Actively Recruiting
Combination of Everolimus and 177Lu-DOTATATE in the Treatment of Grades 2 and 3 Refractory Meningioma: a Phase IIb Clinical Trial
Led by Central Hospital, Nancy, France · Updated on 2025-03-11
28
Participants Needed
2
Research Sites
178 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Meningioma, the most common intracranial primary tumor of the central nervous system predominantly affects people in their fifties. Meningiomas are generally subdivided into two entities: a priori non-aggressive meningiomas (grade 1), and meningiomas at high risk of aggressive behavior (grade 2/atypical and 3/anaplastic). The current conventional treatments for meningioma are surgery and radiotherapy. When these treatments are no longer feasible, meningiomas are considered refractory irrespectively of grade, and in these rare entities, the therapeutic arsenal is reduced to the few treatments that have shown limited efficacy. Refractory, and particularly grades 2 and 3 meningiomas, have very poor prognoses with a progression-free survival at 6 months (PFS-6) of 26%. The European Response Assessment in Neuro-Oncology group (RANO) recommends that in any new, grades 2 and 3 meningioma, therapy that achieves a PFS-6 \>30% in phase II trials be considered promising. In Nuclear Medicine, Peptide Receptor Radionuclide Therapy (PRRT) with 177Lu-DOTATATE, currently used on a compassionate basis in refractory meningioma, deploys an octreotide-like effect, and appears very promising, with preliminary PFS-6 of 94% and an overall survival at 12 months (OS-12) of 88% in grade 1 meningioma. However, its PFS-6 is reduced to 28% with an OS-12 of 65% in WHO grades 2 and 3 meningioma. Recently the non-radiolabeled octreotide and everolimus combination however achieved a PFS-6 of 55% and an OS-12 of 75% in a population of 90% WHO grades 2 and 3 meningioma.
CONDITIONS
Official Title
Combination of Everolimus and 177Lu-DOTATATE in the Treatment of Grades 2 and 3 Refractory Meningioma: a Phase IIb Clinical Trial
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patient younger than 80 years old who has received full information about the trial and signed consent
- Eligible for compassionate access program to Lutathera treatment
- WHO performance status of 3 or less
- Diagnosed with grade 2 or 3 meningioma confirmed by histology, not suitable for surgery or radiotherapy, with clinical or radiological progression
- Clinical worsening or at least 10% tumor growth within 6 months
- Tumor expresses somatostatin receptors shown by 68Ga-DOTATOC PET with lesion uptake equal or above liver uptake or 1.7 times the opposite meninges
- Had brain MRI and 68Ga-DOTATOC PET within past 2 months
- Effective contraception for women of childbearing age
- Has social security coverage
You will not qualify if you...
- Allergy or hypersensitivity to everolimus
- Contraindications to 177Lu-DOTATATE including kidney failure (GFR below 40 mL/min/1.73m2), severe liver failure (bilirubin over 3 times normal), or severe heart failure (NYHA class III or IV)
- Current treatment with other rapamycin derivatives or immunosuppressants
- Taking strong CYP3A4 or P-glycoprotein inhibitors or inducers such as ketoconazole, itraconazole, posaconazole, voriconazole, telithromycin, clarithromycin, nefazodone, ritonavir, atazanavir, saquinavir, darunavir, indinavir, or nelfinavir
- Concurrent use of certain CYP3A4 substrates with narrow therapeutic index without close monitoring
- Unable to have MRI or 68Ga-DOTATOC PET/CT scans
- Under psychiatric care as defined by French law
- Women of childbearing age without effective contraception
- Unable to attend follow-up visits for 12 months
- Currently participating in another interventional clinical research trial
- Pregnant, giving birth, or breastfeeding
- Minor without emancipation
- Under legal protection measures like guardianship
- Unable to give informed consent
AI-Screening
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Trial Site Locations
Total: 2 locations
1
CHRU of Nancy
Vandœuvre-lès-Nancy, Grand Est, France, 54511
Not Yet Recruiting
2
Nancy Hospital
Vandœuvre-lès-Nancy, France, 54511
Actively Recruiting
Research Team
A
Antoine VERGER, MD,PhD
CONTACT
C
Caroline BOURSIER, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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