A randomized phase III trial of the impact of a structured exercise program on disease-free survival (DFS) in stage 3 or high-risk stage 2 colon cancer: Canadian Cancer Trials Group (CCTG) CO.21 (CHALLENGE).
Abstract
LBA3510 Background: Multiple observational studies have reported that post-diagnosis physical activity (PA) is associated with reduced recurrence rates in early-stage colon cancer but epidemiologic data is limited by confounding and reporting bias. CCTG CO.21 was designed to test the hypothesis that a meaningful increase in recreational PA after adjuvant therapy is achievable and will improve DFS in stage 3 or high-risk stage 2 colon cancer. Methods: CCTG CO.21 enrolled patients at 55 sites in 6 countries. Patients with resected stage 3 or high-risk stage 2 colon cancer who had received adjuvant chemotherapy were randomized to a structured exercise program (SEP) or health education materials (HEM). HEM participants received education materials promoting PA and healthy nutrition in addition to standard surveillance. SEP participants worked with a PA consultant who delivered an exercise intervention using behavior change methodology over 3 years. The SEP goal was to increase recreational PA by at least 10 MET-hours/week from baseline during the first 6 months and sustain this for 3 years. Participants chose the type, frequency, intensity and duration of aerobic exercise. The primary endpoint is DFS compared by a stratified log-rank test performed on an intention-to-treat basis. Secondary endpoints include overall survival (OS) and patient-reported outcomes (SF-36 physical function scale was primary PRO). Results: Between 2009 and 2024,889 participants were randomized to SEP (n=445) or HEM (n=444); 51% female, median age 61 years, 90% stage 3 disease. Compared to HEM, SEP resulted in statistically significant improvements in recreational PA, predicted VO2max, and 6-minute walk distance, all maintained over the 3-year intervention period. With a median follow-up of 7.9 years, 224 DFS events (93 in SEP and 131 in HEM) and 107 deaths (41 in SEP and 66 in HEM) were observed. 5-year DFS was 80% in SEP and 74% in HEM (HR 0.72; 95% CI 0.55-0.94; p=0.017). 8-year OS was 90% in SEP and 83% in HEM (HR=0.63; 95% CI=0.43-0.94; p=0.022). SF-36 physical function was substantially improved with SEP at 6 months (mean change scores 7.42 vs 1.10, p<0.001) and was sustained to 24 months. In the safety analysis, 19% (79/428) of patients on SEP reported any grade of musculoskeletal adverse event (MSK AE) over the course of the study, compared to 12% (50/433) on HEM. 10% (8/79) of MSK AE on SEP were considered to be related to participation in the PA program. Conclusions: Inpatients with stage 3 and high-risk stage 2 colon cancer, a 3-year structured exercise program initiated shortly after completion of adjuvant chemotherapy improves DFS, OS, patient-reported physical functioning, and health-related fitness. Health systems should incorporate structured exercise programs as standard of care for this patient population. Clinical trial information: NCT00819208 .
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (20)
Christopher M. Booth
Department of Oncology, Queen’s University, Kingston, ON, Canada
Janette L. Vardy
Faculty of Medicine and Health, University of Sydney, Sydney
Christopher J. O'Callaghan
Canadian Cancer Trials Group, Queen's University, Kingston, ON, Canada
Sharlene Gill
BC Cancer–Vancouver, Vancouver, BC, Canada
Christine Friedenreich
Departments of Oncology and Community Health Sciences, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada
Rebecca KS Wong
Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada
Haryana M. Dhillon
Faculty of Science, Psycho-Oncology Cooperative Research Group, School of Psychology, University of Sydney, Sydney
Victoria Coyle
Queen’s University Belfast, Belfast, United Kingdom
Neil Sun Chua
Cross Cancer Institute, University of Alberta, Edmonton, AB, Canada
Derek J. Jonker
Ottawa Hospital Research Institute, University of Ottawa, Ottawa
Philip James Beale
Concord Cancer Centre, Concord Hospital, Concord, NSW, Australia
Kamal Haider
Saskatoon Cancer Centre, University of Saskatchewan, Saskatoon, Canada
Patricia A. Tang
Arthur J.E. Child Comprehensive Cancer Centre, University of Calgary, Calgary, AB, Canada
Tony Bonaventura
Newcastle Private Hospital, New Lambton Heights, NSW, Australia
Ralph Wong
CancerCare Manitoba, St. Boniface General Hospital, Winnipeg, Canada
Howard J. Lim
BC Cancer–Vancouver, Vancouver, BC, Canada
Matthew E. Burge
Royal Brisbane and Women’s Hospital, Herston, QLD, Australia
Patti O'Brien
Canadian Cancer Trials Group, Queen's University, Kingston, ON, Canada
Dongsheng Tu
Canadian Cancer Trials Group, Queen’s University, Kingston, ON, Canada
Kerry S. Courneya