OnCo
technologiesTechnologyStandard of care

NGS-based MRD (clonoSEQ and molecular MRD)

Sequencing the unique genetic barcode of a patient's leukaemia to find one cancer cell in a million.

clonoSEQ (Adaptive Biotechnologies) tracks clonal IGH/TCR rearrangements at 10^-6 and is FDA-cleared for ALL, myeloma, and CLL. In AML, quantitative PCR of NPM1 or core-binding-factor fusion transcripts and error-corrected NGS of persistent mutations (excluding DNMT3A/TET2/ASXL1) define molecular MRD per ELN 2021. MRD status now drives transplant decisions in AML, blinatumomab use in ALL, and fixed-duration versus continuous therapy debates in CLL.

Generic schematic · not to scale · placeholder for the diagnostics front
Molecular read-out

How it works

The assay deep-sequences a patient-specific clonotype or mutation with error correction.

Strengths
  • 10^-5 to 10^-6 sensitivity
  • Blood-based monitoring in many settings
Limitations
  • Requires a baseline sample to identify the clone
  • Persisting pre-leukaemic clones (CHIP) confound AML MRD

Latest papers

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Literature trend9 papers in the last 12 months+50% vs prior 12How this is computed
Latest papers · live from Europe PMC
Open in Europe PMC

Query for this technology: (TITLE:"NGS-based MRD" OR ABSTRACT:"NGS-based MRD" OR TITLE:"clonoSEQ and molecular MRD" OR ABSTRACT:"clonoSEQ and molecular MRD") AND (cancer OR tumor OR tumour OR oncology OR carcinoma OR lymphoma OR leukemia OR leukaemia OR myeloma OR sarcoma OR melanoma OR glioma). Results are unfiltered search hits about NGS-based MRD (clonoSEQ and molecular MRD), not a curated reading list.

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