OpenOnco · Meningioma - resection plus adjuvant RT review
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OpenOnco · Treatment Plan
Treatment plan — Meningioma
PLAN-COVERAGE-MENINGIOMA-001-V1 · v1 · 2026-06-27
Patient
COVERAGE-MENINGIOMA-001 · Algorithm: ALGO-MENINGIOMA-1L
DiagnosisMeningioma
MOH / ICD-10D32
ICD-O-39530/0; C70

Clinical significance of mutations (ESCAT)

Tumor-board context — the engine does not use these tiers to rank tracks
BiomarkerVariantESCATEvidenceClinical significanceDrugsSources
BIO-NF2-GERMLINENF2 germline pathogenic (merlin/schwannomin loss-of-function)IIA
  • SRC-NCCN-CNS-2025
Evidence cited from clinical guidelines; per-source evidence levels not yet structured. See Phase-2-of-CIViC-pivot for re-cite roadmap.
NF2 germline pathogenic variants drive Neurofibromatosis Type 2 (NF2 / NF2- related schwannomatosis) — characterized by bilateral vestibular schwannomas, meningiomas (often multiple), spinal schwannomas, ependymomas, and juvenile posterior subcapsular cataract. Confirmed-carrier surveillance protocol (per NCCN CNS / Manchester NF2 Consensus): brain MRI with contrast (thin slices through IAC) starting at age 10-12 (earlier if symptomatic) q1-2y for vestibular schwannoma and intracranial meningioma, whole-spine MRI q2-3y for spinal schwannomas and meningiomas, annual neurological exam, annual audiology (pure-tone + speech discrimination + ABR), ophthalmology exam q1-2y. Bevacizumab is active for growing or symptomatic vestibular schwannoma (hearing preservation / volume reduction in ~40-60% per Plotkin et al.) — surveillance-triggered, not prophylactic. Surgery + radiosurgery remain mainstays for accessible lesions; radiosurgery use is cautious due to malignant transformation risk in NF2. ESCAT IIA.bevacizumab 5-7.5 mg/kg q2-3w — growing or symptomatic vestibular schwannoma in NF2 (off-label, evidence-supported per Plotkin et al. 2012)
stereotactic radiosurgery — selected vestibular schwannomas, cautious (malignant transformation risk in NF2)
microsurgical resection — symptomatic / brainstem-compressing schwannomas, meningiomas
multidisciplinary NF2 clinic (otology, neurosurgery, neuro-oncology, genetics)
  • SRC-NCCN-CNS-2025
BIO-NF2NF2 loss-of-function (biallelic somatic in sporadic meningioma ~50%; germline in NF2 syndrome); merlin loss by IHC acceptable surrogateIIIA
Standard care
  • SRC-NCCN-CNS-2025: Level Category 2B (Supports, Sensitivity/Response)
Resistance or avoidance signal
  • SRC-EANO-MENINGIOMA-2024: Level B ⚠ Resistance
NF2 loss is the most common molecular driver in meningioma (~50% of grade I; higher proportion in grade II/III). Despite its frequency, no FDA/EMA-approved targeted therapy exists specifically for NF2-mutant meningioma as of 2026. Standard treatment is maximal safe surgical resection ± radiotherapy (SRS for small residual, fractionated RT for larger/grade II-III). Systemic therapy evidence for progressive/recurrent meningioma: Selumetinib (MEK inhibitor; FDA-approved for NF1 pediatric plexiform neurofibroma): investigated in NF2-related vestibular schwannomas (ACTR-4 trial) and NF2-related meningiomas — limited hearing preservation benefit; single-agent activity modest. Bevacizumab (anti-VEGF): off-label use in progressive grade II-III meningioma or NF2-related schwannomas — radiologic responses in 40–50% in retrospective series, PFS benefit uncertain. AKT1 E17K-mutant meningioma (~10% of grade I): AKT inhibitors (capivasertib, ipatasertib) in phase II trials — not NF2-specific but relevant for co-occurring pathway alterations. SMO-mutant (~5% of meningioma): vismodegib case reports show activity. ESCAT IIB: NF2 loss is molecularly relevant but no validated targeted therapy with prospective trial data.bevacizumab 7.5–10 mg/kg IV q3w — off-label for progressive grade II-III meningioma or NF2 syndrome-related tumors; radiologic responses in ~40–50% retrospective series
selumetinib 25 mg/m² PO BID — investigational for NF2-related schwannomas (ACTR-4 regimen); not standard for meningioma
  • SRC-EANO-MENINGIOMA-2024
  • SRC-NCCN-CNS-2025

Primary current-line option

Local therapy plan
★ DEFAULT
Indication
IND-MENINGIOMA-1L-RESECTION-RT
Regimen
Reason
Primary current-line option selected by ALGO-MENINGIOMA-1L at step 1.

Pre-treatment investigations

Investigations before treatment start · critical / standard / desired · merged across tracks
IDNamePriorityCategoryWhere to orderNeeded for
TEST-CBCComplete Blood Count with DifferentialCriticallaball tracks
TEST-CMPComprehensive Metabolic PanelCriticallaball tracks
TEST-LFTLiver Function Tests (ALT, AST, bilirubin, ALP, GGT, albumin)Criticallaball tracks
TEST-BRAIN-MRI-CONTRASTBrain MRI with contrastStandardall tracks

What NOT to do

Explicit prohibitive rules, each grounded in a regimen / supportive care / contraindication entity
Local therapy plan (IND-MENINGIOMA-1L-RESECTION-RT)
  • Do not offer systemic therapy as default first-line treatment for resectable or radiation-manageable meningioma.
  • Do not pursue gross total resection at the cost of unacceptable neurologic morbidity; maximal safe resection is the target.
  • Do not omit postoperative pathology grade, brain invasion assessment, and residual-disease MRI before deciding on adjuvant RT.

MDT brief

Data quality

Complete for MDT review. Required MDT data checks are complete for the current case profile.
  • Biomarker coverage: 0/0 known (100%), 0 missing, 0 default-track gaps
Technical MDT skill metadata (0/16 activated in this plan)
All registered virtual specialists. ✓ — activated for this case; ○ — not activated (available for other clinical scenarios).
Specialistskill_idVersionLast reviewedSign-offsDomain
Cellular therapy specialist (CAR-T)cellular_therapy_specialistv0.1.02026-04-250cellular_therapy
Clinical pharmacistclinical_pharmacistv0.1.02026-04-250clinical_pharmacy
Hematologist / oncohematologisthematologistv0.1.02026-04-250hematology_oncology
Hematopathologist (lymphoma / leukemia / myeloma)hematopathologistv0.1.02026-04-250hematopathology
Infectious disease / hepatologyinfectious_disease_hepatologyv0.1.02026-04-250infectious_diseases
Medical oncologist (solid-tumor chemotherapist)medical_oncologistv0.1.02026-04-250solid_oncology
Molecular geneticist / molecular oncologistmolecular_geneticistv0.1.02026-04-250molecular_oncology
Palliative carepalliative_carev0.1.02026-04-250palliative_care
Pathologist (general)pathologistv0.1.02026-04-250pathology
Primary care / family physicianprimary_carev0.1.02026-04-250primary_care
Psycho-oncologistpsychologistv0.1.02026-04-250psychosocial
Radiation oncologistradiation_oncologistv0.1.02026-04-250radiation_oncology
Radiologistradiologistv0.1.02026-04-250diagnostic_imaging
Social worker / case managersocial_worker_case_managerv0.1.02026-04-250psychosocial
Surgical oncologistsurgical_oncologistv0.1.02026-04-250surgical_oncology
Transplant specialist (BMT)transplant_specialistv0.1.02026-04-250cellular_therapy

Sources cited

Experimental options (clinical trials)

Third plan track — open-enrollment trials from ClinicalTrials.gov. Render-time metadata; engine selection is not affected by this block (CHARTER §8.3). Last synced: 2026-06-27.
NCTTitlePhaseStatusSponsorUASignalsEligibility (excerpt)
NCT05895344Long-term Cognitive and Functional Impact of Proton-therapy or Modern Fractionated Radiotherapy in Cavernous Sinus Meningioma: An Open-label Randomized 1:1 Phase III StudyNARECRUITINGCentre Francois BaclesseSingle country
NCT05254197SeOuL cOhort of Brain Tumor MONitoring Study (SOLOMON)N/ARECRUITINGSeoul National University HospitalSingle country
NCT06650163Zr-89 Crefmirlimab Berdoxam and Immuno-Positron Emission Tomography for the Imaging of Patients With Resectable Brain TumorsPHASE1RECRUITINGJonsson Comprehensive Cancer CenterPhase 1 only Small N (<50) Single country
NCT06710249Impact of Salovum® and SPC® Flakes on Brain Tumor Induced EdemaPHASE2RECRUITINGPeter SiesjöSmall N (<50) Single country
NCT04638478PREselection of Patients at Risk for COgnitive DEcline After Radiotherapy Using Advanced MRIN/ARECRUITINGMaastricht Radiation OncologySurrogate endpoint only Single country
NCT07044076Translation and Validation of the MQOL Self-questionnaire Into French for Assessing Quality of Life in Patients With MeningiomasN/ARECRUITINGCentre Hospitalier St AnneSingle country
NCT06607692Study in Children and Adolescents of 177Lu-DOTATATE (Lutathera®) Combined With the PARP Inhibitor Olaparib for the Treatment of Recurrent or Relapsed Solid Tumours Expressing Somatostatin Receptor (SSTR) (LuPARPed).PHASE1 / PHASE2RECRUITINGFundación de investigación HMSmall N (<50) Single country
NCT03702309Liquid Biopsy Evaluation and Repository Development at Princess MargaretN/ARECRUITINGUniversity Health Network, TorontoSingle country
NCT04427384Registry of Patients With Brain Tumors Treated With STaRT (GammaTiles)N/ARECRUITINGGT Medical Technologies, Inc.Single country
NCT05793034Predictive Factors for Survival in Aggressive MeningiomasNARECRUITINGFondazione Policlinico Universitario Agostino Gemelli IRCCSSingle country

Verify recruitment status directly with the trial site. ctgov data can lag behind current UA-site status.

Option availability in Ukraine

Per-track UA registration · NSZU · cost · access pathway. Render-time metadata; engine selection does not depend on these fields (CHARTER §8.3).
OptionUA registrationNSZUCost orientationAccess pathway
Local therapy plan
No regimen components on this track — availability unknown
— unknown— unknown₴-? — verify pathwaynot recorded
Trial · 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 UA site listed — international referral required
— unknown— unknown
self-pay: ₴0/course
Trial sponsor
Trial · NCT05254197
SeOuL cOhort of Brain Tumor MONitoring Study (SOLOMON)
No UA site listed — international referral required
— unknown— unknown
self-pay: ₴0/course
Trial sponsor
Trial · NCT06650163
Zr-89 Crefmirlimab Berdoxam and Immuno-Positron Emission Tomography for the Imaging of Patients With Resectable Brain Tumors
No UA site listed — international referral required
— unknown— unknown
self-pay: ₴0/course
Trial sponsor
Trial · NCT06710249
Impact of Salovum® and SPC® Flakes on Brain Tumor Induced Edema
No UA site listed — international referral required
— unknown— unknown
self-pay: ₴0/course
Trial sponsor
Trial · NCT04638478
PREselection of Patients at Risk for COgnitive DEcline After Radiotherapy Using Advanced MRI
No UA site listed — international referral required
— unknown— unknown
self-pay: ₴0/course
Trial sponsor
Trial · NCT07044076
Translation and Validation of the MQOL Self-questionnaire Into French for Assessing Quality of Life in Patients With Meningiomas
No UA site listed — international referral required
— unknown— unknown
self-pay: ₴0/course
Trial sponsor
Trial · NCT06607692
Study in Children and Adolescents of 177Lu-DOTATATE (Lutathera®) Combined With the PARP Inhibitor Olaparib for the Treatment of Recurrent or Relapsed Solid Tumours Expressing Somatostatin Receptor (SSTR) (LuPARPed).
No UA site listed — international referral required
— unknown— unknown
self-pay: ₴0/course
Trial sponsor
Trial · NCT03702309
Liquid Biopsy Evaluation and Repository Development at Princess Margaret
No UA site listed — international referral required
— unknown— unknown
self-pay: ₴0/course
Trial sponsor
Trial · NCT04427384
Registry of Patients With Brain Tumors Treated With STaRT (GammaTiles)
No UA site listed — international referral required
— unknown— unknown
self-pay: ₴0/course
Trial sponsor
Trial · NCT05793034
Predictive Factors for Survival in Aggressive Meningiomas
No UA site listed — international referral required
— unknown— unknown
self-pay: ₴0/course
Trial sponsor

Cost information is orientation. Verify with a specific pharmacy / foundation / trial site. Status updated: 2026-06-27.