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Layer 13 of 21 · Clinical integration

Staging & Prognostic Models Stage, risk models and outcome estimates.

Staging and risk information shapes almost every treatment conversation. This layer is intended to summarise the staging and prognosis-related information applicable to the case, with the method and its source stated.

Why it's needed

What staging or prognosis-related information is available and applicable to the case?

The applicable staging and risk methods, named and sourced.

What it draws on

3 of 8 evidence domains.

Clinical contextMolecular & genomicImaging integrationClinical stage, relevant molecular risk markers and imaging findings.

What it produces

Staging and risk or prognosis context with method and source attribution.

Describe the staging and prognostic methods that are actually implemented and their evidence base.

Why it's essential

Layer 13 of 21.

Frames the executive summary and the context in which treatment options are considered.

1 · What it does

What Staging & Prognostic Models does

Staging and risk information shapes almost every treatment conversation. This layer is intended to summarise the staging and prognosis-related information applicable to the case, with the method and its source stated.

2 · Scientific question

The question it addresses

What staging or prognosis-related information is available and applicable to the case?

Intended function

Describe the staging and prognostic methods that are actually implemented and their evidence base.

3 · Data inputs and required context

What it draws on

  • 03 Clinical context
  • 01 Molecular & genomic
  • 04 Imaging integration

Clinical stage, relevant molecular risk markers and imaging findings.

4 · Scientific basis

The science behind it

Scientific basis

Staging systems and disease-specific risk scores are developed and validated in particular populations, and some risk scores incorporate molecular findings, particularly in blood cancers. Applying a model outside the population in which it was validated reduces its reliability.

5 · Output and evidence sources

What it produces

Main output

Staging and risk or prognosis context with method and source attribution.

Output type

  • Evidence-linked interpretation. Connects a finding to published or curated evidence, which has a source and a date.
  • Clinical-context integration. Depends on clinical information supplied by the treating team.

6 · Why it\u2019s essential

How it powers the Twin

Frames the executive summary and the context in which treatment options are considered.

Capability

Understand

Bring molecular findings and relevant clinical context into a structured view.

7 · Why it\u2019s needed

What it changes — for doctors, patients and researchers

Clinicians

The applicable staging and risk methods, named and sourced.

Doctor & Clinical Team

Patients & caregivers

Prognosis is a conversation to have with the oncologist; population estimates are not personal predictions.

Patient & Caregiver

Researchers

Consistent staging annotation across cases.

Industry & Research

8 · Dependencies and limitations

Limitations

    9 · Review and uncertainty

    How the output is handled

    Output status

    An AI-assisted analytical output presented as structured findings for clinician review. It becomes part of a report only after the treating oncologist has reviewed and signed it.

    How uncertainty is communicated

    Each estimate names its model, the population it was validated in, and whether the case falls within that population.

    10 · Claim boundary

    What this layer does not establish

    It does not predict an individual patient's outcome or survival.

    The treating oncologist owns every decision. Every Twin report is reviewed and signed by the treating oncologist, then taken to KPCIRC's Molecular Tumour Board.

    KPCIRC sign-off process

    Continue the journey

    Longitudinal monitoring

    Every change goes in.

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