OpenOnco · DIS-GBM · High-risk biology / bulky disease
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OpenOnco · Treatment Plan
Treatment plan — Glioblastoma
PLAN-VAR-GBM-HIGHRISK-V1 · v1 · 2026-05-13
Patient
VAR-GBM-HIGHRISK · Algorithm: ALGO-GBM-NEWLY-DIAGNOSED-1L
DiagnosisGlioblastoma
MOH / ICD-10C71
ICD-O-39440/3; C71

Clinical significance of mutations (ESCAT)

Tumor-board context — the engine does not use these tiers to rank tracks
✅ Covered biomarkers (matched in KB)
BiomarkerVariantESCATEvidenceClinical significanceDrugsSources
No clinically actionable variants matched in this profile.
⚠️ Not included in plan
BiomarkerStatus
BIO-MGMT-METHYLATIONBIO definition in KB; no ESCAT BMA entry — verify with clinician

Primary current-line option

Standard plan
★ DEFAULT
Indication
IND-GBM-NEWLY-DIAGNOSED-STUPP
Regimen
Stupp protocol — Temozolomide concurrent + adjuvant
Drugs + NSZU
  • Temozolomide (DRUG-TEMOZOLOMIDE) Concurrent: 75 mg/m² PO daily during RT 6 weeks; Adjuvant: 150 mg/m² PO days 1-5 cycle 1 (escalate to 200 if tolerated) every 28 days × 6 cycles · Concurrent daily × 42 days then 4-week break then adjuvant cycles 1-6 · PO ✓ NSZU covered
Reason
Provisional current-line default from ALGO-GBM-NEWLY-DIAGNOSED-1L: step 1 did not select a treatment branch. IDH-mutant glioma grade 4: not GBM per WHO 2021. Manage as astrocytoma IDH-mutant (vorasidenib INDIGO). Separate disease pathway.

Other current-line alternatives (2 tracks)

Same treatment line; review when biomarker, access, contraindication, or patient-context assumptions change.
Standard plan
Indication
IND-GBM-NEWLY-DIAGNOSED-ELDERLY-TMZ
Regimen
Temozolomide monotherapy
Drugs + NSZU
  • Temozolomide (DRUG-TEMOZOLOMIDE) ✓ NSZU covered
Reason
Current-line alternative presented for HCP consideration
Standard plan
Indication
IND-GBM-NEWLY-DIAGNOSED-ELDERLY-HYPORT
Regimen
Hypofractionated radiotherapy for GBM
Reason
Current-line alternative presented for HCP consideration

Pre-treatment investigations

Investigations before treatment start · critical / standard / desired · merged across tracks
IDNamePriorityCategoryWhere to orderNeeded for
TEST-IDH-MUTATIONIDH1/IDH2 mutationCriticalhistologyCSD Lab ✓ (code TBC)all tracks
TEST-MGMT-METHYLATIONMGMT methylationCriticalhistologyCSD Lab ✓ (code TBC)all tracks
TEST-MRI-BRAIN-CONTRASTMRI brain with contrastStandardimagingall tracks
TEST-NGS-COMPREHENSIVEComprehensive NGS tumor panel (DNA + RNA, ≥300 genes)DesiredhistologyCSD Lab: M065desired (standard)

Red flags — PRO / CONTRA aggressive

PRO-AGGRESSIVE

Triggers that push toward the aggressive track
  • Symptomatic raised intracranial pressure / mass effect in glioblastoma: declining GCS, new focal deficit, papilledema, midline shift on imaging, or seizure cluster. Mandates immediate neurosurgical / corticosteroid intervention BEFORE oncologic systemic therapy. RF-GBM-INTRACRANIAL-PRESSURE-EMERGENCY
  • Glioblastoma progression on or after first-line Stupp regimen: MRI evidence of true progression (RANO criteria — distinguished from pseudoprogression by serial imaging / advanced techniques), early recurrence <6 months post-RT (often pseudoprogression — repeat MRI at 4-8 weeks before re-treatment decision), or distant new lesion. Routes from upfront Stupp to recurrent-GBM algorithm (re-resection + bevacizumab / TTF / regorafenib / lomustine / re-irradiation). RF-GBM-TRANSFORMATION-PROGRESSION

CONTRA-AGGRESSIVE

Hard contraindications to escalation

What NOT to do

Explicit prohibitive rules, each grounded in a regimen / supportive care / contraindication entity
Standard plan (IND-GBM-NEWLY-DIAGNOSED-STUPP)
  • Do NOT delay starting RT beyond 6 weeks post-resection
  • Do NOT skip MGMT testing — defines elderly (≥70) regimen choice
  • Do NOT skip PJP prophylaxis (universal lymphopenia → opportunistic infection)
  • Do NOT use enzyme-inducing AEDs (phenytoin, carbamazepine) — accelerate TMZ clearance; use levetiracetam
Standard plan (IND-GBM-NEWLY-DIAGNOSED-ELDERLY-TMZ)
  • Do NOT use TMZ alone in MGMT-unmethylated GBM ≥70 — minimal benefit; prefer hypofractionated RT
  • Do NOT use full Stupp (60 Gy/30 fx) in patients ≥70 or KPS <60 — excessive toxicity
  • Do NOT skip MGMT testing before choosing TMZ vs RT — this is the key biomarker in elderly
  • Do NOT skip PJP prophylaxis (co-trimoxazole) — lymphopenia risk applies to TMZ mono too
Standard plan (IND-GBM-NEWLY-DIAGNOSED-ELDERLY-HYPORT)
  • Do NOT use full Stupp 60 Gy/30 fx in patients ≥70 or KPS <60 — unacceptable toxicity in elderly
  • Do NOT omit TMZ without first checking MGMT status — methylated patients benefit significantly
  • Do NOT skip MGMT testing — drives concurrent TMZ decision
  • Do NOT start RT without post-resection MRI (within 48h of surgery)
  • Do NOT delay RT beyond 6 weeks post-surgery

Timeline

Treatment timeline — derived from regimen + monitoring schedule

Standard plan

Induction · Stupp protocol — Temozolomide concurrent + adjuvant
28-day cycles × Concurrent phase 6 weeks + adjuvant 6 cycles (~7 months total)

Standard plan

Induction · Temozolomide monotherapy
28-day cycles × Until progression or unacceptable toxicity; schedule per GBM protocol

MDT brief

MDT talk tree (2 steps)

#OwnerTopicAction
1molecular_geneticistSpecialist review Indication references an actionable genomic biomarker — mutation / target / actionability interpretation needed.
2radiologistSpecialist review Imaging findings present — radiologist needed for staging/restaging.

Skills (recommended) — for consideration (2)

  • Molecular geneticist / molecular oncologist recommended
    Indication references an actionable genomic biomarker — mutation / target / actionability interpretation needed.
  • Radiologist recommended
    Imaging findings present — radiologist needed for staging/restaging.

Data quality

Usable with caveats. No critical default-track gap was found, but the MDT should review the listed caveats before final sign-off.
  • Biomarker coverage: 1/1 known (100%), 0 missing, 0 default-track gaps
  • Unevaluated RedFlags: RF-GBM-FRAILTY-AGE, RF-GBM-HIGH-RISK-BIOLOGY, RF-GBM-INFECTION-SCREENING, RF-GBM-INTRACRANIAL-PRESSURE-EMERGENCY, RF-GBM-TRANSFORMATION-PROGRESSION
Technical MDT skill metadata (2/16 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: 2026-05-13.
NCTTitlePhaseStatusSponsorUASignalsEligibility (excerpt)
NCT05768087Escalated Dose Proton Therapy Within the Multimodality Treatment of Glioblastoma PatientsNARECRUITINGUniversity of AarhusSmall N (<50) Single country
NCT06146738The PALSUR-study: Palliative Care Versus Surgery in High-grade Glioma Patients (ENCRAM 2203)N/ARECRUITINGJasper Gerritsen
NCT06001281Predictive Value of Soluble CD146 in Glioblastoma PatientsNARECRUITINGAssistance Publique Hopitaux De MarseilleSurrogate endpoint only Single country
NCT07003542A Phase 2 and Pharmacodynamic Study of Sitagliptin in Patients With Progressive Grade 4 GliomasPHASE2RECRUITINGCase Comprehensive Cancer CenterSmall N (<50) Single country
NCT06419946Lomustine in Addition to Standard of Care in Patients With MGMT Methylated GlioblastomaPHASE3RECRUITINGVastra Gotaland Region
NCT03672721IA Carboplatin + Radiotherapy in Relapsing GBMPHASE1 / PHASE2RECRUITINGUniversité de SherbrookeSmall N (<50) Single country
NCT07209241Different Approaches for CART-EGFR-IL13Ra2 Dosing in Recurrent GBMPHASE1RECRUITINGUniversity of PennsylvaniaPhase 1 only Small N (<50) Single country
NCT05734560D2C7-IT and 2141-V11 in Newly Diagnosed GBM PatientsPHASE1 / PHASE2RECRUITINGDarell BignerSingle country
NCT06418113Neoadjuvant Radio-chemotherapy Safety Pilot Study in Patients With GlioblastomaPHASE1RECRUITINGHospital San Carlos, MadridPhase 1 only Small N (<50) Single country
NCT06047379Safety and Efficacy of NEO212 in Patients With Astrocytoma IDH-mutant, Glioblastoma IDH-wildtype or Brain MetastasisPHASE1 / PHASE2RECRUITINGNeonc Technologies, Inc.Surrogate endpoint only Single 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
Standard plan
Stupp protocol — Temozolomide concurrent + adjuvant (REG-STUPP-TMZ)
✓ registered✓ covered₴-? — verify pathwayNSZU formulary
Standard plan
Temozolomide monotherapy (REG-TMZ-MONO)
✓ registered✓ covered₴-? — verify pathwayNSZU formulary
Standard plan
Hypofractionated radiotherapy for GBM (REG-HYPOFRACTIONATED-RT-GBM)
No regimen components on this track — availability unknown
— unknown— unknown₴-? — verify pathwaynot recorded
Trial · NCT05768087
Escalated Dose Proton Therapy Within the Multimodality Treatment of Glioblastoma Patients
No UA site listed — international referral required
— unknown— unknown
self-pay: ₴0/course
Trial sponsor
Trial · NCT06146738
The PALSUR-study: Palliative Care Versus Surgery in High-grade Glioma Patients (ENCRAM 2203)
No UA site listed — international referral required
— unknown— unknown
self-pay: ₴0/course
Trial sponsor
Trial · NCT06001281
Predictive Value of Soluble CD146 in Glioblastoma Patients
No UA site listed — international referral required
— unknown— unknown
self-pay: ₴0/course
Trial sponsor
Trial · NCT07003542
A Phase 2 and Pharmacodynamic Study of Sitagliptin in Patients With Progressive Grade 4 Gliomas
No UA site listed — international referral required
— unknown— unknown
self-pay: ₴0/course
Trial sponsor
Trial · NCT06419946
Lomustine in Addition to Standard of Care in Patients With MGMT Methylated Glioblastoma
No UA site listed — international referral required
— unknown— unknown
self-pay: ₴0/course
Trial sponsor
Trial · NCT03672721
IA Carboplatin + Radiotherapy in Relapsing GBM
No UA site listed — international referral required
— unknown— unknown
self-pay: ₴0/course
Trial sponsor
Trial · NCT07209241
Different Approaches for CART-EGFR-IL13Ra2 Dosing in Recurrent GBM
No UA site listed — international referral required
— unknown— unknown
self-pay: ₴0/course
Trial sponsor
Trial · NCT05734560
D2C7-IT and 2141-V11 in Newly Diagnosed GBM Patients
No UA site listed — international referral required
— unknown— unknown
self-pay: ₴0/course
Trial sponsor
Trial · NCT06418113
Neoadjuvant Radio-chemotherapy Safety Pilot Study in Patients With Glioblastoma
No UA site listed — international referral required
— unknown— unknown
self-pay: ₴0/course
Trial sponsor
Trial · NCT06047379
Safety and Efficacy of NEO212 in Patients With Astrocytoma IDH-mutant, Glioblastoma IDH-wildtype or Brain Metastasis
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: 2026-05-13.