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Continuous monitoring for blood-based and haematological cancers on active treatment, following disease-specific markers over time.
01Sentinel Blood
Sentinel Blood follows disease-specific molecular markers over time, so your team can see whether treatment is working and respond early if the picture changes.
It tracks condition-appropriate markers, for example NPM1, BCR-ABL1 or B-cell clonality signals where relevant, each result read against your baseline.
02
Establish your molecular starting point.
Monitoring on your chosen Track: 2, 4 or 6 per year.
The engine reads direction of travel, not one value.
A meaningful change triggers KPCIRC review and a plan.
03
Monitoring shows trends and can flag change early, but it does not replace your haematologist’s assessment or scheduled testing. No single result should be read in isolation, and decisions are made by your clinical team.
Being clear about our limits
| Term | What it means |
|---|---|
| ctDNA | Circulating tumour DNA, tumour fragments a blood test can read over time. |
| Resistance mutation | A new change that lets a cancer escape a treatment that was working. |
| Molecular progression | A rise in ctDNA signalling the cancer is advancing. |
| VAF | Variant allele frequency, how much of a mutation is present, tracked over time. |
| Serial monitoring | Repeat testing at intervals to watch the trend, not one snapshot. |
Sentinel Blood is a genomic (DNA-based) test for use by qualified healthcare professionals. It supports clinical judgement, it does not replace it, and it must be read alongside your full clinical history and applicable guidelines.
Regulatory status (India). Registration of our genomic tests as in-vitro diagnostic (IVD) medical devices with CDSCO is in progress, with the IVD class pending. Sequencing and variant calling are done by an accredited laboratory partner (CAP-accredited, ISO 15189) following ACMG/AMP/ASCO/CAP guidelines and a CE-IVD certified variant database. The OnKommon interpretation engine is provided for research and decision-support use. Marketing follows the Drugs and Magic Remedies (Objectionable Advertisements) Act, 1954.
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