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heme.acute-leukemia.core.v1PRODUCTION
heme.acute-leukemia.core.v1
Acute Leukemia (AML / ALL / APL)
oncologyacuteadult
Hard-required inputs
0 / 5
Care setting:
Encounter flow
12/12 authoredCanonical 12-phase frame with authored status for this dossier.
Current phase
Frame
Suspect acute leukemia from blasts on smear; APL recognition is the time-critical priority
Inputs
2
Actions
0
Advance rule
Set
Advance when
Acute leukemia suspected
Patient inputs (7)
Fit vs unfit determines 7+3 vs venetoclax+aza (VIALE-A)
WBC + blast %; hyperleukocytosis triggers leukapheresis decision
Auer rods → AML; faggot cells → APL; lymphoblasts → ALL
DIC concern in APL — fibrinogen + D-dimer + PT
Uric acid + K + Phos + Ca for TLS risk
Lineage assignment AML/ALL + immunophenotype
t(15;17) APL → STAT ATRA; t(9;22) Ph+ ALL → TKI; risk strat for AML
* = hard-required. Engine cannot meaningfully run until these are filled.
Severity triggers (8)
8 need judgement
- informationallife_threateningAPL DIC pattern (NCCN 2024 APL)Promyelocytes + DIC (low fibrinogen + high D-dimer + bleeding) (NCCN 2024 APL)Trigger could not be auto-evaluated — needs clinician judgement.
- informationallife_threateningleukostasis (NCCN 2024 AML)WBC >100k + CNS / pulmonary / cardiac symptoms (NCCN 2024 AML)Trigger could not be auto-evaluated — needs clinician judgement.
- informationallife_threateningspinal cord compression (NCCN 2024)Back pain + neurologic deficit in leukemia patient (NCCN 2024)Trigger could not be auto-evaluated — needs clinician judgement.
- informationallife_threateningDIC severe (NCCN 2024 APL)Fibrinogen <150 + bleeding + APL/sepsis context (NCCN 2024 APL)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalsevereTLS high risk (Cairo-Bishop; NCCN 2024)WBC >50k OR uric acid >8 OR LDH >2x ULN OR Burkitt-like (Cairo-Bishop 2004; NCCN 2024)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalseverefebrile neutropenia (IDSA 2010; NCCN 2024)Fever ≥38.3 OR ≥38.0 sustained + ANC <500 (IDSA 2010)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalseveredifferentiation syndrome (NCCN 2024 APL)On ATRA/ATO + dyspnea + fever + edema + hypotension (NCCN 2024 APL)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalsevereCNS leukemia (NCCN 2024 ALL)CNS symptoms or positive CSF cytology (NCCN 2024 ALL)Trigger could not be auto-evaluated — needs clinician judgement.
Workflow calculators
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Recommended regimen
Subtype-driven induction (ELN 2022 AML / NCCN ALL / NCCN APL)axis: leukemia_subtype_inductionstep apl - APL t(15;17) — STAT ATRA + arsenic at suspicion
Selected step "APL t(15;17) — STAT ATRA + arsenic at suspicion" — Suspicion of APL (DIC + faggot cells + promyelocytes + low/intermediate WBC)
- all_trans_retinoic_acidfirst linedifferentiating_agent45 mg/m²/day PO divided BID • PO • BIDtriggers: apl_suspectedLo-Coco NEJM 2013; do NOT wait for confirmation; differentiation syndrome prophylaxis with steroidrxcui 10753
- arsenic_trioxidefirst linedemethylating_agent0.15 mg/kg/day IV • IV • daily until remission then consolidationtriggers: apl_confirmed_low_intermediate_riskLo-Coco NEJM 2013 — chemo-free for low/intermediate; QTc monitoringrxcui 18330
- prednisoneadd oncorticosteroid0.5 mg/kg PO daily • PO • dailytriggers: differentiation_syndrome_prophylaxisPrevent dyspnea/fever/edema syndromerxcui 8640
- idarubicinadd onanthracycline12 mg/m²/d × 4 days • IV • days 2,4,6,8triggers: high_risk_apl, WBC>10kHigh-risk APL adds anthracyclinerxcui 5650
ed playbook — drug actions (6)
- 1. all-trans retinoic acid (ATRA)45 mg/m²/day PO BID • PO • BIDtrigger: APL suspected (DIC + faggot cells + promyelocytes)Lo-Coco NEJM 2013 — do not wait for confirmation
- 2. rasburicase0.2 mg/kg IV • IV • single dosetrigger: High TLS risk (WBC >50k or uric acid >8)TLS prophylaxis/rescue; check G6PD if applicable
- 3. allopurinol300 mg PO daily • PO • dailytrigger: Low/intermediate TLS riskTLS prophylaxis
- 4. IV fluids hyperhydration3 L/m²/day NS or LR • IV • continuoustrigger: TLS prophylaxisMaintain UOP >100 mL/m²/h
- 5. cefepime or pip-tazoCefepime 2 g IV q8h OR pip-tazo 4.5 g IV q6h • IV • q6-8htrigger: Febrile neutropenia (fever + ANC <500)IDSA — treat as sepsis
- 6. platelet transfusion1 unit apheresis • IV • as neededtrigger: Plt <10k OR <50k + bleeding/procedure OR DICBleeding prevention
Auto-drafted A&P note
edSubjective
- Possible entry pathways: Leukocytosis with circulating blasts on smear; Pancytopenia + blasts; Bleeding / DIC (concern for APL).
Objective
- No vitals, labs, or imaging entered for this encounter.
Assessment
**Acute Leukemia (AML / ALL / APL)** (heme.acute-leukemia.core.v1). Phenotype framing: AML / ALL / APL t(15;17) / mixed-phenotype / blast crisis CML / lymphoma leukemic phase Scope: Suspect acute leukemia from blasts on smear; APL recognition is the time-critical priority No severity triggers fired against current inputs.
Plan
Regimen axis: **Subtype-driven induction (ELN 2022 AML / NCCN ALL / NCCN APL)** — step "APL t(15;17) — STAT ATRA + arsenic at suspicion". 1. all_trans_retinoic_acid 45 mg/m²/day PO divided BID PO BID (differentiating_agent, first line) — Lo-Coco NEJM 2013; do NOT wait for confirmation; differentiation syndrome prophylaxis with steroid 2. arsenic_trioxide 0.15 mg/kg/day IV IV daily until remission then consolidation (demethylating_agent, first line) — Lo-Coco NEJM 2013 — chemo-free for low/intermediate; QTc monitoring 3. prednisone 0.5 mg/kg PO daily PO daily (corticosteroid, add on) — Prevent dyspnea/fever/edema syndrome 4. idarubicin 12 mg/m²/d × 4 days IV days 2,4,6,8 (anthracycline, add on) — High-risk APL adds anthracycline Setting playbook (ed) — Recognize leukemia, identify life-threatening complications (DIC/leukostasis/TLS/sepsis), expedite to heme/onc 5. all-trans retinoic acid (ATRA) 45 mg/m²/day PO BID PO BID — APL suspected (DIC + faggot cells + promyelocytes) (Lo-Coco NEJM 2013 — do not wait for confirmation) 6. rasburicase 0.2 mg/kg IV IV single dose — High TLS risk (WBC >50k or uric acid >8) (TLS prophylaxis/rescue; check G6PD if applicable) 7. allopurinol 300 mg PO daily PO daily — Low/intermediate TLS risk (TLS prophylaxis) 8. IV fluids hyperhydration 3 L/m²/day NS or LR IV continuous — TLS prophylaxis (Maintain UOP >100 mL/m²/h) 9. cefepime or pip-tazo Cefepime 2 g IV q8h OR pip-tazo 4.5 g IV q6h IV q6-8h — Febrile neutropenia (fever + ANC <500) (IDSA — treat as sepsis) 10. platelet transfusion 1 unit apheresis IV as needed — Plt <10k OR <50k + bleeding/procedure OR DIC (Bleeding prevention) Non-pharmacologic actions: - Leukapheresis if leukostasis (WBC >100k + symptoms) - STAT heme/onc consult - Reverse isolation if neutropenic - IV access (large-bore × 2; avoid central if DIC) AVOID / contraindication checks: - ATRA differentiation syndrome prophylaxis with prednisone (NCCN 2024 APL) - Arsenic QTc monitor q1w (NCCN 2024 APL; Lo Coco NEJM 2013) - Venetoclax TLS ramp up and prophylaxis (NCCN 2024 AML; VIALE A DiNardo NEJM 2020) - Rasburicase G6PD screen (NCCN 2024 AML/ALL) - Anthracycline cumulative dose limit (NCCN 2024 AML) - Cytarabine conjunctivitis prophylaxis with steroid eye drops (NCCN 2024 AML)
Monitoring
Regimen monitoring: - Daily CBC + differential (NCCN 2024 AML/ALL) - Daily coags + fibrinogen if APL (NCCN 2024 APL) - Daily TLS labs (K, Phos, Ca, uric acid, LDH, Cr) (NCCN 2024 AML/ALL) - QTc q1w on arsenic (NCCN 2024 APL; Lo-Coco NEJM 2013) - LFTs q1w (NCCN 2024 AML) - Echo before each anthracycline cycle (NCCN 2024 AML) - Surveillance cultures + chest CT for pulmonary infiltrates (NCCN 2024 AML/ALL) Setting (ed) monitoring: - Continuous cardiac telemetry (NCCN 2024 AML/ALL) - Q4-6h TLS labs (NCCN 2024) - Hourly UOP (NCCN 2024) - Coag q4-6h if DIC (NCCN 2024 APL) Follow-up plan: Consolidation + maintenance per protocol; MRD assessment; survivorship + late-effect screening - Close-out criterion: Long-term plan documented Monitoring phase: Daily CBC + coag (APL DIC) + TLS labs; differentiation syndrome monitoring on ATRA; mucositis + neutropenic fever; QTc on arsenic
Disposition
Current setting: ed — Recognize leukemia, identify life-threatening complications (DIC/leukostasis/TLS/sepsis), expedite to heme/onc Disposition criteria: - Admit heme/onc inpatient for induction (NCCN 2024 AML/ALL) - Admit ICU if leukostasis, DIC, septic shock (NCCN 2024) Escalation triggers (move to higher acuity): - Leukostasis with CNS/pulm symptoms → ICU + leukapheresis (NCCN 2024 AML) - Severe DIC with bleeding → ICU + cryoprecipitate + FFP (NCCN 2024 APL) - Septic shock → ICU + pressors (NCCN 2024) - Spinal cord compression → STAT MRI + radiation/dex (NCCN 2024)
Earlier-Return Triggers
Return-precaution thresholds (watch for): - [LIFE_THREATENING] Promyelocytes + DIC (low fibrinogen + high D-dimer + bleeding) (NCCN 2024 APL) - [LIFE_THREATENING] WBC >100k + CNS / pulmonary / cardiac symptoms (NCCN 2024 AML) - [LIFE_THREATENING] Back pain + neurologic deficit in leukemia patient (NCCN 2024)
Citations
- ELN 2022 AML Recommendations (Döhner et al, Blood 2022) + 2024 ELN less-intensive-therapy risk refinement; APL0406 ATRA+arsenic (Lo-Coco NEJM 2013, final JCO 2016); VIALE-A azacitidine+venetoclax (DiNardo NEJM 2020); ELIANA tisagenlecleucel CAR-T (Maude NEJM 2018); NCCN AML/ALL/APL [PMID:35797463](https://pubmed.ncbi.nlm.nih.gov/35797463/) - Cited evidence (PMID 32786187) [PMID:32786187](https://pubmed.ncbi.nlm.nih.gov/32786187/) - Cited evidence (PMID 23841729) [PMID:23841729](https://pubmed.ncbi.nlm.nih.gov/23841729/) - Cited evidence (PMID 27400939) [PMID:27400939](https://pubmed.ncbi.nlm.nih.gov/27400939/) - Cited evidence (PMID 29385370) [PMID:29385370](https://pubmed.ncbi.nlm.nih.gov/29385370/) Last reconciled with current guidelines: 2026-05-22.
References
- ELN 2022 AML Recommendations (Döhner et al, Blood 2022) + 2024 ELN less-intensive-therapy risk refinement; APL0406 ATRA+arsenic (Lo-Coco NEJM 2013, final JCO 2016); VIALE-A azacitidine+venetoclax (DiNardo NEJM 2020); ELIANA tisagenlecleucel CAR-T (Maude NEJM 2018); NCCN AML/ALL/APL — PMID:35797463
- Cited evidence (PMID 32786187) — PMID:32786187
- Cited evidence (PMID 23841729) — PMID:23841729
- Cited evidence (PMID 27400939) — PMID:27400939
- Cited evidence (PMID 29385370) — PMID:29385370