OnCo
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CHALLENGE: a structured exercise programme after chemotherapy improves survival in colon cancer

In CHALLENGE, three years of supervised, goal-based exercise after adjuvant chemotherapy for colon cancer reduced recurrence or death by 28% and deaths by 37%, the first randomised proof that exercise itself improves cancer survival.

CHALLENGE (CCTG CO.21) randomised 889 patients with resected stage III or high-risk stage II colon cancer who had completed adjuvant chemotherapy to a 3-year structured exercise programme (behavioural support and supervised sessions, targeting an increase of at least 10 MET-hours per week) or to health-education materials alone. The primary endpoint was disease-free survival.

After a median follow-up of nearly 8 years, 5-year DFS was 80.3% with exercise versus 73.9% with education (HR 0.72). Eight-year overall survival was 90.3% versus 83.2% (HR 0.63). Physical functioning improved and musculoskeletal adverse events were more common in the exercise arm.

This is the first phase 3 trial to show that an exercise intervention, rather than exercise as a correlate, lengthens survival in cancer.

Randomised controlled trialChanged practice889 participants
Authors
Courneya KS, Vardy JL, O'Callaghan CJ, et al. (Canadian Cancer Trials Group CO.21)
What it found
  • Five-year disease-free survival 80.3% vs 73.9% (HR 0.72, 95% CI 0.55-0.94)
  • Eight-year overall survival 90.3% vs 83.2% (HR 0.63, 95% CI 0.43-0.94)
  • Median follow-up 7.9 years across 55 centres in Canada, Australia, the UK, France, Israel and the US
  • Musculoskeletal adverse events 18.5% vs 11.5%; the programme was delivered by physical activity consultants over 3 years
What it means

For colon cancer survivors, a prescribed, supported exercise programme is now an evidence-based treatment with a survival benefit comparable to many drugs. Health systems will need to fund exercise consultants as they fund chemotherapy. The trial does not tell us whether unsupervised advice achieves the same.

Be careful
  • The intervention was intensive (behavioural support for 3 years); uptake and cost in routine care are untested
  • Participants were fit enough to enrol and motivated; benefit in frail or sedentary populations is unproven
  • Open-label; DFS assessment could be influenced by differential surveillance
  • Recruitment took 15 years, so adjuvant regimens evolved during the trial

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