Media release

From: Peter MacCallum Cancer Centre

An international study led by a Peter Mac oncologist shows that a simple blood test could change how doctors decide which patients with colon cancer need chemotherapy.

Professor Jeanne Tie led the DYNAMIC-III clinical trial with the findings just presented at the European Society for Medical Oncology (ESMO) Congress in Germany, and simultaneously published in Nature Medicine.

The study found testing for tiny fragments of cancer DNA in the bloodstream, known as circulating tumour DNA (or ctDNA), can reveal if cancer is present after surgery, and help tailor treatment accordingly.

More than 1,000 people with stage III colon cancer across Australia, New Zealand and Canada took part in the study and all had blood taken about six weeks after surgery to remove their primary colon cancer.

If no ctDNA was detected, patients were considered "low-risk"; if ctDNA was present, they were "high-risk". Participants were randomly assigned to receive either standard chemotherapy or treatment guided by their ctDNA results.

Professor Tie, who is also a Senior Clinical Research Fellow at WEHI, said the findings show how ctDNA could bring true precision medicine to colon cancer.

“ctDNA is a powerful tool that can help guide treatment choices and identify which patients might safely receive less intensive treatment and those who might need to seek alternative options," she said.

“Right now, we give most stage III patients the same chemotherapy, but ctDNA testing can help tailor treatment based on individual risk.

“For some patients, this means a less intensive approach may be just as effective while reducing unnecessary toxicity from chemotherapy such as oxaliplatin and improving their quality of life.

“The DYNAMIC-III study shows that a blood test can help to give patients more personalised, risk-adapted chemotherapy by identifying who may benefit from full-intensity chemotherapy and who can safely receive a reduced regimen.”

Outcomes were excellent among the patients identified as low risk based on their ctDNA levels, with 87 per cent remaining cancer-free three years after surgery.

“These patients were able to safely receive less chemotherapy, leading to fewer hospitalisations and a reduction in side-effects such as nerve damage, with only slightly lower cancer free survival,” Professor Tie explained.

By contrast, patients whose ctDNA remained detectable after surgery had a much higher risk of recurrence - only about half remained cancer-free at three years, and the risk worsened as ctDNA levels rose.

For this group, receiving more intensive chemotherapy did not improve results, suggesting new treatment approaches are needed.

This study was in collaboration with the Canadian Cancer Trials Group (CCTG), Australasian GI Trials Group (AGITG) and WEHI.

Dr Jonathan Loree, DYNAMIC-III Canadian Study Chair and CCTG Senior Investigator, said they were thrilled to work with Australian collaborators on such an important trial.

“This study provides the best available prospective evidence of the prognostic value of ctDNA in selecting adjuvant chemotherapy for patients with resected stage III colon cancer,” Dr Loree said.

“Its results are crucial as we build the evidence needed to move ctDNA into the clinic.”

Colon cancer is the fourth most common cancer in Australia with more than 15,000 people diagnosed in 2024.

The paper in Nature Medicine is titled "Circulating tumor DNA-guided adjuvant therapy in locally advanced colon cancer: the randomized phase 2/3 DYNAMIC-III trial" and you can read it here.

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For more information contact the Peter Mac Communications team on 0417 123 048.

About Peter Mac

Peter MacCallum Cancer Centre is a world leading cancer research, education and treatment centre and Australia’s only public health service dedicated to caring for people affected by cancer.