Structured exercise program following adjuvant chemotherapy for colon cancer: A cost-utility analysis of the CHALLENGE trial.

K Kelvin K. Chan (Odette Cancer Centre, Sunnybrook Health Sciences Centre, Toronto, ON, Canada) R Ryan W. Chu (University of Toronto, Toronto, ON, Canada) M Matthew C. Cheung (Sunnybrook Health Sciences Centre, Toronto, ON, Canada) K Kerry S. Courneya C Christopher J. O'Callaghan (Canadian Cancer Trials Group, Queen's University, Kingston, ON, Canada) J Janette L. Vardy (Faculty of Medicine and Health, University of Sydney, Sydney) S Sharlene Gill (BC Cancer–Vancouver, Vancouver, BC, Canada) C Christine Friedenreich (Departments of Oncology and Community Health Sciences, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada) R Rebecca KS Wong (Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada) H Haryana M. Dhillon (Faculty of Science, Psycho-Oncology Cooperative Research Group, School of Psychology, University of Sydney, Sydney) V Vicky Coyle (Queen's University Belfast, Belfast, United Kingdom) N Neil Sun Chua (Cross Cancer Institute, University of Alberta, Edmonton, AB, Canada) D Derek J. Jonker (Ottawa Hospital Research Institute, University of Ottawa, Ottawa) R Ralph M. Meyer (Department of Oncology, McMaster University, Hamilton, ON, Canada) S Shahid Ahmed J John Raymond Zalcberg (Department of Medical Oncology, Alfred Health and School of Public Health, Faculty of Medicine, Monash University, Melbourne, VIC, Australia) S Stephen John Clarke (University of Sydney, Sydney, NSW, Australia) P Patti O'Brien (Canadian Cancer Trials Group, Queen's University, Kingston, ON, Canada) D Dongsheng Tu (Canadian Cancer Trials Group, Queen’s University, Kingston, ON, Canada) C Christopher M. Booth (Department of Oncology, Queen’s University, Kingston, ON, Canada)

Abstract

3507 Background: The phase III CHALLENGE trial (CCTG CO.21) demonstrated improved disease-free and overall survival with a 3-year structured exercise program (SEP) compared with health education materials (HEM) in participants with stage III or high-risk stage II colon cancer that had undergone surgery and adjuvant chemotherapy. This study evaluated the cost-effectiveness of SEP versus HEM. Methods: A pre-specified economic evaluation was conducted using prospectively collected data from all trial participants (n = 889). The base case adopted the Canadian public healthcare payer perspective and included direct healthcare costs (cost categories available in Table 1), a 5-year time horizon, and a 1.5% discount rate. SF-36 trial data were mapped to SF-6D using a validated algorithm to calculate health utilities. Costs (2024 CAD) and effects measured as life-years (LYs) and quality-adjusted life-years (QALYs) were used to estimate an incremental cost-effectiveness ratio (ICER, $/life year gain (LYG)) and incremental cost-utility ratio (ICUR, $/QALY). Uncertainty was assessed via bootstrapping (n = 1,000). Notable scenario analyses included a 10-year horizon and a societal perspective capturing indirect costs from wages lost due to missed work, measured using a Work Productivity and Activity Impairment questionnaire. Results: In the base case, despite the up-front $4327 cost of the SEP intervention, the SEP was dominant over HEM (i.e less costly (−$179) and more effective (+0.06 LYs; +0.10 QALYs)). The SEP was dominant in 49% of bootstrap samples, while 79% met a $50,000 per QALY willingness-to-pay threshold. Major cost drivers in both groups were the costs of recurrence or new malignancy and anticancer therapy. Scenario analysis results were consistent with the base case analysis. The SEP remained dominant with a 10-year time horizon yielding greater cost savings ($-2,528) and more LYG (0.35) than the base case. From a societal perspective, the ICUR was $3,571/QALY, a highly cost-effective strategy. Conclusions: The SEP was less costly and more effective when compared with HEM. These data can inform health systems and payers as they look to implement SEP in routine models of care. Mean per participant costs, effects, and ICER/ ICUR for the base case analysis. SEP(n=445) HEM(n=444) Increment Cost of SEP sessions (including fixed start-up costs) ($) 4,327 0 4,327 Cost of hospitalization (pre- or without recurrence) ($) 3,593 3,092 501 Cost of recurrence or new malignancy (physicians, lab tests, drugs, hospitalizations, surgery, emergency room visits, home care)($) 12,732 15,772 -3,040 Cost of anticancer therapy ($) 12,660 14,582 -1,922 Cost of end-of-life care ($) 54 100 -46 Total cost ($) 33,367 33,546 -179 Total LYs 4.72 4.66 0.06 Total QALYs 3.84 3.75 0.09 ICER ($/LYG) and ICUR ($/QALY) Dominant* *SEP is less costly and more effective than HEM.

Article Details

Volume / Issue Vol. 44, Issue 16_suppl
Published June 01, 2026
Pages 3507-3507
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (20)

K

Kelvin K. Chan

Odette Cancer Centre, Sunnybrook Health Sciences Centre, Toronto, ON, Canada

R

Ryan W. Chu

University of Toronto, Toronto, ON, Canada

M

Matthew C. Cheung

Sunnybrook Health Sciences Centre, Toronto, ON, Canada

K

Kerry S. Courneya

C

Christopher J. O'Callaghan

Canadian Cancer Trials Group, Queen's University, Kingston, ON, Canada

J

Janette L. Vardy

Faculty of Medicine and Health, University of Sydney, Sydney

S

Sharlene Gill

BC Cancer–Vancouver, Vancouver, BC, Canada

C

Christine Friedenreich

Departments of Oncology and Community Health Sciences, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada

R

Rebecca KS Wong

Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada

H

Haryana M. Dhillon

Faculty of Science, Psycho-Oncology Cooperative Research Group, School of Psychology, University of Sydney, Sydney

V

Vicky Coyle

Queen's University Belfast, Belfast, United Kingdom

N

Neil Sun Chua

Cross Cancer Institute, University of Alberta, Edmonton, AB, Canada

D

Derek J. Jonker

Ottawa Hospital Research Institute, University of Ottawa, Ottawa

R

Ralph M. Meyer

Department of Oncology, McMaster University, Hamilton, ON, Canada

S

Shahid Ahmed

J

John Raymond Zalcberg

Department of Medical Oncology, Alfred Health and School of Public Health, Faculty of Medicine, Monash University, Melbourne, VIC, Australia

S

Stephen John Clarke

University of Sydney, Sydney, NSW, Australia

P

Patti O'Brien

Canadian Cancer Trials Group, Queen's University, Kingston, ON, Canada

D

Dongsheng Tu

Canadian Cancer Trials Group, Queen’s University, Kingston, ON, Canada

C

Christopher M. Booth

Department of Oncology, Queen’s University, Kingston, ON, Canada