Circulating T-cell receptor repertoire for cancer early detection
Liquid biopsy is a promising non-invasive technology that is capable of diagnosing cancer. However, current ctDNA-based approaches detect only a minority of early-stage disease. We set out to improve the sensitivity of liquid biopsy by harnessing tumor recognition by T cells through the sequencing of the circulating T-cell receptor repertoire. We studied a cohort of 463 patients with lung cancer (86% stage I) and 587 subjects without cancer using gDNA extracted from blood buffy coats. We performed TCR β chain sequencing to yield a median of 113,571 TCR clonotypes per sample and built a TCR sequence similarity graph to cluster clonotypes into TCR repertoire functional units (RFUs). The TCR frequencies of RFUs were tested for association with cancer status and RFUs with a statistically significant association were combined into a cancer score using a support vector machine model. The model was evaluated by 10-fold cross-validation and compared with a ctDNA panel of 237 mutation hotspots in 154 lung cancer driver genes and 17 cancer related protein biomarkers in 85 subjects. We identified 327 cancer-associated TCR RFUs with a false discovery rate (FDR) ≤ 0.1, including 157 enriched in cancer samples and 170 enriched in controls. Levels of 247/327 (76%) RFUs were correlated with the presence of an HLA allele at FDR ≤ 0.1 and tumor-infiltrating lymphocyte TCRs from multiple RFUs bound HLA presented tumor antigen peptides, suggesting antigen recognition as a driver of the cancer-RFU associations found. The RFU cancer score detected nearly 50% of stage I lung cancers at a specificity of 80% and boosted the sensitivity by up to 20 percentage points when added to ctDNA and circulating proteins in a multi-analyte cancer screening test. Overall, we show that circulating TCR repertoire functional unit analysis can complement established analytes to improve liquid biopsy sensitivity for early-stage cancer.
Authors
- Luis M. Montuenga (ORCID: https://orcid.org/0000-0002-8739-1387)
- Luis Seijó (ORCID: https://orcid.org/0000-0001-9344-728X)
- Andrea Pasquier
- Sophie Kivlehan (ORCID: https://orcid.org/0000-0002-5672-1697)
- Jeffrey A. Borgia (ORCID: https://orcid.org/0000-0002-1520-7966)
- Dennis Stephens
- Michelle Nahas
- Devin Champagne (ORCID: https://orcid.org/0000-0002-1958-7433)
- Hita Moudgalya (ORCID: https://orcid.org/0000-0001-5661-5571)
- Patrick H. Lizotte (ORCID: https://orcid.org/0000-0001-9510-0036)
- Christopher W. Seder (ORCID: https://orcid.org/0000-0002-4070-1245)
- Roman Yelensky (ORCID: https://orcid.org/0000-0002-5356-0111)
- Arantza Campo (ORCID: https://orcid.org/0000-0001-9700-4355)
- María Antonia Fortuño (ORCID: https://orcid.org/0000-0001-7088-7135)
- Markus Brown (ORCID: https://orcid.org/0000-0002-2069-0120)
- Iliana Gjeci
- Stephanie L. Korle (ORCID: https://orcid.org/0009-0001-7110-921X)
- Kate Froburg
- Amaneet Lochab
- Yilong Li (ORCID: https://orcid.org/0000-0002-3911-2830)
- María José Rodríguez (ORCID: https://orcid.org/0000-0003-0090-0642)
- Jasper Braun
- Raphael Bueno (ORCID: https://orcid.org/0000-0002-1258-8468)
- M.M. Ocón
- Emma Hintz
- Inés Luque-Vázquez
Institutions
- Brigham and Women's Hospital (US)
- Rush University Medical Center (US)
- National Vaccine and Serum Institute (CN)
- Navarre Institute of Health Research (ES)
- Dana-Farber Cancer Institute (US)
- Clinica Universidad de Navarra (ES)
- Detectogen (United States) (US)
- Rush University (US)
- Universidad de Navarra (ES)
- Universidad Europea de Madrid (ES)
Publication Details
- Journal
- npj Precision Oncology
- Published
- 2025-07-19
- DOI
- https://doi.org/10.1038/s41698-025-01036-y
- Citations
- 6
- Primary Topic
- Cancer Genomics and Diagnostics
- Type
- article
- Field-Weighted Citation Impact
- 5.62
Funders
- Universidad de Navarra
- Ministerio de Ciencia e Innovación
- Centro de Investigación Biomédica en Red de Cáncer
- European Regional Development Fund