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Solid tumours · Liquid 523

Twin Liquid. Plasma-based ctDNA analysis for the solid-tumour pathway.

A 523-gene circulating tumour DNA panel from a blood sample, with hereditary testing included for germline filtering.

Overview

What this pathway is

OnKommon Twin · Twin Liquid

523-gene ctDNA panel from plasma. Hereditary testing included for germline filtering.

Tumours release small fragments of their DNA into the bloodstream, known as circulating tumour DNA (ctDNA). Twin Liquid analyses ctDNA from plasma using a 523-gene panel. Because it needs a blood sample rather than tissue, it can be useful when tissue is limited or difficult to obtain.

Intended audience and use

Who it is for

People with solid tumours for whom the treating team wants plasma-based testing — when tissue is limited, or for repeated reads over time.

Sample and testing pathway

Sample and what is generated

Sample
Plasma.
Information generated
Findings across the 523-gene panel. Hereditary testing is included, so inherited variants are filtered out before tumour findings are interpreted.

From result to Twin

How the information enters Twin

ctDNA findings feed the baseline Twin. SourceGuard is particularly relevant here, because plasma can contain inherited variants and variants from ageing blood cells as well as tumour DNA.

Analytical layers most relevant to this route

  1. 01 · Baseline — Day 0

    Integrate the data. Build the Twin.

  2. 02 · During months 0–6

    Review new findings inside the workflow.

  3. 03 · End of month 6

    Review the evidence. Set the next pathway.

  4. 04 · After six months

    Twin tracks

Strengths

Why this route

  • A blood draw instead of a biopsy.
  • DNA shed from across the tumour — not one biopsy site.
  • Hereditary testing built in, and SourceGuard separates tumour DNA from clonal haematopoiesis.

How every finding is interpreted, from detection to decision

Deliverables

What you receive

  • A structured Twin report in the five documented components: executive molecular summary, molecular findings, treatment options to evaluate, clinical-trial matches and a longitudinal view.
  • Review and sign-off by the treating oncologist, within the KPCIRC sign-off process.
  • Entry into the six-month Twin journey, with the option to continue into a Twin track afterwards.

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

Questions

Frequently asked questions

If my liquid biopsy shows nothing, does that mean there is no alteration?
Not necessarily. Some tumours release little DNA into the blood, so a negative result can be uninformative. Your oncologist may consider tissue testing.
What does 'hereditary testing for germline filtering' mean?
It separates inherited variants from tumour-acquired ones, so each finding is attributed correctly before it is interpreted.
Can a liquid biopsy replace a tissue biopsy?
Liquid and tissue testing answer overlapping but different questions. The choice is made by the treating team.

Other Twin pathways

Discuss Twin Liquid for a specific clinical question.

Continue the journey

The 21 analytical layers

Step inside every layer.

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