OpenOnco v0.1.2 · 2026-04-30
OpenOnco · DIS-ET · BIO-CALR (ESCAT IA)
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OpenOnco · Treatment Plan
Treatment plan — DIS-ET
PLAN-BMA-CALR_ET-V1 · v1 · 2026-05-04
Patient
BMA-CALR_ET · Algorithm: ALGO-ET-1L

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-CALRNot in KB — ask clinician to verify

Treatment options (2 tracks)

Standard plan
★ DEFAULT
Indication
IND-ET-1L-ASA
Regimen
Hydroxyurea (PV / ET high-risk 1L cytoreduction) + baseline phlebotomy/ASA
Drugs + NSZU
  • Hydroxyurea (DRUG-HYDROXYUREA) Start 500-1500 mg/day PO (15-25 mg/kg/day); titrate to target · continuous PO daily; titrate by CBC q2-4wk initially, then q1-3 mo once stable · PO ✓ NSZU covered
  • Aspirin (DRUG-ASPIRIN) 81-100 mg PO daily (low-dose aspirin) · continuous · PO ⚠ Out-of-pocket
Reason
Engine default per algorithm ALGO-ET-1L: {'step': 3, 'outcome': False, 'branch': {'result': 'IND-ET-1L-ASA'}, 'fired_red_flags': [], 'winner_red_flag': None}
Aggressive plan
Indication
IND-ET-1L-HU
Regimen
Hydroxyurea (PV / ET high-risk 1L cytoreduction) + baseline phlebotomy/ASA
Drugs + NSZU
  • Hydroxyurea (DRUG-HYDROXYUREA) Start 500-1500 mg/day PO (15-25 mg/kg/day); titrate to target · continuous PO daily; titrate by CBC q2-4wk initially, then q1-3 mo once stable · PO ✓ NSZU covered
  • Aspirin (DRUG-ASPIRIN) 81-100 mg PO daily (low-dose aspirin) · continuous · PO ⚠ Out-of-pocket
Reason
Alternative track presented for HCP consideration

Pre-treatment investigations

Investigations before treatment start · critical / standard / desired · merged across tracks
IDNamePriorityCategoryWhere to orderNeeded for
TEST-BCR-ABL-JAK2BCR-ABL + JAK2 + CALR + MPLCriticalgenomicCSD Lab ✓ (code TBC)all tracks
TEST-BM-ASPIRATEBone Marrow AspirateCriticalhistologyall tracks
TEST-BM-TREPHINEBone Marrow TrephineCriticalhistologyall tracks
TEST-CBCComplete Blood Count with DifferentialCriticallaball tracks
TEST-CMPComprehensive Metabolic PanelCriticallaball tracks
TEST-COAG-PANELCoagulation PanelCriticallaball tracks
TEST-FLOW-CYTOMETRYFlow CytometryCriticalhistologyCSD Lab ✓ (code TBC)all tracks
TEST-HBV-SEROLOGYHepatitis B Serology Panel (HBsAg, anti-HBc total, anti-HBs)Criticallaball tracks
TEST-KARYOTYPEKaryotypeCriticalgenomicCSD Lab ✓ (code TBC)all tracks
TEST-LDHLactate DehydrogenaseCriticallaball tracks
TEST-LFTLiver Function Tests (ALT, AST, bilirubin, ALP, GGT, albumin)Criticallaball tracks
TEST-NGS-MYELOID-PANELMyeloid NGS PanelCriticalgenomicCSD Lab ✓ (code TBC)all tracks
TEST-PERIPHERAL-SMEARPeripheral Blood SmearCriticallabCSD Lab ✓ (code TBC)all tracks
TEST-PREGNANCYBeta-HCGCriticallabaggressive
TEST-ECHOEchocardiographyStandardimagingdesired (aggressive)
TEST-IRON-PANELIron PanelStandardlaball tracks
TEST-RETICULOCYTEReticulocyte CountStandardlaball tracks
TEST-D-DIMERD-DimerDesiredlaball tracks

Red flags — PRO / CONTRA aggressive

PRO-AGGRESSIVE

Triggers that push toward the aggressive track
  • ET transformation to post-ET myelofibrosis (~5-10% over 15 years) or to AML / MDS (rare ~1-5%): rising LDH, new splenomegaly, leukoerythroblastic smear, increasing reticulin fibrosis on trephine, blast appearance — re-stage, switch to MF or AML algorithmRF-ET-TRANSFORMATION-PROGRESSION
  • PV or ET patient elderly or frail (age ≥80, ECOG ≥3, multiple comorbidities, life expectancy <5 years) — gentler cytoreduction (lower HU dose), expanded transfusion + monitoring strategyRF-PV-ET-FRAILTY-AGE
  • PV or ET high-risk for thrombosis: age >60 OR prior arterial / venous thrombosis OR (ET only) JAK2 V617F + CV risk factors (IPSET-thrombosis high) — triggers cytoreduction (HU 1L) in addition to baseline phlebotomy + ASARF-PV-ET-HIGH-THROMBOSIS-RISK
  • PV or ET patient with organ dysfunction limiting cytoreductive choice: severe renal impairment (CrCl <30 — limits HU), severe hepatic dysfunction (limits ruxolitinib), or severe cardiac dysfunction (limits anagrelide)RF-PV-ET-ORGAN-DYSFUNCTION
  • PV or ET patient pregnant or planning pregnancy — HU and anagrelide contraindicated; switch to interferon-α (PEG-IFN-α2a or ropeginterferon)RF-PV-ET-PREGNANCY-OR-PLANNING

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-ET-1L-ASA)
  • Do not skip JAK2 / CALR / MPL testing — driver-mutation status determines subtype + IPSET-thrombosis risk.
  • Do not prescribe ASA in extreme thrombocytosis (plt >1500K) without ruling out acquired vWD — check ristocetin cofactor activity.
  • Do not skip prefibrotic-PMF differential on trephine — same presentation, worse prognosis.
  • Do not prescribe anagrelide 1L — PT-1 trial showed lower cardiovascular profile + HU more preferable.
  • Do not use full-dose ASA — low-dose is standard.
Aggressive plan (IND-ET-1L-HU)
  • Do not prescribe HU during pregnancy / pregnancy plans — switch to IFN-α.
  • Do not skip monthly CBC for the first 3 months — myelosuppression-titrating.
  • Do not use anagrelide 1L — PT-1 trial showed HU advantage on arterial thrombosis and MF progression.
  • Do not prescribe in cutaneous ulceration history — risk of recurrence.
  • Do not combine with peg-IFN without a clear protocol.

MDT brief

Skills (recommended) — for consideration (2)

  • Clinical pharmacist recommended
    Chemoimmunotherapy regimen — drug-drug interactions, dose adjustments, premedication.
    skill: clinical_pharmacistv0.1.0reviewed 2026-04-25STUBsign-offs: 0lead: TBD
  • Social worker / case manager recommended
    Plan includes drugs without NSZU reimbursement — patient access pathway must be assessed.
    skill: social_worker_case_managerv0.1.0reviewed 2026-04-25STUBsign-offs: 0lead: TBD

Open questions (1, 0 blocking)

  • OQ-LDH-CURRENT
    What is the current LDH? Marker of tumor burden and transformation.
    LDH is part of the prognostic indices of indolent lymphomas.
    → hematologist

Data quality

  • Unevaluated RedFlags: RF-ET-TRANSFORMATION-PROGRESSION, RF-PV-ET-FRAILTY-AGE, RF-PV-ET-HIGH-THROMBOSIS-RISK, RF-PV-ET-INFECTION-SCREENING, RF-PV-ET-ORGAN-DYSFUNCTION, RF-PV-ET-PREGNANCY-OR-PLANNING

Skill catalog (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: 2026-05-04.
NCTTitlePhaseStatusSponsorUAEligibility (excerpt)
NCT06770842Ropeginterferon Alfa 2b Plus Ruxolitinib for MyelofibrosisPHASE2RECRUITINGThe University of Hong Kong
NCT05123365An Optimal Dose Finding Study of N-Acetylcysteine in Patients With Myeloproliferative NeoplasmsPHASE1 / PHASE2RECRUITINGUniversity of California, Irvine
NCT06218628Pacritinib w/ Talazoparib in Pts w/ Myeloproliferative Neoplasms Unresponsive to JAK2 InhibitionPHASE1RECRUITINGFox Chase Cancer Center
NCT07362225MPN PROGRESSion Registry: Observational Study Tracking Symptoms, Treatments, and Disease Progression in People With Myeloproliferative Neoplasms (MPNs)N/ARECRUITINGMPN Research Foundation
NCT02897297Myeloproliferative Neoplastic Diseases Observatory From BrestN/ARECRUITINGUniversity Hospital, Brest
NCT04942080Interest of CALR Allele Burden in Diagnosis and Follow-up of Patients With CALR Mutated Myeloproliferative Syndromes (CALRSUIVI)NARECRUITINGUniversity Hospital, Angers
NCT06351631A Study to Evaluate Safety and Efficacy of Bomedemstat (MK-3543-017)PHASE3RECRUITINGMerck Sharp & Dohme LLC
NCT06976918Registry Platform Myelofibrosis and AnemiaN/ARECRUITINGiOMEDICO AG
NCT05882773Asian Myeloproliferative Neoplasm (MPN) RegistryN/ARECRUITINGThe University of Hong Kong
NCT06456346Bomedemstat vs Hydroxyurea for Essential Thrombocythemia (MK-3543-007)PHASE3RECRUITINGMerck Sharp & Dohme LLC

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
Hydroxyurea (PV / ET high-risk 1L cytoreduction) + baseline phlebotomy/ASA (REG-HU-PV-ET)
1/2 component drug(s) not on NSZU formulary
✓ registered✗ out-of-pocket₴-? — verify pathwaynot recorded
Aggressive plan
Hydroxyurea (PV / ET high-risk 1L cytoreduction) + baseline phlebotomy/ASA (REG-HU-PV-ET)
1/2 component drug(s) not on NSZU formulary
✓ registered✗ out-of-pocket₴-? — verify pathwaynot recorded
Trial · NCT06770842
Ropeginterferon Alfa 2b Plus Ruxolitinib for Myelofibrosis
No UA site listed — international referral required
— unknown— unknown
self-pay: ₴0/course
Trial sponsor
Trial · NCT05123365
An Optimal Dose Finding Study of N-Acetylcysteine in Patients With Myeloproliferative Neoplasms
No UA site listed — international referral required
— unknown— unknown
self-pay: ₴0/course
Trial sponsor
Trial · NCT06218628
Pacritinib w/ Talazoparib in Pts w/ Myeloproliferative Neoplasms Unresponsive to JAK2 Inhibition
No UA site listed — international referral required
— unknown— unknown
self-pay: ₴0/course
Trial sponsor
Trial · NCT07362225
MPN PROGRESSion Registry: Observational Study Tracking Symptoms, Treatments, and Disease Progression in People With Myeloproliferative Neoplasms (MPNs)
No UA site listed — international referral required
— unknown— unknown
self-pay: ₴0/course
Trial sponsor
Trial · NCT02897297
Myeloproliferative Neoplastic Diseases Observatory From Brest
No UA site listed — international referral required
— unknown— unknown
self-pay: ₴0/course
Trial sponsor
Trial · NCT04942080
Interest of CALR Allele Burden in Diagnosis and Follow-up of Patients With CALR Mutated Myeloproliferative Syndromes (CALRSUIVI)
No UA site listed — international referral required
— unknown— unknown
self-pay: ₴0/course
Trial sponsor
Trial · NCT06351631
A Study to Evaluate Safety and Efficacy of Bomedemstat (MK-3543-017)
No UA site listed — international referral required
— unknown— unknown
self-pay: ₴0/course
Trial sponsor
Trial · NCT06976918
Registry Platform Myelofibrosis and Anemia
No UA site listed — international referral required
— unknown— unknown
self-pay: ₴0/course
Trial sponsor
Trial · NCT05882773
Asian Myeloproliferative Neoplasm (MPN) Registry
No UA site listed — international referral required
— unknown— unknown
self-pay: ₴0/course
Trial sponsor
Trial · NCT06456346
Bomedemstat vs Hydroxyurea for Essential Thrombocythemia (MK-3543-007)
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: 2026-05-04.