Leads TRACERx, the study that follows lung cancers as they evolve, and showed how air pollution can trigger lung cancer without new mutations.
Charles Swanton is Deputy Clinical Director of The Francis Crick Institute and Chief Clinician of Cancer Research UK, and is involved in Cancer Grand Challenges. His specialisms are tumour evolution, lung cancer, circulating tumour DNA, and air pollution and cancer. He leads TRACERx, the programme that sequenced lung cancers over time to map clonal evolution, circulating tumour DNA dynamics and metastasis, using whole-exome and whole-genome sequencing and liquid biopsy. His Nature papers describe the evolution of non-small-cell lung cancer metastases in TRACERx and show how air pollutants promote lung adenocarcinoma through inflammation acting on pre-existing mutations rather than new ones. His Crick profile and PubMed listing are linked.
| Title | Journal | Year |
|---|---|---|
| The evolution of non-small cell lung cancer metastases in TRACERx | Nature | 2023 |
| Lung adenocarcinoma promotion by air pollutants | Nature | 2023 |
| Gerlinger: a single biopsy misses most of the mutations in a kidney tumour | New England Journal of Medicine | 2012 |
| TRACERx 421: the full-cohort picture of how lung cancer evolves and which subclones drive relapse | Nature | 2023 |
| TRACERx first 100: tracking how lung cancers evolve, and how chromosomal chaos predicts relapse | New England Journal of Medicine | 2017 |
For someone offered the test, these are the numbers that describe what a result means in an NHS population: about 1 in 100 tests came back positive each year, between 46 and 58 in 100 positives were cancer, and a negative result left about 1 in 100 with an undetected cancer within the year. The test found between a quarter and a third of all cancers diagnosed in a screening round, and about half to two thirds of the 12 cancer types it was designed to find. Whether finding them this way reduces late-stage diagnoses is the primary question, and this paper says only that the answer was no; the primary-endpoint paper had not appeared on Europe PMC by 23 September 2026.
It reframes air quality as cancer policy rather than respiratory policy, and it explains the shape of lung cancer in never-smokers: the mutations are common and mostly silent, and what differs is whether something inflames the tissue enough to let one of them grow.
Relapse after surgery is driven by particular subclones that can be identified in the primary tumour and tracked in blood, which argues for evolution-aware adjuvant strategies. The pollution finding reframes carcinogenesis: some agents promote already-mutant cells rather than causing mutations.
The foundation of minimal residual disease testing in lung cancer: a blood test that says a patient will relapse months before a scan does, and says which part of the tumour is doing it. Whether acting on that signal changes outcome is what the ctDNA-guided trials are for.
Lung cancers keep evolving after they form, and it is ongoing chromosomal instability rather than the number of mutations that best predicts who will relapse. This gives a rationale for targeting the earliest (clonal) drivers and neoantigens and for tracking evolution in blood after surgery.
A single biopsy is an incomplete picture of a patient's cancer. Truncal mutations shared by all cells (in kidney cancer, VHL) are the most reliable drug targets, whereas mutations in only some branches predict resistance. This is why liquid biopsy and multi-region sampling matter.
Shares Lung adenocarcinoma promotion by air pollutants, TRACERx 421: the full-cohort picture of how lung cancer evolves and which subclones drive relapse, The Francis Crick Institute, Non-small-cell lung cancer.
Shares The Francis Crick Institute, Cancer Research UK, Whole-exome & whole-genome sequencing, Non-small-cell lung cancer.
Shares Gerlinger: a single biopsy misses most of the mutations in a kidney tumour, Circulating tumour DNA (ctDNA), Liquid biopsy (ctDNA), Non-small-cell lung cancer.
Shares Cancer Grand Challenges, The Francis Crick Institute, Cancer Research UK.
Shares TRACERx 421: the full-cohort picture of how lung cancer evolves and which subclones drive relapse, Aneuploidy and chromosomal instability as the cause of cancer, TRACERx first 100: tracking how lung cancers evolve, and how chromosomal chaos predicts relapse, The Francis Crick Institute.
Shares Wellcome, The Francis Crick Institute.
Shares TRACERx 421: the full-cohort picture of how lung cancer evolves and which subclones drive relapse, Circulating tumour DNA (ctDNA), Liquid biopsy (ctDNA).
Shares The Francis Crick Institute, Cancer Research UK, Whole-exome & whole-genome sequencing.