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myeloma-mrd-agent

myeloma-mrd-agent,来自 FreedomIntelligence/OpenClaw-Medical-Skills 的 agent 技能。

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This file is part of the "Universal Biomedical Skills" project.

Copyright (c) 2026 MD BABU MIA, PhD <md.babu.mia@mssm.edu>

All Rights Reserved.

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This code is proprietary and confidential.

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name: 'myeloma-mrd-agent'

description: 'AI-powered minimal residual disease (MRD) analysis for multiple myeloma using next-generation flow cytometry, NGS, and mass spectrometry approaches.'

measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes.

allowed-tools:

  • read_file
  • run_shell_command

Myeloma MRD Agent

The Myeloma MRD Agent provides comprehensive AI-driven minimal residual disease assessment for multiple myeloma. It integrates next-generation flow cytometry (NGF), NGS-based clonotype tracking, and mass spectrometry M-protein detection for ultra-sensitive MRD monitoring.

When to Use This Skill

  • When assessing MRD status in multiple myeloma patients post-treatment.
  • To select optimal MRD testing modality (NGF vs NGS vs MS).
  • For predicting progression-free survival based on MRD kinetics.
  • When integrating MRD with other response criteria (IMWG).
  • To guide treatment intensification or de-escalation decisions.

Core Capabilities

  1. NGF Analysis: AI-enhanced next-generation flow cytometry for MRD detection at 10^-5 to 10^-6 sensitivity.
  1. NGS Clonotype Tracking: Analyze IGH/IGK/IGL rearrangements for molecular MRD.
  1. Mass Spectrometry: MALDI-TOF or LC-MS/MS for M-protein detection.
  1. Multi-Modal Integration: Combine modalities for comprehensive MRD assessment.
  1. Kinetic Modeling: Track MRD dynamics and predict outcomes.
  1. Response Classification: Apply IMWG MRD criteria.

MRD Detection Methods

| Method | Sensitivity | Sample | Advantages |

|--------|-------------|--------|------------|

| NGF (EuroFlow) | 10^-5 to 10^-6 | BM | Standardized, fast |

| NGS (clonoSEQ) | 10^-6 | BM | Ultra-sensitive |

| ASO-qPCR | 10^-5 | BM | Quantitative |

| PET-CT | N/A | Whole body | Extramedullary |

| MS (MALDI/LC-MS) | 10^-5 | Serum | Non-invasive |

IMWG MRD Response Criteria

| Category | Definition |

|----------|------------|

| MRD-negative (10^-5) | No clonal plasma cells by NGF or NGS at 10^-5 |

| MRD-negative (10^-6) | No clonal plasma cells at 10^-6 sensitivity |

| Sustained MRD-neg | MRD-neg confirmed ≥1 year apart |

| Flow MRD-neg | NGF negative, sensitivity ≥10^-5 |

| Sequencing MRD-neg | NGS negative, sensitivity ≥10^-5 |

Workflow

  1. Input: Flow cytometry FCS files, NGS clonotype data, M-protein MS data, clinical parameters.
  1. NGF Analysis: AI-assisted gating and aberrant plasma cell identification.
  1. NGS Analysis: Clonotype frequency calculation and threshold application.
  1. MS Analysis: M-protein peak detection and quantification.
  1. Integration: Combine multi-modal MRD data.
  1. Kinetics: Model MRD trajectory and predict outcomes.
  1. Output: MRD status, response category, prognostic estimate.

Example Usage

User: "Analyze MRD status for this myeloma patient using flow and NGS data."

Agent Action:

python3 Skills/Hematology/Myeloma_MRD_Agent/myeloma_mrd.py \
    --flow_fcs bone_marrow_ngf.fcs \
    --ngs_clonotype clonoseq_results.json \
    --ms_mprotein maldi_spectrum.csv \
    --baseline_clone diagnosis_clone.json \
    --treatment_phase post_consolidation \
    --output mrd_report.json

NGF Panel (EuroFlow-Based)

Tube 1: CD138/CD38/CD45/CD19/CD56/CD27/CD81/CD117

Aberrant Plasma Cell Phenotype:

  • CD138+, CD38++
  • CD19- or dim (normal PC: CD19+)
  • CD56+ (normal PC: CD56-)
  • CD45- or dim (normal PC: CD45+)
  • CD27- or dim
  • CD117+ (often aberrant)

AI-Assisted Flow Cytometry

Automated Gating:

  • CNN-based plasma cell identification
  • Aberrant vs normal PC discrimination
  • Consistent quantification across samples

Quality Control:

  • Sample adequacy assessment
  • Hemodilution detection
  • Event count validation

NGS Clonotype Analysis

Process:

  1. Identify dominant clone at diagnosis (IGH/IGK/IGL)
  2. Design clone-specific assay or use multiplex (clonoSEQ)
  3. Track clonal frequency in follow-up samples
  4. Apply MRD threshold (typically 10^-5 or 10^-6)

Considerations:

  • Clonal evolution may affect tracking
  • Biclonal disease requires tracking both
  • IGK/IGL backup if IGH fails

Prognostic Significance

| MRD Status | PFS HR | OS HR |

|------------|--------|-------|

| MRD-neg (10^-5) | 0.35-0.45 | 0.40-0.50 |

| MRD-neg (10^-6) | 0.25-0.35 | 0.30-0.40 |

| Sustained MRD-neg | 0.20-0.30 | 0.25-0.35 |

Clinical Decision Support

MRD-Guided Treatment:

  • De-escalation in sustained MRD-neg
  • Intensification if MRD conversion
  • Maintenance duration decisions

Monitoring Frequency:

  • Post-induction
  • Post-consolidation
  • Post-transplant (Day +100)
  • Every 6-12 months on maintenance

Prerequisites

  • Python 3.10+
  • FlowJo or equivalent for FCS files
  • NGS analysis pipelines
  • Mass spectrometry processing tools

Related Skills

  • Flow_Cytometry_AI - For general flow analysis
  • Multiple_Myeloma_AI - For disease-specific analysis
  • Liquid_Biopsy_Analytics_Agent - For ctDNA approaches

Emerging Methods

  1. Circulating tumor cells: Blood-based PC detection
  2. Cell-free DNA: Myeloma-specific mutations
  3. Imaging: PET/MRI for extramedullary disease
  4. Serum-based NGS: M-protein sequencing

Author

AI Group - Biomedical AI Platform

<!-- AUTHOR_SIGNATURE: 9a7f3c2e-MD-BABU-MIA-2026-MSSM-SECURE -->

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