therapy, Photon Radiotherapy, Cognitive Impairment. Basic parameters: 18 years — 70 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Long-term Cognitive and Functional Impact of Proton-therapy or Modern Fractionated Radiotherapy in Cavernous Sinus Meningioma

Overview

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

Interventions

  • Radiation Proton-therapy
    Proton pencil-beam-scanning irradiation (50,4 Gy (RBE) in 28 fractions)
  • Radiation Photon radiotherapy
    Intensity modulated radiotherapy with or without stereotactic positioning (50,4 Gy in 28 fractions)

Primary outcome measures

  • functional deterioration evaluated by individual neurocognitive test scores [Time frame: 5 years]

Eligibility criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Treatment

Study locations

France · 13 centers
  • Centre Francois Baclesse — Caen
  • Hopital d'Instruction des Armées PERCY — Clamart
  • CHU Grenoble-Alpes — Grenoble
  • Centre Guillaume le Conquerant — Le Havre
  • Centre Léon Bérard — Lyon
  • Hospices civils de Lyon — Lyon
  • Centre Antoine Lacassagne — Nice
  • Hôpital Pitié Salpétrière — Paris
  • … and 5 more centers

Publications

  • Lesueur P, Clarisse B, Lequesne J, Licaj I, Feuvret L, Stefan D, Ricard D, Noel G, Balosso J, Lange M, Capel A, Durand-Zaleski I, Castera M, Legrand B, Goliot N, Hedou C, Grellard JM, Valable S. Proton therapy versus conventional radiotherapy for the treatment of cavernous sinus benign meningioma, a randomized controlled phase III study protocol (COG-PROTON-01). BMC Cancer. 2024 Dec 30;24(1):1594. PMID 39736544

Identifiers

NCT: NCT05895344 · 2023-A00401-44

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗