Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

Poster display session: Biomarkers, Gynaecological cancers, Haematological malignancies, Immunotherapy of cancer, New diagnostic tools, NSCLC - early stage, locally advanced & metastatic, SCLC, Thoracic malignancies, Translational research

4284 - Microsatellite instability detection by targeted sequencing of cell-free DNA

Date

20 Oct 2018

Session

Poster display session: Biomarkers, Gynaecological cancers, Haematological malignancies, Immunotherapy of cancer, New diagnostic tools, NSCLC - early stage, locally advanced & metastatic, SCLC, Thoracic malignancies, Translational research

Topics

Targeted Therapy

Tumour Site

Presenters

Alex Artyomenko

Citation

Annals of Oncology (2018) 29 (suppl_8): viii400-viii441. 10.1093/annonc/mdy288

Authors

A. Artyomenko1, M. Sikora2, M. Lefterova3, V.M. Raymond4, D. Gavino3, C. Barbacioru1, C. Artieri3, E. Helman1, D. Chudova2, R.B. Lanman4, J. Odegaard5, J.A. Willis6, M. Fakih7, S. Kopetz8, A. Talasaz9

Author affiliations

  • 1 Bioinformatics, Guardant Health, 94063 - Redwood City/US
  • 2 Bioinformatics, Guardant Health, 94536 - Redwood City/US
  • 3 Medical Affairs, Guardant Health, 94536 - Redwood City/US
  • 4 Medical Affairs, Guardant Health, 94063 - Redwood City/US
  • 5 Guardant Health, Redwood City/US
  • 6 Oncology, The University of Texas MD Anderson Cancer Center, 77030 - Huston/US
  • 7 Medical Oncology Department, City of Hope, Duarte/US
  • 8 Department Of Gastrointestinal Medical Oncology, MD Anderson Cancer Center, 77030 - Houston/US
  • 9 Guardant Health, 94536 - Redwood City/US

Resources

Login to access the resources on OncologyPRO.

If you do not have an ESMO account, please create one for free.

Abstract 4284

Background

Microsatellite instability (MSI) is a guideline-recommended biomarker used in assessment of prognosis and treatment choices, including checkpoint inhibitors recently approved for cancers with MSI-high (MSI-H) status. Plasma-based next generation DNA sequencing (NGS) tests are increasingly used for comprehensive genomic profiling of cancer; however, sensitive methods to detect MSI status from cell-free DNA (cfDNA) are not available for clinical patient care. Additionally, the impact of variable tumor shedding on MSI detection has not been evaluated.

Methods

We developed an accurate method to assess MSI status using targeted sequencing of cfDNA using the Guardant360® clinical platform across a many cancer types, which allows broad coverage of simple repeats. For each microsatellite locus, the number of differently-sized repeats in experimental samples is quantified using a probabilistic log likelihood-based score designed to accurately discriminate biological signal derived from cfDNA fragments of somatic origin from noise arising from technical artifacts. Loci are considered unstable if the likelihood score is greater than a threshold computed from a cohort of normal samples. MSI status of a sample is determined by the presence of a minimum 5 unstable microsatellite loci among the 91 scored.

Results

We simulated MSI high (MSI-H) samples across a range of tumor fractions by combining data from 82 healthy donor samples with in silico spike-ins of differentially sized repeats. Simulated data demonstrates a sensitivity of 94% at 0.2% (limit of detection) tumor content for an expected specificity of 99.9% estimated from healthy donor samples. When applied to a prospective test set of 134 advanced cancer samples, this method demonstrated 98.5% (125/127) specificity and 86% sensitivity (6/7) relative to standard tissue PCR-based MSI assessment across a ctDNA range of 0.1%-15%.

Conclusions

Targeted sequencing of cfDNA data can enable highly accurate detection of MSI in cancer samples, even for samples with low tumor shedding. This novel approach enables non-invasive assessment of MSI status concurrent with comprehensive genomic profiling and allows potential access to immunotherapies for patients whose tumor types are not routinely tested for MSI.

Clinical trial identification

Legal entity responsible for the study

Guardant Health, Inc.

Funding

Guardant Health, Inc.

Editorial Acknowledgement

Disclosure

A. Artyomenko, M. Sikora, M. Lefterova, V.M. Raymond, D. Gavino, C. Barbacioru, C. Artieri, E. Helman, D. Chudova, R.B. Lanman, J. Odegaard, A. Talasaz: Employee: Guardant Health, Inc. All other authors have declared no conflicts of interest.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.