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OpenOnco · DIS-CHL · BIO-CD30-IHC (ESCAT IA)
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Treatment plan — DIS-CHL
PLAN-BMA-CD30_CHL-V1 · v1 · 2026-05-04
Patient
BMA-CD30_CHL · Algorithm: ALGO-CHL-1L

Clinical significance of mutations (ESCAT)

Tumor-board context — the engine does not use these tiers to rank tracks
BiomarkerVariantESCATEvidenceClinical significanceDrugsSources
BIO-CD30-IHCCD30 expression on Reed-Sternberg / Hodgkin cells (~100% positive by IHC — defining feature of classical Hodgkin lymphoma)IA
  • SRC-NCCN-BCELL-2025
  • SRC-ESMO-HODGKIN-2024
Evidence cited from clinical guidelines; per-source evidence levels not yet structured. See Phase-2-of-CIViC-pivot for re-cite roadmap.
CD30 is universally expressed on Reed-Sternberg cells in classical Hodgkin lymphoma and is the target of brentuximab vedotin (BV), an anti-CD30 antibody-drug conjugate (auristatin payload). 1L advanced- stage cHL: A+AVD (BV + doxorubicin/vinblastine/dacarbazine) is preferred over ABVD per ECHELON-1 (Ansell NEJM 2022 — 6y OS 93.9% vs 89.4%, HR 0.59) per SRC-NCCN-BCELL-2025, SRC-ESMO-HODGKIN-2024. Pediatric AHOD1331 supported BV + AVE-PC for high-risk pediatric. R/R cHL: BV monotherapy and BV + nivolumab are standard pre-/post- HCT options. BV consolidation post-autoHCT for high-risk R/R cHL (AETHERA Younes Lancet 2015 — improves PFS) per SRC-NCCN-BCELL-2025.A+AVD (brentuximab vedotin + AVD) — 1L stage III/IV cHL per SRC-NCCN-BCELL-2025, SRC-ESMO-HODGKIN-2024
brentuximab vedotin + nivolumab — R/R cHL pre-/post-autoHCT per SRC-NCCN-BCELL-2025
brentuximab vedotin consolidation post-autoHCT — high-risk R/R cHL per SRC-NCCN-BCELL-2025
  • SRC-NCCN-BCELL-2025
  • SRC-ESMO-HODGKIN-2024

Treatment options (2 tracks)

Standard plan
★ DEFAULT
Indication
IND-CHL-1L-ABVD
Regimen
ABVD (Adriamycin + Bleomycin + Vinblastine + Dacarbazine), 2-6 cycles
Drugs + NSZU
  • Doxorubicin (DRUG-DOXORUBICIN) 25 mg/m² · IV days 1+15 of 28-day cycle · IV ✓ NSZU covered
  • Bleomycin (DRUG-BLEOMYCIN) 10 units/m² · IV days 1+15 of 28-day cycle · IV ✓ NSZU covered
  • Vinblastine (DRUG-VINBLASTINE) 6 mg/m² · IV days 1+15 of 28-day cycle · IV ✓ NSZU covered
  • Dacarbazine (DRUG-DACARBAZINE) 375 mg/m² · IV days 1+15 of 28-day cycle · IV ✓ NSZU covered
Supportive care
SUP-ANTIEMETIC-PREMED
Hard contraindications
CI-LVEF-LOW-FOR-ANTHRACYCLINE
Reason
Engine default per algorithm ALGO-CHL-1L: {'step': 1, 'outcome': False, 'branch': {'result': 'IND-CHL-1L-ABVD'}, 'fired_red_flags': [], 'winner_red_flag': None}
Aggressive plan
Indication
IND-CHL-1L-A-AVD
Regimen
A+AVD (Brentuximab vedotin + Adriamycin + Vinblastine + Dacarbazine), 6 cycles
Drugs + NSZU
  • Brentuximab vedotin (DRUG-BRENTUXIMAB-VEDOTIN) 1.2 mg/kg · IV days 1+15 of 28-day cycle × 6 · IV ✓ NSZU covered
  • Doxorubicin (DRUG-DOXORUBICIN) 25 mg/m² · IV days 1+15 of 28-day cycle · IV ✓ NSZU covered
  • Vinblastine (DRUG-VINBLASTINE) 6 mg/m² · IV days 1+15 of 28-day cycle · IV ✓ NSZU covered
  • Dacarbazine (DRUG-DACARBAZINE) 375 mg/m² · IV days 1+15 of 28-day cycle · IV ✓ NSZU covered
Supportive care
SUP-ANTIEMETIC-PREMED, SUP-GCSF-NEUTROPENIA
Hard contraindications
CI-LVEF-LOW-FOR-ANTHRACYCLINE, CI-BORTEZOMIB-SEVERE-NEUROPATHY, CI-HBV-NO-PROPHYLAXIS
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-CBCComplete Blood Count with DifferentialCriticallab—all tracks
TEST-CMPComprehensive Metabolic PanelCriticallab—all tracks
TEST-HBV-SEROLOGYHepatitis B Serology Panel (HBsAg, anti-HBc total, anti-HBs)Criticallab—all tracks
TEST-HIV-SEROLOGYHIV Antibody/AntigenCriticallab—all tracks
TEST-LDHLactate DehydrogenaseCriticallab—all tracks
TEST-LFTLiver Function Tests (ALT, AST, bilirubin, ALP, GGT, albumin)Criticallab—all tracks
TEST-LN-EXCISIONAL-BIOPSYExcisional LN BiopsyCriticalhistology—all tracks
TEST-PREGNANCYBeta-HCGCriticallab—all tracks
TEST-ECHOEchocardiographyStandardimaging—all tracks
TEST-PET-CTFDG PET/CT (whole body)Standardimaging—all tracks

Red flags — PRO / CONTRA aggressive

PRO-AGGRESSIVE

Triggers that push toward the aggressive track
  • Classical Hodgkin lymphoma stage III-IV (advanced) — selects A+AVD (ECHELON-1) over ABVD if brentuximab accessibleRF-CHL-ADVANCED-STAGE

CONTRA-AGGRESSIVE

Hard contraindications to escalation
  • Pre-treatment LVEF <50% is an absolute contraindication to anthracycline-containing regimens (R-CHOP, Pola-R-CHP, ABVD, BV-AVD, etc.). Cardiotoxicity from doxorubicin is dose-cumulative and often irreversible; starting with already-impaired function risks acute decompensation.CI-LVEF-LOW-FOR-ANTHRACYCLINE
  • Severe pre-existing peripheral neuropathy is an absolute contraindication to bortezomib — therapy will likely worsen the neuropathy to a disabling and often permanent extent.CI-BORTEZOMIB-SEVERE-NEUROPATHY
  • Active or latent HBV without antiviral prophylaxis is an absolute contraindication to starting B-cell-depleting / immunomodulatory monoclonal antibody therapy (anti-CD20, anti-CD30 ADC, anti-CD38). Severe HBV reactivation hepatitis risk including fulminant hepatic failure.CI-HBV-NO-PROPHYLAXIS

What NOT to do

Explicit prohibitive rules, each grounded in a regimen / supportive care / contraindication entity
Standard plan (IND-CHL-1L-ABVD)
  • Do NOT combine with brentuximab vedotin — ABSOLUTE pulmonary toxicity contraindication.
  • Do NOT use G-CSF on ABVD — increases pulmonary toxicity of bleomycin.
  • Do NOT continue bleomycin with DLCO drop ≥25% — switch to AVD (drop bleo).
  • Do NOT skip baseline LVEF + DLCO + fertility preservation discussion.
  • Do NOT use high-flow O2 during anesthesia after bleomycin (lifetime risk).
  • Do NOT start without HBV screening + entecavir prophylaxis if HBsAg+ — reactivation on steroid pulse is real (also actionable if anti-HBc+ — monitor HBV-DNA q-cycle).
  • Do NOT interrupt ART in HIV+ patients — HIV-HL outcomes approach HIV-negative cHL with concurrent ART; avoid ritonavir-boosted PIs (vincristine interaction); PJP prophylaxis throughout.
Aggressive plan (IND-CHL-1L-A-AVD)
  • Do NOT combine brentuximab with bleomycin — ABSOLUTE; lethality risk.
  • Do NOT skip G-CSF support — neutropenia with brentuximab + anti-mitotic is higher.
  • Do NOT ignore pre-existing peripheral neuropathy — Grade ≥2 = absolute CI.
  • Do NOT prescribe without a verified funding pathway — brentuximab is not NSZU-reimbursed.
  • Do NOT start brentuximab without HBV screening + entecavir prophylaxis if HBsAg+ or anti-HBc+ — anti-CD30 ADC has documented HBV reactivation risk; continue ≥12 mo after last BV dose.
  • Do NOT interrupt ART in HIV+ — A+AVD is acceptable with ART; integrase backbone preferred (vincristine-PI interaction); PJP prophylaxis throughout.

Monitoring schedule

Monitoring schedule by treatment phase

Standard plan · MON-R-CHOP-REGIMEN

PhaseWindowTestsCheckpoints
baselineWithin 2 weeks before cycle 1TEST-CBC, TEST-CMP, TEST-LFT, TEST-LDH, TEST-B2-MICROGLOBULIN, TEST-HBV-SEROLOGY, TEST-HCV-ANTIBODY, TEST-HIV-SEROLOGY, TEST-PET-CT, TEST-LN-EXCISIONAL-BIOPSY, TEST-FLOW-CYTOMETRY, TEST-CD20-IHC, TEST-ECHO, TEST-PREGNANCY, TEST-BM-ASPIRATE, TEST-BM-TREPHINE
  • Confirm CD20+ DLBCL histology; rule out double-hit (FISH for MYC/BCL2/BCL6)
  • Confirm HBV status + entecavir prophylaxis plan if HBsAg+ or anti-HBc+
  • Baseline LVEF ≥50% before doxorubicin
  • IPI calculation documented (age, ECOG, LDH, stage, extranodal sites)
  • CNS-IPI calculation if anatomic risk sites or composite score concerning
  • Fertility preservation discussion (sperm banking / oocyte cryo) for childbearing-age
on_treatmentDay 1 of every 21-day cycleTEST-CBC, TEST-CMP, TEST-LFT
  • ANC ≥1500 + platelets ≥100K before each cycle (delay or G-CSF if not)
  • Neuropathy grade documented (CTCAE) — vincristine modification if ≥2
  • LVEF re-check after cumulative doxorubicin ~300 mg/m²
interim_response_assessmentAfter cycles 2-4 (interim PET-CT)TEST-PET-CT, TEST-LDH
  • Lugano response criteria + Deauville score
  • If Deauville 4-5 with mass progression → consider salvage or trial
end_of_treatmentAfter cycle 6 (within 6-8 weeks)TEST-PET-CT, TEST-CBC, TEST-CMP, TEST-LDH
  • Confirm CR vs PR vs SD vs PD by Lugano/Deauville
  • Begin survivorship plan: cardiac surveillance schedule, vaccination catch-up, second-cancer screening
follow_up_shortEvery 3 months × 2 years post-treatmentTEST-CBC, TEST-CMP, TEST-LFT, TEST-LDH
  • Surveillance for relapse (~40% relapse risk by 2 years overall)
  • HBV reactivation monitoring continues for 12 months post anti-CD20
follow_up_longEvery 6 months years 3-5, then annuallyTEST-CBC, TEST-LFT, TEST-ECHO
  • Late cardiomyopathy screening (LVEF) annually if cumulative dox >300
  • Annual second-malignancy screening (skin, breast, etc. age-appropriate)

Timeline

Treatment timeline — derived from regimen + monitoring schedule

Standard plan

Baseline
Within 2 weeks before cycle 1
Induction · ABVD (Adriamycin + Bleomycin +
28-day cycles × 2-4 (early-stage + ISRT) OR 6 (advanced); response-adapted per interim PET-CT Deauville
Response assessment
After cycles 2-4 (interim PET-CT)
Follow-up
Every 3 months × 2 years post-treatment

Aggressive plan

Baseline
Within 2 weeks before cycle 1
Induction · A+AVD (Brentuximab vedotin + A
28-day cycles × 6
Response assessment
After cycles 2-4 (interim PET-CT)
Follow-up
Every 3 months × 2 years post-treatment

MDT brief

Skills (required) — mandatory virtual specialists (1)

  • Hematologist / oncohematologist required
    Lymphoma diagnosis — leading specialty for treatment management.
    Owns: OQ-LDH-CURRENT
    skill: hematologistv0.1.0reviewed 2026-04-25STUBsign-offs: 0lead: TBD

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
  • Pathologist (general) recommended
    Confirm lymphoma histology + assess transformation risk (DLBCL/Richter).
    Owns: OQ-CD20-CONFIRMATION
    skill: pathologistv0.1.0reviewed 2026-04-25STUBsign-offs: 0lead: TBD

Open questions (3, 1 blocking)

  • BLOCKING OQ-CD20-CONFIRMATION
    Is CD20+ status confirmed by histology (IHC)? Without CD20+, rituximab/obinutuzumab are not indicated.
    Anti-CD20 therapy is the backbone of most lines of treatment; absence of CD20 expression fully changes the regimen.
    → pathologist
  • OQ-STAGING-COMPLETE
    Has complete staging been done (Lugano + PET/CT or CT)?
    Prognosis and track selection depend on stage and tumor burden.
    → radiologist
  • 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

  • Missing critical: cd20_ihc_status, lugano_stage
  • Missing recommended: ldh_ratio_to_uln, fib4_index, pet_ct_date
  • Unevaluated RedFlags: RF-CHL-ADVANCED-STAGE, RF-CHL-FRAILTY-AGE, RF-CHL-INFECTION-SCREENING, RF-CHL-ORGAN-DYSFUNCTION, RF-CHL-TRANSFORMATION-PROGRESSION

Skill catalog (3/16 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)

Last synced: 2026-05-04 · ctgov.

No active trials matched this scenario in ctgov.

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
ABVD (Adriamycin + Bleomycin + Vinblastine + Dacarbazine), 2-6 cycles (REG-ABVD)
✓ registered✓ covered₴-? — verify pathwayNSZU formulary
Aggressive plan
A+AVD (Brentuximab vedotin + Adriamycin + Vinblastine + Dacarbazine), 6 cycles (REG-A-AVD)
✓ registered✓ covered₴-? — verify pathwayNSZU formulary

Cost information is orientation. Verify with a specific pharmacy / foundation / trial site. Status updated: 2026-05-04.

plan_id: PLAN-BMA-CD30_CHL-V1 | version: 1 | generated: 2026-05-04T14:13:16.575478+00:00
Per FDA non-device CDS positioning (CHARTER §15): Outpatient oncology treatment planning to support tumor-board discussion. Not a medical device; not for autonomous clinical decision-making.
Per FDA non-device CDS positioning (CHARTER §15): Both treatment options below are presented for review. The engine's selection of a 'recommended' default does not constitute a clinical decision. Final treatment selection requires HCP judgment incorporating information not available to the system.
This document is an informational resource supporting tumor-board discussion (per CHARTER §11). It is not a system that makes clinical decisions. Every recommendation must be verified by the treating physician.