数据分析

Hcc Meta Ai

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AI-assisted meta-analysis workflow for hepatocellular carcinoma comparative effectiveness research. Six-element prompt framework covering full pipeline from...

它能做什么

AI-assisted meta-analysis workflow for hepatocellular carcinoma comparative effectiveness research. Six-element prompt framework covering full pipeline from literature screening to data extraction. Published skill accompanying the validated methodology paper.

技能文档

HCC Meta-Analysis AI Skill

Overview

This skill implements a standardized, AI-assisted meta-analysis workflow for comparing treatment efficacy in hepatocellular carcinoma (HCC). It follows a six-element prompt architecture (Role–Objective–Skills–Constraints–Workflow–Output) validated across two independent clinical questions with three large language models.

The workflow covers the full meta-analysis pipeline:

  1. Literature screening (fuzzy → precise → supplementation)
  2. Full-text eligibility determination
  3. Newcastle–Ottawa Scale (NOS) quality appraisal
  4. Structured baseline data extraction
  5. Clinical outcome data extraction

Validation: Benchmarked against dual-independent manual review across two HCC projects with GPT-5.2, GPT-4o, and DeepSeek V3.1. Best-performing models achieved >95% accuracy at most stages with >80% total time reduction.

When to Use

  • Conducting a meta-analysis comparing two HCC treatments
  • Need rapid evidence synthesis for HCC therapeutic comparison
  • Want to standardize the AI-assisted review process across projects
  • Teaching or replicating the validated AI meta-analysis methodology

Six-Element Prompt Framework

Every prompt in this workflow follows a standardized six-element structure:

ElementPurposeExample
RoleDefines AI's academic persona"You are a clinical epidemiologist specializing in HCC..."
ObjectiveStates the specific task goal"Screen titles for studies comparing treatment A vs B..."
SkillsLists required capabilities"Identify medical terms, apply synonym rules, extract structured data"
ConstraintsSets methodological boundaries"Apply NOS scoring rules strictly; mark missing data as NA"
WorkflowSpecifies step-by-step execution"Read title → check for intervention terms → classify"
OutputDefines structured output format"Output as JSON table with fields: PMID, Decision, Reason"

Workflow Stages

Stage 1: Literature Screening

Three sub-stages with escalating cognitive demands:

  1. Fuzzy Screening — Title-level keyword matching

    • Batch 100 records per query
    • Check for presence of target disease + intervention terms
    • Template: scripts/01-fuzzy-screening.md
  2. Precise Screening — Abstract-level multi-constraint reasoning

    • Evaluate title + abstract against inclusion criteria
    • Requires comparison of two interventions with reported outcomes
    • Template: scripts/02-precise-screening.md
  3. Literature Supplementation — Citation tracing from full texts

    • Upload PDFs of included studies
    • Extract reference lists; flag potentially missed eligible studies
    • Template: scripts/03-literature-supplement.md

Stage 2: Full-Text Eligibility Determination

Full-text comprehension and multi-criteria decision-making:

  • Study population (primary HCC confirmed)
  • Direct comparison of two target treatments
  • ≥1 clinical outcome reported
  • Original study design (prospective/retrospective cohort, case-control, RCT)
  • Data separable by treatment group
  • Sample size ≥10
  • Template: scripts/04-eligibility.md

Stage 3: NOS Quality Appraisal

Structured scoring across three domains:

  • Selection (4 items, max 4 pts): representativeness, non-exposed cohort, exposure ascertainment, outcome absent at baseline
  • Comparability (1 item, max 2 pts): confounder control
  • Outcome (3 items, max 3 pts): assessment objectivity, follow-up duration, follow-up completeness
  • Template: scripts/05-nos-scoring.md

Stage 4: Baseline Data Extraction

Structured extraction of study characteristics and patient demographics:

  • Core fields: author, year, design, treatment groups, sample size, age, sex, tumor characteristics, follow-up, laboratory values
  • Topic-specific extensions (see references)
  • Template: scripts/06-baseline-extraction.md

Stage 5: Outcome Data Extraction

Structured extraction of clinical endpoints:

  • 1–5 year overall survival (OS), recurrence-free survival (RFS)
  • Local tumor progression, distant recurrence, technical success
  • Complication rates and subtypes
  • Template: scripts/07-outcome-extraction.md

Disease-Agnostic Design

The six-element scaffold is independent of specific diseases. To adapt this workflow for a different disease:

  1. Replace disease terminology in references/terminology.json
  2. Swap intervention names in each prompt template
  3. Adjust topic-specific extraction fields in baseline/outcome templates
  4. Keep the core logical structure intact

For HCC specifically, the pre-configured terminology and extraction fields in references/ are ready to use.

Platform

A web-based platform for deploying and sharing this workflow is available at: http://8.149.142.6/metaexp/

References

  • Full methodology: see accompanying manuscript
  • Supplementary prompt details: S1 (Project 1 prompts), S2 (Project 2 prompts)
  • Terminology database: references/terminology.json

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