Lycopene and survival in patients with stage III colon cancer: Findings from CALGB (Alliance)/SWOG 80702.

S Seohyuk Lee (Beth Israel Deaconess Medical Center, Boston, MA) Q Qian Shi C Chao Ma P Pankaj Kumar (Department of Chemistry) F Felix Couture J J. Philip Kuebler (Columbus NCI Community Oncology Research Program, Columbus, OH) S Smitha S. Krishnamurthi (Cleveland Clinic, Cleveland, OH) B Benjamin R. Tan (Siteman Cancer Center, Washington University School of Medicine, St. Louis, MO) E Eileen M. O'Reilly (Memorial Sloan Kettering Cancer Center, New York City, NY) A Anthony F. Shields (Karmanos Cancer Institute, Wayne State University, Detroit, MI) E Edward L. Giovannucci Y Yasmin Mossavar-Rahmani (Albert Einstein College of Medicine, Bronx, New York, United States) J Jeffrey A. Meyerhardt E En Cheng (Department of Epidemiology and Population Health, Albert Einstein College of Medicine, Bronx, NY)

Abstract

3630 Background: Lycopene, a non-provitamin A carotenoid, has been reported to inhibit colon cancer development; however, its prognostic role after colon cancer diagnosis remains unknown. Given emerging evidence suggesting greater intake of lycopene-containing – particularly, tomato-based – foods may improve colon cancer prognosis, we assessed the association of postdiagnosis lycopene consumption with survival among 1666 patients (pts) with stage III colon cancer. Methods: Through an NCI-sponsored multicenter phase III adjuvant chemotherapy trial (CALGB/SWOG 80702; NCT01150045), we examined the consumption of total lycopene (dietary plus supplementation) and dietary lycopene as well as lycopene-containing foods (tomato-based foods plus other lycopene-containing foods) and tomato-based foods via validated food frequency questionnaires (FFQs) collected at 6 weeks after randomization (FFQ1) and again 14-16 months post-randomization (FFQ2). Lycopene-related exposures were calculated as time-varying measurements via cumulative averaging. Primary outcome was disease-free survival (DFS), defined as time from FFQ1 completion to colon cancer recurrence or death from any cause. Secondary outcomes were recurrence-free survival (RFS) and overall survival (OS). We estimated associations of lycopene-related exposures with survival via multivariable Cox proportional hazards regression. Results: In our cohort, pts with greater total lycopene intake tended to be slightly younger and of male sex and White race, have more left-sided tumors, and report higher caloric intake and physical activity engagement. Over median follow-up of 6.0 (IQR: 5.0-6.1) years, we observed 466 DFS, 395 RFS, and 300 OS events. Pts in the highest relative to lowest quintiles of total lycopene intake experienced significantly improved DFS (HR: 0.60 [95% CI: 0.44-0.83]; P trend =0.006), RFS (HR: 0.58 [95% CI: 0.41-0.82]; P trend =0.007), and OS (HR: 0.60 [95%CI: 0.40-0.89]; P trend =0.02). Similar findings were observed for dietary lycopene intake. Pts consuming >1 serving/day compared to 1 serving/week of all lycopene-containing foods did not experience significantly improved survival. However, when considering only tomato-based foods, we observed a trend toward improved survival (HR for DFS: 0.61 [95% CI: 0.38-0.96]; P trend =0.12). Conclusions: Greater lycopene consumption with or without supplementation was associated with lower risk of colon cancer recurrence and death which may be largely driven by tomato-based foods. Our findings may inform clinical nutrition recommendations for pts with colon cancer, with higher intake of tomato-based foods (>1 serving per day) potentially improving colon cancer survival. Future studies, especially interventional trials, are needed to validate our findings. Support: U10CA180821, U10CA180882, U24CA196171; Pfizer; https://acknowledgments.alliancefound.org.

Article Details

Volume / Issue Vol. 44, Issue 16_suppl
Published June 01, 2026
Pages 3630-3630
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (14)

S

Seohyuk Lee

Beth Israel Deaconess Medical Center, Boston, MA

Q

Qian Shi

C

Chao Ma

P

Pankaj Kumar

Department of Chemistry

F

Felix Couture

J

J. Philip Kuebler

Columbus NCI Community Oncology Research Program, Columbus, OH

S

Smitha S. Krishnamurthi

Cleveland Clinic, Cleveland, OH

B

Benjamin R. Tan

Siteman Cancer Center, Washington University School of Medicine, St. Louis, MO

E

Eileen M. O'Reilly

Memorial Sloan Kettering Cancer Center, New York City, NY

A

Anthony F. Shields

Karmanos Cancer Institute, Wayne State University, Detroit, MI

E

Edward L. Giovannucci

Y

Yasmin Mossavar-Rahmani

Albert Einstein College of Medicine, Bronx, New York, United States

J

Jeffrey A. Meyerhardt

E

En Cheng

Department of Epidemiology and Population Health, Albert Einstein College of Medicine, Bronx, NY