OpenOnco · Granulosa cell tumor - carboplatin/paclitaxel 1L
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OpenOnco · Treatment Plan
Treatment plan — Adult granulosa cell tumor
PLAN-COVERAGE-GRANULOSA-CELL-001-V1 · v1 · 2026-05-13
Patient
COVERAGE-GRANULOSA-CELL-001 · Algorithm: ALGO-GRANULOSA-CELL-1L
DiagnosisAdult granulosa cell tumor
MOH / ICD-10C56
ICD-O-38620/3; C56

Clinical significance of mutations (ESCAT)

Tumor-board context — the engine does not use these tiers to rank tracks
BiomarkerVariantESCATEvidenceClinical significanceDrugsSources
No clinically actionable variants matched in this profile.

Primary current-line option

Standard plan
★ DEFAULT
Indication
IND-GRANULOSA-CELL-1L-CARBOPLATIN-PACLITAXEL
Regimen
Carboplatin + Paclitaxel (adult granulosa cell tumor, advanced/recurrent)
Drugs + NSZU
  • Carboplatin (DRUG-CARBOPLATIN) AUC 5–6 IV on Day 1 · Every 21 days · IV ⚠ NSZU — not for this indication
  • Paclitaxel (DRUG-PACLITAXEL) 175 mg/m² IV over 3 hours on Day 1 · Every 21 days · IV ⚠ NSZU — not for this indication
Reason
Primary current-line option selected by ALGO-GRANULOSA-CELL-1L at step 2.

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

What NOT to do

Explicit prohibitive rules, each grounded in a regimen / supportive care / contraindication entity
Standard plan (IND-GRANULOSA-CELL-1L-CARBOPLATIN-PACLITAXEL)
  • Do NOT ignore Inhibin B and AMH as tumor markers — primary markers for GCT response/recurrence monitoring
  • Do NOT skip paclitaxel premedication (dexamethasone + diphenhydramine + H2-blocker) — hypersensitivity risk
  • Do NOT ignore paclitaxel neuropathy — cumulative, may be permanent
  • Do NOT ignore endocrine component — estrogen excess in GCT; endometrial surveillance

Timeline

Treatment timeline — derived from regimen + monitoring schedule

Standard plan

Induction · Carboplatin + Paclitaxel (adult granulosa cell tumor, advanced/recurrent)
21-day cycles × 6 cycles (standard adjuvant/advanced); adjust for recurrent disease

MDT brief

Discussion questions (1, 1 blocking)

MDT talk tree (1 steps)

#OwnerTopicAction
1molecular_geneticistBiomarker status BLOCKINGWhat is the status of FOXL2 p.C134W mutation (BIO-FOXL2)? It is required by track(s): IND-GRANULOSA-CELL-1L-CARBOPLATIN-PACLITAXEL. Expected value: FOXL2 C134W mutation — confirms adult GCT diagnosis (near-pathognomonic ~97%); not a therapeutic selection marker.

Skills (recommended) — for consideration (1)

  • Molecular geneticist / molecular oncologist recommended
    Indication references an actionable genomic biomarker — mutation / target / actionability interpretation needed.
    Owns: OQ-BIOMARKER-FOXL2

Data quality

Incomplete for default-track review. Default-track review is incomplete until required biomarker gaps are resolved.
  • Biomarker coverage: 0/1 known (0%), 1 missing, 1 default-track gaps
Missing biomarkerLabelMDT ownerDefault trackRequired byNext action
BIO-FOXL2FOXL2 p.C134W mutationmolecular_geneticistyesIND-GRANULOSA-CELL-1L-CARBOPLATIN-PACLITAXELVerify result, method, specimen, and report date before sign-off. Expected/constraint: FOXL2 C134W mutation — confirms adult GCT diagnosis (near-pathognomonic ~97%); not a therapeutic selection marker
Technical MDT skill metadata (1/16 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)
NCT05872204Abemaciclib and Letrozole in Patients With Estrogen Receptor-positive Rare Ovarian CancerPHASE2RECRUITINGUniversitaire Ziekenhuizen KU LeuvenSurrogate endpoint only

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
Carboplatin + Paclitaxel (adult granulosa cell tumor, advanced/recurrent) (REG-CARBOPLATIN-PACLITAXEL-GCT)
✓ registered✓ covered₴-? — verify pathwayNSZU formulary
Trial · NCT05872204
Abemaciclib and Letrozole in Patients With Estrogen Receptor-positive Rare Ovarian Cancer
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.